Sunitinib inhibits lymphatic endothelial cell functions and lymph node metastasis in a breast cancer model through inhibition of vascular endothelial growth factor receptor 3
Identifieur interne : 003C43 ( Pmc/Corpus ); précédent : 003C42; suivant : 003C44Sunitinib inhibits lymphatic endothelial cell functions and lymph node metastasis in a breast cancer model through inhibition of vascular endothelial growth factor receptor 3
Auteurs : Yasuo Kodera ; Yasufumi Katanasaka ; Yuka Kitamura ; Hitoshi Tsuda ; Kazuto Nishio ; Tomohide Tamura ; Fumiaki KoizumiSource :
- Breast Cancer Research : BCR [ 1465-5411 ] ; 2011.
Abstract
Metastasis is a common event and the main cause of death in cancer patients. Lymphangiogenesis refers to the formation of new lymphatic vessels and is thought to be involved in the development of metastasis. Sunitinib is a multi-kinase inhibitor that blocks receptor tyrosine kinase activity, including that of vascular endothelial growth factor receptors (VEGFRs). Although sunitinib is a clinically available angiogenesis inhibitor, its effects on lymphangiogenesis and lymph node metastasis remain unclear. The purpose of this study was to investigate the effects of sunitinib on vascular endothelial growth factor receptor 3 (VEGFR-3) and a related event, lymphangiogenesis.
The effects of sunitinib on the degree of phosphorylation of VEGFR-2/3 and other signaling molecules was examined in lymphatic endothelial cells (LECs) treated with the drug; VEGF-induced LEC growth, migration, and tube formation were also examined. For the
First, in human LECs, sunitinib blocked both VEGFR-2 and VEGFR-3 phosphorylation induced by VEGF-C or VEGF-D, and abrogated the activation of the downstream molecules extracellular signal-regulated kinase 1/2 (ERK1/2) and Akt. Furthermore, sunitinib attenuated the cell-proliferation activity induced by VEGF-C/D and prevented VEGF-C-induced migration and tube formation of the LECs; however, anti-VEGFR2 treatment shows only a partial effect on the growth and functions of the LECs. We used a breast cancer cell line expressing luciferase as a metastatic cancer model. Sunitinib treatment (40 mg/kg/day) inhibited the growth of the primary tumor transplanted in the mammary fat pad of the mice and significantly reduced the number of blood and lymphatic vessels in the tumor. Furthermore, the development of axillary lymph node metastasis, detected by bioluminescent imaging, was markedly suppressed. This effect of sunitinib was more potent than that of DC101, an anti-mouse VEGFR-2 antibody.
The results suggest that sunitinib might be beneficial for the treatment of breast cancer by suppressing lymphangiogenesis and lymph node metastasis, through inhibition, particularly important, of VEGFR-3.
Url:
DOI: 10.1186/bcr2903
PubMed: 21693010
PubMed Central: 3218955
Links to Exploration step
PMC:3218955Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Sunitinib inhibits lymphatic endothelial cell functions and lymph node metastasis in a breast cancer model through inhibition of vascular endothelial growth factor receptor 3</title><author><name sortKey="Kodera, Yasuo" sort="Kodera, Yasuo" uniqKey="Kodera Y" first="Yasuo" last="Kodera">Yasuo Kodera</name><affiliation><nlm:aff id="I1">Shien-Lab, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation><affiliation><nlm:aff id="I2">Department of Genome Biology, Kinki University Faculty of Medicine, 377-2 Ohno-higashi, Osaka-Sayama, Osaka 589-8511, Japan</nlm:aff></affiliation></author><author><name sortKey="Katanasaka, Yasufumi" sort="Katanasaka, Yasufumi" uniqKey="Katanasaka Y" first="Yasufumi" last="Katanasaka">Yasufumi Katanasaka</name><affiliation><nlm:aff id="I3">Division of Molecular Medicine, Graduate School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan</nlm:aff></affiliation></author><author><name sortKey="Kitamura, Yuka" sort="Kitamura, Yuka" uniqKey="Kitamura Y" first="Yuka" last="Kitamura">Yuka Kitamura</name><affiliation><nlm:aff id="I1">Shien-Lab, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation></author><author><name sortKey="Tsuda, Hitoshi" sort="Tsuda, Hitoshi" uniqKey="Tsuda H" first="Hitoshi" last="Tsuda">Hitoshi Tsuda</name><affiliation><nlm:aff id="I4">Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation></author><author><name sortKey="Nishio, Kazuto" sort="Nishio, Kazuto" uniqKey="Nishio K" first="Kazuto" last="Nishio">Kazuto Nishio</name><affiliation><nlm:aff id="I2">Department of Genome Biology, Kinki University Faculty of Medicine, 377-2 Ohno-higashi, Osaka-Sayama, Osaka 589-8511, Japan</nlm:aff></affiliation></author><author><name sortKey="Tamura, Tomohide" sort="Tamura, Tomohide" uniqKey="Tamura T" first="Tomohide" last="Tamura">Tomohide Tamura</name><affiliation><nlm:aff id="I5">Department of Thoracic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation></author><author><name sortKey="Koizumi, Fumiaki" sort="Koizumi, Fumiaki" uniqKey="Koizumi F" first="Fumiaki" last="Koizumi">Fumiaki Koizumi</name><affiliation><nlm:aff id="I1">Shien-Lab, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">21693010</idno><idno type="pmc">3218955</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218955</idno><idno type="RBID">PMC:3218955</idno><idno type="doi">10.1186/bcr2903</idno><date when="2011">2011</date><idno type="wicri:Area/Pmc/Corpus">003C43</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">003C43</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Sunitinib inhibits lymphatic endothelial cell functions and lymph node metastasis in a breast cancer model through inhibition of vascular endothelial growth factor receptor 3</title><author><name sortKey="Kodera, Yasuo" sort="Kodera, Yasuo" uniqKey="Kodera Y" first="Yasuo" last="Kodera">Yasuo Kodera</name><affiliation><nlm:aff id="I1">Shien-Lab, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation><affiliation><nlm:aff id="I2">Department of Genome Biology, Kinki University Faculty of Medicine, 377-2 Ohno-higashi, Osaka-Sayama, Osaka 589-8511, Japan</nlm:aff></affiliation></author><author><name sortKey="Katanasaka, Yasufumi" sort="Katanasaka, Yasufumi" uniqKey="Katanasaka Y" first="Yasufumi" last="Katanasaka">Yasufumi Katanasaka</name><affiliation><nlm:aff id="I3">Division of Molecular Medicine, Graduate School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan</nlm:aff></affiliation></author><author><name sortKey="Kitamura, Yuka" sort="Kitamura, Yuka" uniqKey="Kitamura Y" first="Yuka" last="Kitamura">Yuka Kitamura</name><affiliation><nlm:aff id="I1">Shien-Lab, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation></author><author><name sortKey="Tsuda, Hitoshi" sort="Tsuda, Hitoshi" uniqKey="Tsuda H" first="Hitoshi" last="Tsuda">Hitoshi Tsuda</name><affiliation><nlm:aff id="I4">Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation></author><author><name sortKey="Nishio, Kazuto" sort="Nishio, Kazuto" uniqKey="Nishio K" first="Kazuto" last="Nishio">Kazuto Nishio</name><affiliation><nlm:aff id="I2">Department of Genome Biology, Kinki University Faculty of Medicine, 377-2 Ohno-higashi, Osaka-Sayama, Osaka 589-8511, Japan</nlm:aff></affiliation></author><author><name sortKey="Tamura, Tomohide" sort="Tamura, Tomohide" uniqKey="Tamura T" first="Tomohide" last="Tamura">Tomohide Tamura</name><affiliation><nlm:aff id="I5">Department of Thoracic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation></author><author><name sortKey="Koizumi, Fumiaki" sort="Koizumi, Fumiaki" uniqKey="Koizumi F" first="Fumiaki" last="Koizumi">Fumiaki Koizumi</name><affiliation><nlm:aff id="I1">Shien-Lab, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</nlm:aff></affiliation></author></analytic><series><title level="j">Breast Cancer Research : BCR</title><idno type="ISSN">1465-5411</idno><idno type="eISSN">1465-542X</idno><imprint><date when="2011">2011</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Introduction</title><p>Metastasis is a common event and the main cause of death in cancer patients. Lymphangiogenesis refers to the formation of new lymphatic vessels and is thought to be involved in the development of metastasis. Sunitinib is a multi-kinase inhibitor that blocks receptor tyrosine kinase activity, including that of vascular endothelial growth factor receptors (VEGFRs). Although sunitinib is a clinically available angiogenesis inhibitor, its effects on lymphangiogenesis and lymph node metastasis remain unclear. The purpose of this study was to investigate the effects of sunitinib on vascular endothelial growth factor receptor 3 (VEGFR-3) and a related event, lymphangiogenesis.</p></sec><sec><title>Methods</title><p>The effects of sunitinib on the degree of phosphorylation of VEGFR-2/3 and other signaling molecules was examined in lymphatic endothelial cells (LECs) treated with the drug; VEGF-induced LEC growth, migration, and tube formation were also examined. For the <italic>in vivo </italic>study, luciferase-expressing breast cancer cells were transplanted into mammary fat pads of mice; the microvessel and lymphatic vessel density was then measured after treatment with sunitinib and anti-VEGFR-2 antibody.</p></sec><sec><title>Results</title><p>First, in human LECs, sunitinib blocked both VEGFR-2 and VEGFR-3 phosphorylation induced by VEGF-C or VEGF-D, and abrogated the activation of the downstream molecules extracellular signal-regulated kinase 1/2 (ERK1/2) and Akt. Furthermore, sunitinib attenuated the cell-proliferation activity induced by VEGF-C/D and prevented VEGF-C-induced migration and tube formation of the LECs; however, anti-VEGFR2 treatment shows only a partial effect on the growth and functions of the LECs. We used a breast cancer cell line expressing luciferase as a metastatic cancer model. Sunitinib treatment (40 mg/kg/day) inhibited the growth of the primary tumor transplanted in the mammary fat pad of the mice and significantly reduced the number of blood and lymphatic vessels in the tumor. Furthermore, the development of axillary lymph node metastasis, detected by bioluminescent imaging, was markedly suppressed. This effect of sunitinib was more potent than that of DC101, an anti-mouse VEGFR-2 antibody.</p></sec><sec><title>Conclusions</title><p>The results suggest that sunitinib might be beneficial for the treatment of breast cancer by suppressing lymphangiogenesis and lymph node metastasis, through inhibition, particularly important, of VEGFR-3.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Gupta, Gp" uniqKey="Gupta G">GP Gupta</name></author><author><name sortKey="Massague, J" uniqKey="Massague J">J Massague</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Stacker, Sa" uniqKey="Stacker S">SA Stacker</name></author><author><name sortKey="Achen, Mg" uniqKey="Achen M">MG Achen</name></author><author><name sortKey="Jussila, L" uniqKey="Jussila L">L Jussila</name></author><author><name sortKey="Baldwin, Me" uniqKey="Baldwin M">ME Baldwin</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author><author><name sortKey="Tammela, T" uniqKey="Tammela T">T Tammela</name></author><author><name sortKey="Petrova, Tv" uniqKey="Petrova T">TV Petrova</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Joyce, Ja" uniqKey="Joyce J">JA Joyce</name></author><author><name sortKey="Pollard, Jw" uniqKey="Pollard J">JW Pollard</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Tammela, T" uniqKey="Tammela T">T Tammela</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Achen, Mg" uniqKey="Achen M">MG Achen</name></author><author><name sortKey="Mccoll, Bk" uniqKey="Mccoll B">BK McColl</name></author><author><name sortKey="Stacker, Sa" uniqKey="Stacker S">SA Stacker</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Adams, Rh" uniqKey="Adams R">RH Adams</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zwaans, Bm" uniqKey="Zwaans B">BM Zwaans</name></author><author><name sortKey="Bielenberg, Dr" uniqKey="Bielenberg D">DR Bielenberg</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Skobe, M" uniqKey="Skobe M">M Skobe</name></author><author><name sortKey="Hawighorst, T" uniqKey="Hawighorst T">T Hawighorst</name></author><author><name sortKey="Jackson, Dg" uniqKey="Jackson D">DG Jackson</name></author><author><name sortKey="Prevo, R" uniqKey="Prevo R">R Prevo</name></author><author><name sortKey="Janes, L" uniqKey="Janes L">L Janes</name></author><author><name sortKey="Velasco, P" uniqKey="Velasco P">P Velasco</name></author><author><name sortKey="Riccardi, L" uniqKey="Riccardi L">L Riccardi</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author><author><name sortKey="Claffey, K" uniqKey="Claffey K">K Claffey</name></author><author><name sortKey="Detmar, M" uniqKey="Detmar M">M Detmar</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Stacker, Sa" uniqKey="Stacker S">SA Stacker</name></author><author><name sortKey="Caesar, C" uniqKey="Caesar C">C Caesar</name></author><author><name sortKey="Baldwin, Me" uniqKey="Baldwin M">ME Baldwin</name></author><author><name sortKey="Thornton, Ge" uniqKey="Thornton G">GE Thornton</name></author><author><name sortKey="Williams, Ra" uniqKey="Williams R">RA Williams</name></author><author><name sortKey="Prevo, R" uniqKey="Prevo R">R Prevo</name></author><author><name sortKey="Jackson, Dg" uniqKey="Jackson D">DG Jackson</name></author><author><name sortKey="Nishikawa, S" uniqKey="Nishikawa S">S Nishikawa</name></author><author><name sortKey="Kubo, H" uniqKey="Kubo H">H Kubo</name></author><author><name sortKey="Achen, Mg" uniqKey="Achen M">MG Achen</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Podgrabinska, S" uniqKey="Podgrabinska S">S Podgrabinska</name></author><author><name sortKey="Braun, P" uniqKey="Braun P">P Braun</name></author><author><name sortKey="Velasco, P" uniqKey="Velasco P">P Velasco</name></author><author><name sortKey="Kloos, B" uniqKey="Kloos B">B Kloos</name></author><author><name sortKey="Pepper, Ms" uniqKey="Pepper M">MS Pepper</name></author><author><name sortKey="Skobe, M" uniqKey="Skobe M">M Skobe</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zeng, Y" uniqKey="Zeng Y">Y Zeng</name></author><author><name sortKey="Opeskin, K" uniqKey="Opeskin K">K Opeskin</name></author><author><name sortKey="Goad, J" uniqKey="Goad J">J Goad</name></author><author><name sortKey="Williams, Ed" uniqKey="Williams E">ED Williams</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wissmann, C" uniqKey="Wissmann C">C Wissmann</name></author><author><name sortKey="Detmar, M" uniqKey="Detmar M">M Detmar</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Dumont, Dj" uniqKey="Dumont D">DJ Dumont</name></author><author><name sortKey="Jussila, L" uniqKey="Jussila L">L Jussila</name></author><author><name sortKey="Taipale, J" uniqKey="Taipale J">J Taipale</name></author><author><name sortKey="Lymboussaki, A" uniqKey="Lymboussaki A">A Lymboussaki</name></author><author><name sortKey="Mustonen, T" uniqKey="Mustonen T">T Mustonen</name></author><author><name sortKey="Pajusola, K" uniqKey="Pajusola K">K Pajusola</name></author><author><name sortKey="Breitman, M" uniqKey="Breitman M">M Breitman</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="M Kinen, T" uniqKey="M Kinen T">T Mäkinen</name></author><author><name sortKey="Jussila, L" uniqKey="Jussila L">L Jussila</name></author><author><name sortKey="Veikkola, T" uniqKey="Veikkola T">T Veikkola</name></author><author><name sortKey="Karpanen, T" uniqKey="Karpanen T">T Karpanen</name></author><author><name sortKey="Kettunen, Mi" uniqKey="Kettunen M">MI Kettunen</name></author><author><name sortKey="Pulkkanen, Kj" uniqKey="Pulkkanen K">KJ Pulkkanen</name></author><author><name sortKey="Kauppinen, R" uniqKey="Kauppinen R">R Kauppinen</name></author><author><name sortKey="Jackson, Dg" uniqKey="Jackson D">DG Jackson</name></author><author><name sortKey="Kubo, H" uniqKey="Kubo H">H Kubo</name></author><author><name sortKey="Nishikawa, S" uniqKey="Nishikawa S">S Nishikawa</name></author><author><name sortKey="Yl Herttuala, S" uniqKey="Yl Herttuala S">S Ylä-Herttuala</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Kriehuber, E" uniqKey="Kriehuber E">E Kriehuber</name></author><author><name sortKey="Breiteneder Geleff, S" uniqKey="Breiteneder Geleff S">S Breiteneder-Geleff</name></author><author><name sortKey="Groeger, M" uniqKey="Groeger M">M Groeger</name></author><author><name sortKey="Soleiman, A" uniqKey="Soleiman A">A Soleiman</name></author><author><name sortKey="Schoppmann, Sf" uniqKey="Schoppmann S">SF Schoppmann</name></author><author><name sortKey="Stingl, G" uniqKey="Stingl G">G Stingl</name></author><author><name sortKey="Kerjaschki, D" uniqKey="Kerjaschki D">D Kerjaschki</name></author><author><name sortKey="Maurer, D" uniqKey="Maurer D">D Maurer</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Saaristo, A" uniqKey="Saaristo A">A Saaristo</name></author><author><name sortKey="Veikkola, T" uniqKey="Veikkola T">T Veikkola</name></author><author><name sortKey="Enholm, B" uniqKey="Enholm B">B Enholm</name></author><author><name sortKey="Hytonen, M" uniqKey="Hytonen M">M Hytönen</name></author><author><name sortKey="Arola, J" uniqKey="Arola J">J Arola</name></author><author><name sortKey="Pajusola, K" uniqKey="Pajusola K">K Pajusola</name></author><author><name sortKey="Turunen, P" uniqKey="Turunen P">P Turunen</name></author><author><name sortKey="Jeltsch, M" uniqKey="Jeltsch M">M Jeltsch</name></author><author><name sortKey="Karkkainen, Mj" uniqKey="Karkkainen M">MJ Karkkainen</name></author><author><name sortKey="Kerjaschki, D" uniqKey="Kerjaschki D">D Kerjaschki</name></author><author><name sortKey="Bueler, H" uniqKey="Bueler H">H Bueler</name></author><author><name sortKey="Yl Herttuala, S" uniqKey="Yl Herttuala S">S Ylä-Herttuala</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Goldman, J" uniqKey="Goldman J">J Goldman</name></author><author><name sortKey="Rutkowski, Jm" uniqKey="Rutkowski J">JM Rutkowski</name></author><author><name sortKey="Shields, Jd" uniqKey="Shields J">JD Shields</name></author><author><name sortKey="Pasquier, Mc" uniqKey="Pasquier M">MC Pasquier</name></author><author><name sortKey="Cui, Y" uniqKey="Cui Y">Y Cui</name></author><author><name sortKey="Schmokel, Hg" uniqKey="Schmokel H">HG Schmokel</name></author><author><name sortKey="Willey, S" uniqKey="Willey S">S Willey</name></author><author><name sortKey="Hicklin, Dj" uniqKey="Hicklin D">DJ Hicklin</name></author><author><name sortKey="Pytowski, B" uniqKey="Pytowski B">B Pytowski</name></author><author><name sortKey="Swartz, Ma" uniqKey="Swartz M">MA Swartz</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="He, Y" uniqKey="He Y">Y He</name></author><author><name sortKey="Kozaki, K" uniqKey="Kozaki K">K Kozaki</name></author><author><name sortKey="Karpanen, T" uniqKey="Karpanen T">T Karpanen</name></author><author><name sortKey="Koshikawa, K" uniqKey="Koshikawa K">K Koshikawa</name></author><author><name sortKey="Yla Herttuala, S" uniqKey="Yla Herttuala S">S Yla-Herttuala</name></author><author><name sortKey="Takahashi, T" uniqKey="Takahashi T">T Takahashi</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Roberts, N" uniqKey="Roberts N">N Roberts</name></author><author><name sortKey="Kloos, B" uniqKey="Kloos B">B Kloos</name></author><author><name sortKey="Cassella, M" uniqKey="Cassella M">M Cassella</name></author><author><name sortKey="Podgrabinska, S" uniqKey="Podgrabinska S">S Podgrabinska</name></author><author><name sortKey="Persaud, K" uniqKey="Persaud K">K Persaud</name></author><author><name sortKey="Wu, Y" uniqKey="Wu Y">Y Wu</name></author><author><name sortKey="Pytowski, B" uniqKey="Pytowski B">B Pytowski</name></author><author><name sortKey="Skobe, M" uniqKey="Skobe M">M Skobe</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Burton, Jb" uniqKey="Burton J">JB Burton</name></author><author><name sortKey="Priceman, Sj" uniqKey="Priceman S">SJ Priceman</name></author><author><name sortKey="Sung, Jl" uniqKey="Sung J">JL Sung</name></author><author><name sortKey="Brakenhielm, E" uniqKey="Brakenhielm E">E Brakenhielm</name></author><author><name sortKey="An, Ds" uniqKey="An D">DS An</name></author><author><name sortKey="Pytowski, B" uniqKey="Pytowski B">B Pytowski</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author><author><name sortKey="Wu, L" uniqKey="Wu L">L Wu</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Matsui, J" uniqKey="Matsui J">J Matsui</name></author><author><name sortKey="Funahashi, Y" uniqKey="Funahashi Y">Y Funahashi</name></author><author><name sortKey="Uenaka, T" uniqKey="Uenaka T">T Uenaka</name></author><author><name sortKey="Watanabe, T" uniqKey="Watanabe T">T Watanabe</name></author><author><name sortKey="Tsuruoka, A" uniqKey="Tsuruoka A">A Tsuruoka</name></author><author><name sortKey="Asada, M" uniqKey="Asada M">M Asada</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Heckman, Ca" uniqKey="Heckman C">CA Heckman</name></author><author><name sortKey="Holopainen, T" uniqKey="Holopainen T">T Holopainen</name></author><author><name sortKey="Wirzenius, M" uniqKey="Wirzenius M">M Wirzenius</name></author><author><name sortKey="Keskitalo, S" uniqKey="Keskitalo S">S Keskitalo</name></author><author><name sortKey="Jeltsch, M" uniqKey="Jeltsch M">M Jeltsch</name></author><author><name sortKey="Yla Herttuala, S" uniqKey="Yla Herttuala S">S Yla-Herttuala</name></author><author><name sortKey="Wedge, Sr" uniqKey="Wedge S">SR Wedge</name></author><author><name sortKey="Jurgensmeier, Jm" uniqKey="Jurgensmeier J">JM Jurgensmeier</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Schomber, T" uniqKey="Schomber T">T Schomber</name></author><author><name sortKey="Zumsteg, A" uniqKey="Zumsteg A">A Zumsteg</name></author><author><name sortKey="Strittmatter, K" uniqKey="Strittmatter K">K Strittmatter</name></author><author><name sortKey="Crnic, I" uniqKey="Crnic I">I Crnic</name></author><author><name sortKey="Antoniadis, H" uniqKey="Antoniadis H">H Antoniadis</name></author><author><name sortKey="Littlewood Evans, A" uniqKey="Littlewood Evans A">A Littlewood-Evans</name></author><author><name sortKey="Wood, J" uniqKey="Wood J">J Wood</name></author><author><name sortKey="Christofori, G" uniqKey="Christofori G">G Christofori</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Faivre, S" uniqKey="Faivre S">S Faivre</name></author><author><name sortKey="Demetri, G" uniqKey="Demetri G">G Demetri</name></author><author><name sortKey="Sargent, W" uniqKey="Sargent W">W Sargent</name></author><author><name sortKey="Raymond, E" uniqKey="Raymond E">E Raymond</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Jenkins, De" uniqKey="Jenkins D">DE Jenkins</name></author><author><name sortKey="Hornig, Ys" uniqKey="Hornig Y">YS Hornig</name></author><author><name sortKey="Oei, Y" uniqKey="Oei Y">Y Oei</name></author><author><name sortKey="Dusich, J" uniqKey="Dusich J">J Dusich</name></author><author><name sortKey="Purchio, T" uniqKey="Purchio T">T Purchio</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Fukai, J" uniqKey="Fukai J">J Fukai</name></author><author><name sortKey="Nishio, K" uniqKey="Nishio K">K Nishio</name></author><author><name sortKey="Itakura, T" uniqKey="Itakura T">T Itakura</name></author><author><name sortKey="Koizumi, F" uniqKey="Koizumi F">F Koizumi</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Dixelius, J" uniqKey="Dixelius J">J Dixelius</name></author><author><name sortKey="Makinen, T" uniqKey="Makinen T">T Makinen</name></author><author><name sortKey="Wirzenius, M" uniqKey="Wirzenius M">M Wirzenius</name></author><author><name sortKey="Karkkainen, Mj" uniqKey="Karkkainen M">MJ Karkkainen</name></author><author><name sortKey="Wernstedt, C" uniqKey="Wernstedt C">C Wernstedt</name></author><author><name sortKey="Alitalo, K" uniqKey="Alitalo K">K Alitalo</name></author><author><name sortKey="Claesson Welsh, L" uniqKey="Claesson Welsh L">L Claesson-Welsh</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Alam, A" uniqKey="Alam A">A Alam</name></author><author><name sortKey="Herault, Jp" uniqKey="Herault J">JP Herault</name></author><author><name sortKey="Barron, P" uniqKey="Barron P">P Barron</name></author><author><name sortKey="Favier, B" uniqKey="Favier B">B Favier</name></author><author><name sortKey="Fons, P" uniqKey="Fons P">P Fons</name></author><author><name sortKey="Delesque Touchard, N" uniqKey="Delesque Touchard N">N Delesque-Touchard</name></author><author><name sortKey="Senegas, I" uniqKey="Senegas I">I Senegas</name></author><author><name sortKey="Laboudie, P" uniqKey="Laboudie P">P Laboudie</name></author><author><name sortKey="Bonnin, J" uniqKey="Bonnin J">J Bonnin</name></author><author><name sortKey="Cassan, C" uniqKey="Cassan C">C Cassan</name></author><author><name sortKey="Savi, P" uniqKey="Savi P">P Savi</name></author><author><name sortKey="Ruggeri, B" uniqKey="Ruggeri B">B Ruggeri</name></author><author><name sortKey="Carmeliet, P" uniqKey="Carmeliet P">P Carmeliet</name></author><author><name sortKey="Bono, F" uniqKey="Bono F">F Bono</name></author><author><name sortKey="Herbert, Jm" uniqKey="Herbert J">JM Herbert</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Morelli, Mp" uniqKey="Morelli M">MP Morelli</name></author><author><name sortKey="Brown, Am" uniqKey="Brown A">AM Brown</name></author><author><name sortKey="Pitts, Tm" uniqKey="Pitts T">TM Pitts</name></author><author><name sortKey="Tentler, Jj" uniqKey="Tentler J">JJ Tentler</name></author><author><name sortKey="Ciardiello, F" uniqKey="Ciardiello F">F Ciardiello</name></author><author><name sortKey="Ryan, A" uniqKey="Ryan A">A Ryan</name></author><author><name sortKey="Jurgensmeier, Jm" uniqKey="Jurgensmeier J">JM Jurgensmeier</name></author><author><name sortKey="Eckhardt, Sg" uniqKey="Eckhardt S">SG Eckhardt</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Blansfield, Ja" uniqKey="Blansfield J">JA Blansfield</name></author><author><name sortKey="Caragacianu, D" uniqKey="Caragacianu D">D Caragacianu</name></author><author><name sortKey="Alexander, Hr" uniqKey="Alexander H">HR Alexander</name></author><author><name sortKey="Tangrea, Ma" uniqKey="Tangrea M">MA Tangrea</name></author><author><name sortKey="Morita, Sy" uniqKey="Morita S">SY Morita</name></author><author><name sortKey="Lorang, D" uniqKey="Lorang D">D Lorang</name></author><author><name sortKey="Schafer, P" uniqKey="Schafer P">P Schafer</name></author><author><name sortKey="Muller, G" uniqKey="Muller G">G Muller</name></author><author><name sortKey="Stirling, D" uniqKey="Stirling D">D Stirling</name></author><author><name sortKey="Royal, Re" uniqKey="Royal R">RE Royal</name></author><author><name sortKey="Libutti, Sk" uniqKey="Libutti S">SK Libutti</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Zhang, L" uniqKey="Zhang L">L Zhang</name></author><author><name sortKey="Smith, Km" uniqKey="Smith K">KM Smith</name></author><author><name sortKey="Chong, Al" uniqKey="Chong A">AL Chong</name></author><author><name sortKey="Stempak, D" uniqKey="Stempak D">D Stempak</name></author><author><name sortKey="Yeger, H" uniqKey="Yeger H">H Yeger</name></author><author><name sortKey="Marrano, P" uniqKey="Marrano P">P Marrano</name></author><author><name sortKey="Thorner, Ps" uniqKey="Thorner P">PS Thorner</name></author><author><name sortKey="Irwin, Ms" uniqKey="Irwin M">MS Irwin</name></author><author><name sortKey="Kaplan, Dr" uniqKey="Kaplan D">DR Kaplan</name></author><author><name sortKey="Baruchel, S" uniqKey="Baruchel S">S Baruchel</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ebos, Jm" uniqKey="Ebos J">JM Ebos</name></author><author><name sortKey="Lee, Cr" uniqKey="Lee C">CR Lee</name></author><author><name sortKey="Cruz Munoz, W" uniqKey="Cruz Munoz W">W Cruz-Munoz</name></author><author><name sortKey="Bjarnason, Ga" uniqKey="Bjarnason G">GA Bjarnason</name></author><author><name sortKey="Christensen, Jg" uniqKey="Christensen J">JG Christensen</name></author><author><name sortKey="Kerbel, Rs" uniqKey="Kerbel R">RS Kerbel</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Paez Ribes, M" uniqKey="Paez Ribes M">M Paez-Ribes</name></author><author><name sortKey="Allen, E" uniqKey="Allen E">E Allen</name></author><author><name sortKey="Hudock, J" uniqKey="Hudock J">J Hudock</name></author><author><name sortKey="Takeda, T" uniqKey="Takeda T">T Takeda</name></author><author><name sortKey="Okuyama, H" uniqKey="Okuyama H">H Okuyama</name></author><author><name sortKey="Vinals, F" uniqKey="Vinals F">F Vinals</name></author><author><name sortKey="Inoue, M" uniqKey="Inoue M">M Inoue</name></author><author><name sortKey="Bergers, G" uniqKey="Bergers G">G Bergers</name></author><author><name sortKey="Hanahan, D" uniqKey="Hanahan D">D Hanahan</name></author><author><name sortKey="Casanovas, O" uniqKey="Casanovas O">O Casanovas</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Breast Cancer Res</journal-id><journal-title-group><journal-title>Breast Cancer Research : BCR</journal-title></journal-title-group><issn pub-type="ppub">1465-5411</issn><issn pub-type="epub">1465-542X</issn><publisher><publisher-name>BioMed Central</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">21693010</article-id><article-id pub-id-type="pmc">3218955</article-id><article-id pub-id-type="publisher-id">bcr2903</article-id><article-id pub-id-type="doi">10.1186/bcr2903</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Sunitinib inhibits lymphatic endothelial cell functions and lymph node metastasis in a breast cancer model through inhibition of vascular endothelial growth factor receptor 3</article-title></title-group><contrib-group><contrib contrib-type="author" id="A1"><name><surname>Kodera</surname><given-names>Yasuo</given-names></name><xref ref-type="aff" rid="I1">1</xref><xref ref-type="aff" rid="I2">2</xref><email>ykoyko2003jp@yahoo.co.jp</email></contrib><contrib contrib-type="author" id="A2"><name><surname>Katanasaka</surname><given-names>Yasufumi</given-names></name><xref ref-type="aff" rid="I3">3</xref><email>katana@u-shizuoka-ken.ac.jp</email></contrib><contrib contrib-type="author" id="A3"><name><surname>Kitamura</surname><given-names>Yuka</given-names></name><xref ref-type="aff" rid="I1">1</xref><email>yukitamu@ncc.go.jp</email></contrib><contrib contrib-type="author" id="A4"><name><surname>Tsuda</surname><given-names>Hitoshi</given-names></name><xref ref-type="aff" rid="I4">4</xref><email>hstsuda@ncc.go.jp</email></contrib><contrib contrib-type="author" id="A5"><name><surname>Nishio</surname><given-names>Kazuto</given-names></name><xref ref-type="aff" rid="I2">2</xref><email>knishio@med.kindai.ac.jp</email></contrib><contrib contrib-type="author" id="A6"><name><surname>Tamura</surname><given-names>Tomohide</given-names></name><xref ref-type="aff" rid="I5">5</xref><email>ttamura@ncc.go.jp</email></contrib><contrib contrib-type="author" corresp="yes" id="A7"><name><surname>Koizumi</surname><given-names>Fumiaki</given-names></name><xref ref-type="aff" rid="I1">1</xref><email>fkoizumi@ncc.go.jp</email></contrib></contrib-group><aff id="I1"><label>1</label>Shien-Lab, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</aff><aff id="I2"><label>2</label>Department of Genome Biology, Kinki University Faculty of Medicine, 377-2 Ohno-higashi, Osaka-Sayama, Osaka 589-8511, Japan</aff><aff id="I3"><label>3</label>Division of Molecular Medicine, Graduate School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan</aff><aff id="I4"><label>4</label>Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</aff><aff id="I5"><label>5</label>Department of Thoracic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104-0045, Japan</aff><pub-date pub-type="ppub"><year>2011</year></pub-date><pub-date pub-type="epub"><day>21</day><month>6</month><year>2011</year></pub-date><volume>13</volume><issue>3</issue><fpage>R66</fpage><lpage>R66</lpage><history><date date-type="received"><day>9</day><month>9</month><year>2010</year></date><date date-type="rev-recd"><day>28</day><month>2</month><year>2011</year></date><date date-type="accepted"><day>21</day><month>6</month><year>2011</year></date></history><permissions><copyright-statement>Copyright ©2011 Kodera et al.; licensee BioMed Central Ltd.</copyright-statement><copyright-year>2011</copyright-year><copyright-holder>Kodera et al.; licensee BioMed Central Ltd.</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0"><license-p>This is an open access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0">http://creativecommons.org/licenses/by/2.0</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><self-uri xlink:href="http://breast-cancer-research.com/content/13/3/R66"></self-uri><abstract><sec><title>Introduction</title><p>Metastasis is a common event and the main cause of death in cancer patients. Lymphangiogenesis refers to the formation of new lymphatic vessels and is thought to be involved in the development of metastasis. Sunitinib is a multi-kinase inhibitor that blocks receptor tyrosine kinase activity, including that of vascular endothelial growth factor receptors (VEGFRs). Although sunitinib is a clinically available angiogenesis inhibitor, its effects on lymphangiogenesis and lymph node metastasis remain unclear. The purpose of this study was to investigate the effects of sunitinib on vascular endothelial growth factor receptor 3 (VEGFR-3) and a related event, lymphangiogenesis.</p></sec><sec><title>Methods</title><p>The effects of sunitinib on the degree of phosphorylation of VEGFR-2/3 and other signaling molecules was examined in lymphatic endothelial cells (LECs) treated with the drug; VEGF-induced LEC growth, migration, and tube formation were also examined. For the <italic>in vivo </italic>study, luciferase-expressing breast cancer cells were transplanted into mammary fat pads of mice; the microvessel and lymphatic vessel density was then measured after treatment with sunitinib and anti-VEGFR-2 antibody.</p></sec><sec><title>Results</title><p>First, in human LECs, sunitinib blocked both VEGFR-2 and VEGFR-3 phosphorylation induced by VEGF-C or VEGF-D, and abrogated the activation of the downstream molecules extracellular signal-regulated kinase 1/2 (ERK1/2) and Akt. Furthermore, sunitinib attenuated the cell-proliferation activity induced by VEGF-C/D and prevented VEGF-C-induced migration and tube formation of the LECs; however, anti-VEGFR2 treatment shows only a partial effect on the growth and functions of the LECs. We used a breast cancer cell line expressing luciferase as a metastatic cancer model. Sunitinib treatment (40 mg/kg/day) inhibited the growth of the primary tumor transplanted in the mammary fat pad of the mice and significantly reduced the number of blood and lymphatic vessels in the tumor. Furthermore, the development of axillary lymph node metastasis, detected by bioluminescent imaging, was markedly suppressed. This effect of sunitinib was more potent than that of DC101, an anti-mouse VEGFR-2 antibody.</p></sec><sec><title>Conclusions</title><p>The results suggest that sunitinib might be beneficial for the treatment of breast cancer by suppressing lymphangiogenesis and lymph node metastasis, through inhibition, particularly important, of VEGFR-3.</p></sec></abstract></article-meta></front><body><sec><title>Introduction</title><p>Metastasis is the main cause of therapeutic failure and death in cancer patients [<xref ref-type="bibr" rid="B1">1</xref>]. Tumor cells disseminate to distant organs through lymphatic vessels and blood vessels [<xref ref-type="bibr" rid="B2">2</xref>]. The status of metastasis to the regional lymph nodes is a prognostic factor in patients with malignancies and a determinant of the treatment course of patients [<xref ref-type="bibr" rid="B3">3</xref>]. Lymph nodes have also been proposed to serve as a cancer cell reservoir, providing a supportive environment for further movement of the cancer cells to distal organs [<xref ref-type="bibr" rid="B4">4</xref>,<xref ref-type="bibr" rid="B5">5</xref>]. Previously, this metastatic process was thought to be passively initiated via preexisting lymphatic vasculature; however, recent studies suggest that new lymphatic vessel formation, called lymphangiogenesis, actively contributes to lymphatic metastasis. In a clinical study, lymphatic vessel density in a tumor was correlated with the risk of lymph node metastasis and a poor prognosis [<xref ref-type="bibr" rid="B6">6</xref>]. Therefore, therapies targeting tumor lymphangiogenesis are expected to suppress the risk of development of metastasis and provide clinical benefit in cancer patients.</p><p>The lymphangiogenic process is regulated by numerous molecules, including the vascular endothelial growth factor (VEGF) and VEGF receptor (VEGFR) family. Among them, VEGF-C and VEGF-D are well-studied potent inducers of lymphangiogenesis [<xref ref-type="bibr" rid="B7">7</xref>]. A large number of clinical studies have demonstrated that the expression levels of VEGF-C/VEGF-D are markedly associated with lymphangiogenesis and lymph node metastasis in various types of cancers, including breast, ovarian, lung, and colon cancer [<xref ref-type="bibr" rid="B8">8</xref>]; their forced expression in cancer cells was shown to induce tumor lymphangiogenesis and lymph node metastasis in a preclinical model [<xref ref-type="bibr" rid="B9">9</xref>,<xref ref-type="bibr" rid="B10">10</xref>]. In <italic>in vitro </italic>analyses, VEGF-C and VEGF-D have been shown to induce various cellular functions of the lymphatic endothelial cells (LECs) that constitute lymphatic capillaries. These cellular functions include proliferation, migration, and tube formation, which are important for lymphatic vascular development [<xref ref-type="bibr" rid="B11">11</xref>,<xref ref-type="bibr" rid="B12">12</xref>]. Their receptors, VEGFR-2 and VEGFR-3, are tyrosine kinase receptors, and under VEGFC/D stimulation, undergo autophosphorylation and activate the downstream molecules Akt and extracellular signal-regulated kinase1/2 (ERK1/2) [<xref ref-type="bibr" rid="B13">13</xref>].</p><p>VEGFR-3 is expressed in all endothelial cells and is necessary for the formation of the primary vascular plexus in early development; subsequently, its expression becomes restricted, with the exception of the fenestrated blood vessels, to LECs [<xref ref-type="bibr" rid="B5">5</xref>]. The results of experimental studies indicate that VEGFR-3 signaling plays a key role in the development of the lymphatic vascular network [<xref ref-type="bibr" rid="B14">14</xref>,<xref ref-type="bibr" rid="B15">15</xref>]. VEGFR-2 is a well-known mediator of blood vessel formation and has been shown to be expressed in the LECs and lymphatic endothelium <italic>in vivo </italic>[<xref ref-type="bibr" rid="B16">16</xref>,<xref ref-type="bibr" rid="B17">17</xref>]. Furthermore, VEGFR-2 and VEGFR-3 form homodimer and heterodimer complexes in the LECs and exhibit cooperative and redundant functions in adult lymphangiogenesis [<xref ref-type="bibr" rid="B18">18</xref>].</p><p>Targeting of VEGF and VEGFR signaling in a tumor has been considered a therapeutic strategy. To achieve this, several approaches have been examined, including use of antibodies against VEGF receptors [<xref ref-type="bibr" rid="B19">19</xref>,<xref ref-type="bibr" rid="B20">20</xref>], soluble receptors [<xref ref-type="bibr" rid="B21">21</xref>], and small molecules [<xref ref-type="bibr" rid="B22">22</xref>-<xref ref-type="bibr" rid="B24">24</xref>]. In particular, multitargeting of small molecules has been reported to be highly effective in animal models. Given the complexity and redundancy of the VEGF signaling network, multitargeting may be a better strategy for effective inhibition of lymphangiogenesis.</p><p>Before this approach, angiogenesis inhibitors targeting the VEGF-A and VEGFR-2 signaling pathways were developed [<xref ref-type="bibr" rid="B25">25</xref>]. Sunitinib and bevacizumab are already approved angiogenesis inhibitors available for the treatment of renal cell carcinoma and metastatic gastrointestinal stromal tumors that prove resistant to imatinib. Sunitinib inhibits receptor tyrosine kinase activity, including that of VEGFR, PDGFR, KIT, FLT3, RET, and CSF1R. Although one of the main mechanisms underlying tumor growth inhibition by sunitinib appears to be its antiangiogenic activity exerted via its inhibitory action on VEGFR2 kinase activity in blood endothelial cells, its influence on lymphatic cell functions and tumor lymphangiogenesis remains unclear.</p><p>In this study, we evaluated the effect of sunitinib on lymphangiogenesis and lymph node metastasis. For this purpose, we used lymphatic dermal endothelial cells for <italic>in vitro </italic>analyses with the endogenous ligands VEGF-C and VEGF-D. To examine lymphangiogenesis <italic>in vivo</italic>, MDA-MB-231luc-D3H2LN (MDA-MB-231LN), a daughter cell line of the metastatic breast cancer MDA-MB-231, was used along with the bioluminescent imaging technology. We found that sunitinib inhibited VEGFR-2 and VEGFR-3 activity simultaneously, thereby inhibiting the cellular functions of the LECs, including proliferation, migration, and tube formation. In addition, it attenuated tumor lymphangiogenesis and lymph node metastasis in a mouse mammary fat pad (m.f.p.) model. This is the first article reporting that sunitinib, which is a clinically available angiogenesis inhibitor, blocks VEGFR-3 signaling in LECs to suppress lymphangiogenesis.</p></sec><sec sec-type="materials|methods"><title>Materials and methods</title><sec><title>Reagents and cells</title><p>Sunitinib (Symansis, Washdyke, New Zealand, and Pfizer, New York, NY) was resuspended in dimethyl sulfoxide (DMSO) and diluted in cell medium or PBS for the <italic>in vitro </italic>and <italic>in vivo </italic>assays. Recombinant human VEGF-C and VEGF-D were dissolved in sterile PBS containing 0.1% bovine serum albumin and stored at -80°C. The following antibodies were used: mouse monoclonal VEGFR-3 and phosphotyrosine (Upstate Biotechnology, Inc., Lake Placid, NY), ERK1/2, phospho-ERK1/2, Akt, phospho-Akt, c-Raf, phospho-c-Raf, MEK, phospho-MEK (Cell Signaling Technology, Beverly, MA), ras (abcam), CD31 (BD Pharmingen, San Jose, CA), lymphatic vessel endothelial hyaluronan receptor LYVE-1 (Upstate Biotechnology), and neutralizing VEGFR-2 antibody (R&D Systems, Minneapolis, MN). LECs were purchased from Lonza (Gaithersburg, MD) and maintained in EGM-2 according to the supplier's instructions. Cancer cell lines were purchased from the American Type Culture Collection (Manassas, VA). The MDA-MB-231luc-D3H2LN (MDA-MB-231LN) cell line was obtained from Caliper (Hopkinton, MA). An MDA-MB-231LN cell line stably expressing luciferase protein was established and maintained as described in [<xref ref-type="bibr" rid="B26">26</xref>].</p></sec><sec><title>Immunoprecipitation and Western-blot analysis</title><p>Cells were cultured overnight in a serum-free medium. The medium was replaced with a medium containing DMSO or sunitinib for 2 hours, and the cells were then stimulated with VEGF-C/D for 10 minutes. Cells were rinsed with cold PBS and lysed with RIPA buffer (25 m<italic>M </italic>Tris HCl (pH 7.6), 150 m<italic>M </italic>NaCl, 1% NP-40, 1% sodium deoxycholate, 0.1% SDS, phosphatase inhibitor cocktail (Sigma, Saint Louis, MO), and complete protease inhibitor (Roche, Indianapolis, IN)). For detection of phosphorylated VEGFR-3, cell lysates were immunoprecipitated with anti-VEGFR-3 and then pulled down with protein G (Santa Cruz Biotechnology, Santa Cruz, CA). Samples were dissolved in SDS sample buffer and electrophoresed on 10% SDS-PAGE gel before being transferred to a PVDF membrane. To detect downstream signaling, confluent LEC cultures were stimulated and harvested as described. The same amounts of lysates were separated by 12% SDS-PAGE and then blotted onto a PVDF membrane. Phosphorylated proteins were detected with the respective antibodies, as described earlier. After detection, the antibodies were removed with stripping buffer (Pierce, Rockford, IL), and the membranes were reblotted with anti-ERK1/2 and anti-Akt.</p></sec><sec><title>LEC proliferation assay</title><p>To evaluate the effect of inhibitors and antibodies on LEC growth, we used the MTS assay, as previously described [<xref ref-type="bibr" rid="B27">27</xref>]. In brief, a 200-μl volume of an LEC cell suspension was seeded into each well of a 96-well plate (3,000 cells/well). The cells were cultured overnight before the medium was replaced with a serum-free medium containing growth factors and inhibitors. The concentrations of VEGF-C and VEGF-D were 500 ng/ml. The cells were exposed to each drug at various concentrations and cultured at 37°C in a humidified atmosphere for 72 hours. After the culture period, 40 μl of MTS solution was added to each well, and the plates were incubated for a further 4 hours at 37°C. The growth-inhibitory effects of each drug were assessed spectrophotometrically (Spectra Max 190; Molecular Devices Corporation, Sunnyvale, CA). The results were evaluated with analysis of variance (ANOVA).</p></sec><sec><title>LEC migration assay</title><p>LECs were suspended in a serum-free medium and seeded in the top chamber of a cell-culture insert (BD Biosciences, Bedford, MA) with DMSO or sunitinib. The inserts were placed in 24-well plates and incubated with medium containing VEGF-C for 24 hours. The migrated cells were fixed with glutaraldehyde and stained with crystal violet. The cell numbers were counted under a microscope, and relative migration was evaluated by dividing the number of sunitinib-treated cells by the number of control cells.</p></sec><sec><title>Tube-formation assay</title><p>LECs were trypsinized and resuspended in a serum-free medium and then seeded on culture plates (2 × 10<sup>4 </sup>cells/well). After overnight culture, collagen I gel (3 mg/ml) was layered on the plated cells containing DMSO, sunitinib, or anti-VEGFR2. Cells were incubated for 16 hours at 37°C, in a 5% CO<sub>2 </sub>atmosphere.</p></sec><sec><title>Quantification of the secreted protein (ELISA)</title><p>Cancer cells were cultured in a 12-well plate (1.2 × 10<sup>5</sup>) with basal medium containing 0.1% bovine serum albumin for 24 hours. The amount of secreted VEGF-A, VEGF-C, and VEGF-D in the cultured medium was quantified by using ELISA detection kits (R&D Systems).</p></sec><sec><title>The m.f.p. model</title><p>MDA-MB-231LN was trypsinized and resuspended in a 50% DPBS/50% matrigel. The cells were implanted into the left abdominal m.f.p. site of 6- to 7-week-old SCID mice. Five days after the transplantation, the mice were randomized and divided into the control and treatment groups. Depending on the group to which they belonged, the mice were orally administered either vehicle or sunitinib once a day for 2 weeks. Tumor volumes were measured with calipers every 3 or 4 days. After 2 weeks, the lymph node metastasis status was evaluated. All animal experiments were conducted with the approval of the Committee for Ethics in Animal Experimentation, and in accordance with the Guidelines for Animal Experiments of National Cancer Center.</p></sec><sec><title>Immunohistochemical analysis of angiogenesis and lymphangiogenesis</title><p>After treatment, the tumors were excised and embedded in OCT compound. Six-micrometer-thick frozen sections were stained with antibody to CD31 (rat monoclonal antibody; BD Pharmingen) for blood vessels and antibody to LYVE-1 (rabbit polyclonal antibody; Upstate Biotechnology) for lymphatic vessels. Each type of vessel was visualized with EnVision Detection System (DAKO, Glostrup, Denmark) and counted as the number of structures per square millimeter. Three sections from five individual mice were evaluated and then statistically analyzed by using the Dunnett method.</p></sec><sec><title>Evaluation of lymph node metastasis</title><p>Metastasis in the axillary lymph nodes was detected by using the IVIS Imaging System (Xenogen, Alameda, CA). At 10 to 15 minutes after luciferin injection, the mice were placed in the IVIS Imaging System and imaged in the ventral view. To confirm the presence of metastatic cancer cells, the lymph nodes and lungs were excised from the mice at necropsy and imaged <italic>ex vivo</italic>. Data were evaluated with the Dunnett multiple comparisons.</p></sec><sec><title>Statistics</title><p>All data are presented as mean ± standard deviation. Results were considered statistically significant at <italic>P </italic>< 0.05.</p></sec></sec><sec><title>Results</title><sec><title>Sunitinib inhibited VEGFR-2 and VEGFR-3 signaling</title><p>To investigate the mechanism by which sunitinib inhibited lymphangiogenesis, we first used lymphatic vascular endothelial cells. Both VEGFR-2 and VEGFR-3 are expressed in LECs and are significantly phosphorylated by their natural ligands, VEGF-C and VEGF-D (Figure <xref ref-type="fig" rid="F1">1a, b</xref>). The receptor-activation potential of VEGF-C is higher as compared with that of VEGF-D. Sunitinib treatment suppressed these phosphorylations in a dose-dependent manner (IC<sub>50 </sub>= 48 n<italic>M</italic>). Sunitinib at similar concentrations has also been reported to inhibit VEGFR-3 in a cell-free kinase assay [<xref ref-type="bibr" rid="B25">25</xref>]. Taken together, sunitinib is actually an inhibitor of both VEGFR-2 and VEGFR-3 in the LECs. Phosphorylated VEGFRs are considered to mediate cellular functions by activating various types of signaling pathways. ERK1/2 and MEK, members of the mitogen-activated protein kinase family, are downstream molecules of VEGFR and play critical roles in cell growth. Protein kinase B (Akt) also mediates VEGFR signaling via phosphatidylinositol 3-kinase and regulates cell survival and proliferation. Even though ERK1/2, MEK, and Akt were significantly activated by VEGF-C/VEGF-D, sunitinib inhibited their phosphorylations (Figure <xref ref-type="fig" rid="F1">1c, d</xref>; Additional file <xref ref-type="supplementary-material" rid="S1">1</xref> and <xref ref-type="supplementary-material" rid="S2">2</xref>). Because the expression levels of c-Raf and ras and the phosphorylation of c-Raf were not significantly affected by sunitinib, other Rafs or mediators could be involved in this pathway (see Additional data file <xref ref-type="supplementary-material" rid="S1">1</xref>).</p><fig id="F1" position="float"><label>Figure 1</label><caption><p><bold>Sunitinib blocked activation of VEGFR-2 and VEGFR-3 and their downstream molecules in human dermal LECs</bold>. LECs were cultured to confluence, and the medium was replaced with a serum-free medium. After overnight incubation, the cells were pretreated with sunitinib, anti-VEGFR2 antibody, or DMSO (controls), before being stimulated with 200 ng/ml VEGF-C <bold>(a) </bold>or VEGF-D <bold>(b)</bold>. Lysates were immunoprecipitated with VEGFR-3-specific antibody for phospho-VEGFR-3 detection <bold>(c, d)</bold>. Other phosphoproteins were detected with their respective specific antibodies. All samples were separated by 4% to 20% gradient SDS-PAGE gel. The proteins were blotted onto a PVDF membrane and detected by Western blotting. Tyrosine phosphorylation of VEGFR-2 and VEGFR-3 was noted in the cells treated with VEGF-C or VEGF-D. Sunitinib blocked phosphorylation of both VEGFR-3 and VEGFR-2, whereas anti-VEGFR-2 antibody inhibited phosphorylation of only VEGFR-2. Increased phosphorylation of ERK1/2 and Akt was observed in the LECs stimulated with the VEGFs; however, this was attenuated in the cells treated with sunitinib. DMSO, dimethyl sulfoxide; LEC, lymphatic endothelial cell; MW, molecular weight marker; VEGF, vascular endothelial growth factor; VEGFR, vascular endothelial growth factor receptor.</p></caption><graphic xlink:href="bcr2903-1"></graphic></fig><p>To examine the contribution of VEGFR-2 in the stimulation of the VEGFs, we used an anti-VEGFR2 antibody that specifically inhibits VEGFR-2 phosphorylation (IC<sub>50 </sub>= 1.6 μg/ml) (see Additional data file <xref ref-type="supplementary-material" rid="S1">1</xref>, Figure S1C). When we treated the LECs with anti-VEGFR-2 antibody at 2 μg/ml, VEGFR-2 phosphorylation was reduced to almost the same level as that observed with sunitinib treatment at 100 n<italic>M </italic>(Figure <xref ref-type="fig" rid="F1">1</xref>). Interestingly, however, treatment with this antibody was not sufficient to abolish downstream signaling, although the downstream signaling molecules were strongly suppressed by sunitinib.</p><p>Sunitinib inhibited lymphatic endothelial cell growth and cell functions. To analyze the cellular functions, we first performed a growth-inhibition assay. Sunitinib inhibited the growth of LECs induced by VEGF-C and VEGF-D stimulation in a dose-dependent manner (Figure <xref ref-type="fig" rid="F2">2</xref>). At 100 n<italic>M </italic>of sunitinib, the growth of the LECs was completely inhibited. Conversely, anti-VEGFR-2 antibody (2 μg/ml) inhibited the cellular growth only partially. Migration assay and tube-formation assay were then performed. Transwell migration and capillary network formation of LECs were induced by VEGF-C, and sunitinib inhibited both functions at a lower concentration (10 n<italic>M</italic>) than that required for growth inhibition (Figure <xref ref-type="fig" rid="F3">3a</xref>). However, the inhibitory effects of anti-VEGFR-2 antibody treatment (2 μg/ml) on both migration and tube formation were weaker than those of sunitinib.</p><fig id="F2" position="float"><label>Figure 2</label><caption><p><bold>Sunitinib inhibited VEGF-induced proliferation of LECs</bold>. LECs were incubated in serum-free conditions in the absence or presence of 500 ng/ml of VEGF-C (left) or VEGF-D (right), and DMSO or 10 to 300 n<italic>M </italic>sunitinib. The cellular proliferation was quantified by MTS assay after 7 days of treatment. Columns indicate the values in six replicates normalized to the nontreated controls; bars, SD. *<italic>P </italic>< 0.05 compared with control. DMSO, dimethyl sulfoxide; LEC, lymphatic endothelial cell; VEGF, vascular endothelial growth factor; VEGFR, vascular endothelial growth factor receptor.</p></caption><graphic xlink:href="bcr2903-2"></graphic></fig><fig id="F3" position="float"><label>Figure 3</label><caption><p><bold>Sunitinib inhibited VEGF-C-induced functions of LECs</bold>. <bold>(a) </bold>Quantification of LEC migration induced by VEGF-C in cells treated with DMSO or 10 nmol/ml of sunitinib. Relative migration indicates the number of migrated cells normalized to the number of control cells. Columns indicate the values from four experiments; bars, SD. *<italic>P </italic>< 0.05 as compared with control. Sunitinib suppressed VEGF-C-induced LEC migration. <bold>(b) </bold>Photographs of VEGF-C-induced tube formation in cells treated with sunitinib or DMSO (control). VEGF-C promoted cord formation after overlay of type I collagen, which was suppressed by sunitinib treatment, but not by anti-VEGFR2 antibody. The black line represents 200 μm. <bold>(c) </bold>Quantification of tube formation. Columns indicate the values from the data of four fields; bars, SD. Sunitinib inhibited VEGF-C-induced tube formation. *<italic>P </italic>< 0.05 as compared with control. DMSO, dimethyl sulfoxide; LEC, lymphatic endothelial cell; Suni, sunitinib; VEGF, vascular endothelial growth factor; VEGFR, vascular endothelial growth factor receptor.</p></caption><graphic xlink:href="bcr2903-3"></graphic></fig></sec><sec><title>Sunitinib inhibited tumor growth in the m.f.p. model</title><p>To examine the effect of sunitinib on lymphangiogenesis and metastasis, we used the mammary fat pad model with a highly metastatic breast cancer cell line MDA-MB-231LN. MDA-MB-231LN, which is engineered by transfection of the firefly luciferase gene into the MDA-MB-231 cell line, is a well-characterized model [<xref ref-type="bibr" rid="B26">26</xref>]. Before the animal experiments, we evaluated the expression of VEGFs in various types of metastatic cancer cell lines, including breast (MDA-MB-231, MDA-MB-468, MDA-MB-231LN), lung (A549, H226), and colon (HCT-116, SW480) cancer (Figure <xref ref-type="fig" rid="F4">4a</xref>). MDA-MB-231 and MDA-MB-231LN produce large amounts of VEGF-C and VEGF-A. In some cell lines, the expression of VEGF-A and VEGF-C was upregulated under hypoxic conditions. We also tried to detect VEGF-D expression; however, the amount of VEGF-D was below the limit of detection under both hypoxic and normoxic conditions.</p><fig id="F4" position="float"><label>Figure 4</label><caption><p><bold>Expression of VEGF-C in various cancer cell lines; sunitinib inhibited MDA-MB-231LN tumor growth</bold>. <bold>(a) </bold>VEGF expression levels were quantified in metastatic cancer cell lines under normoxic and hypoxic conditions. All cells were cultured overnight under normoxic or hypoxic (5% O<sub>2</sub>) conditions; subsequently, the amounts of VEGFs secreted in the conditioned medium were quantified with enzyme-linked immunosorbent assay <bold>(a)</bold>. Columns indicate the values of four replicates; bars, SD. <bold>(b) </bold>Effects of sunitinib and of the anti-VEGFR-2 antibody, DC101, on the primary tumor growth. MDA-MB-231LN cells were transplanted into the m.f.p. of female mice, and the treatment was initiated on day 5 after the inoculation. Sunitinib was administered orally at 40 mg/kg once a day, and DC101 at 800 μg/mouse i.p. every 3 days for 2 weeks. Tumor volume was measured on the indicated days. Points indicate tumor volume; bars, SEM. *<italic>P </italic>< 0.05 as compared with control. m.f.p., mammary fat pad; N.D., not detected; VEGF, vascular endothelial growth factor; VEGFR, vascular endothelial growth factor receptor.</p></caption><graphic xlink:href="bcr2903-4"></graphic></fig><p>Then we inoculated MDA-MB-231LN expressing luciferase into the m.f.p on the right side of the abdomen of a female mouse, and treated it with sunitinib at 40 mg/kg once a day, and DC101, an antibody for mouse VEGFR-2, at 800 μg/mouse for 2 consecutive weeks. In both groups of treated mice, tumor growth was significantly impeded (Figure <xref ref-type="fig" rid="F4">4b</xref>).</p></sec><sec><title>Sunitinib inhibits lymphangiogenesis and lymph node metastasis</title><p>Next, we examined the effect of sunitinib on angiogenesis and lymphangiogenesis by immunohistochemical analysis. The density of blood vessels stained with anti-CD31 in the primary tumor was significantly reduced, to almost the same degree, by treatment with sunitinib and DC101 (Figure <xref ref-type="fig" rid="F5">5a, b</xref>). The number of lymphatic vessels, stained with anti-LYVE-1, was also reduced by this treatment. Sunitinib was more potent than DC101 in reducing the number of lymphatic vessels (Figure <xref ref-type="fig" rid="F5">5a, b</xref>).</p><fig id="F5" position="float"><label>Figure 5</label><caption><p><bold>Sunitinib inhibited angiogenesis, lymphangiogenesis, and lymph node metastasis in the m.f.p. model</bold>. <bold>(a) </bold>Immunohistochemical analysis of the primary tumor treated with sunitinib, DC101, or vehicle. Tumors were stained with anti-CD31 for endothelial cells (upper) and anti-LYVE-1 for lymphatic endothelial cells (lower). Photographs were taken under a microscope at a magnification of ×8. Photographs of representative areas are shown. The black line represents 50 μm. <bold>(b) </bold>Effects of sunitinib and DC101 on tumor angiogenesis and lymphangiogenesis. The microvessel density (MVD, top) was determined by staining for CD31, and the lymphatic microvessel density (LVD, bottom) by staining for LYVE-1. *<italic>P </italic>< 0.05 as compared with control. <bold>(c) </bold>Lymph node metastasis was detected by bioluminescent imaging <italic>in vivo</italic>. The primary tumor (left) was identified on day 1 of treatment, and tumor metastasis around the axillary lymph node was detected after treatment with vehicle control (right, upper) or sunitinib (right, lower). <italic>Ex vivo </italic>data of the lymph nodes confirmed metastasis from the MDA-MB-231LN primary tumor. Three representative photographs from each treatment group are shown. LVD, lymphatic microvessel density; m.f.p., mammary fat pad; MVD, microvessel density.</p></caption><graphic xlink:href="bcr2903-5"></graphic></fig><p>Then, the lymph node metastases were analyzed by bioluminescent imaging. Although previously, it was difficult to detect metastasis in living mice, development of luciferase and the bioluminescent technology has now enabled the detection of cancer cells in distant organs. Bioluminescent signals from the primary tumor in the m.f.p on the right side of the abdomen were observed on day 0 (Figure <xref ref-type="fig" rid="F5">5c</xref>, left panel). Signals from the cells metastasized around the axillary lymph node (right side) were detected in all the mice of the control group at day 14 (Figure <xref ref-type="fig" rid="F5">5c</xref>, right panels). Metastasis in the lymph node was confirmed by <italic>ex vivo </italic>imaging after resection. Lymph node metastasis on the opposite side (left side) was also observed in 6 mice from the control group; however, no metastases were recognized in the mandibular or mesenteric lymph nodes (data not shown). Metastasis to the axillary lymph node appears to occur in the early stage of the metastatic phase in this model.</p><p>Sunitinib strongly inhibited the development of axillary lymph node metastasis on the same side as the tumor (right side), although some of the mice showed metastasis (Table <xref ref-type="table" rid="T1">1</xref>). Metastasis to the lung was also reduced (Table <xref ref-type="table" rid="T1">1</xref>, Additional data file <xref ref-type="supplementary-material" rid="S3">3</xref>). DC101 tended to reduce metastasis; however, the effect was weak as compared with that of sunitinib.</p><table-wrap id="T1" position="float"><label>Table 1</label><caption><p>Effect of sunitinib and DC101 on axillary lymph node and lung metastasis from MDA-MB-231LN in the m.f.p. model</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left">Treatment</th><th align="left">Axillary lymph node metastases (right, left)</th><th align="left">Lung metastases</th></tr></thead><tbody><tr><td align="left">Control</td><td align="left">14/14 (13, 6)</td><td align="left">12/14</td></tr><tr><td align="left">DC101</td><td align="left">10/15 (10, 1)</td><td align="left">9/15</td></tr><tr><td align="left">Sunitinib</td><td align="left">5/15<sup>a </sup>(5, 0)</td><td align="left">3/15<sup>a</sup></td></tr></tbody></table><table-wrap-foot><p>In the experiment illustrated in Figure 5, axillary lymph node and lung metastases were confirmed by bioluminescent imaging <italic>ex vivo</italic>. Values are shown as the number of mice with metastasis in each organ. The statistical analysis is described in the Materials and Methods section. The results were considered to be statistically significant at <italic>P </italic>< 0.05. <sup>a</sup><italic>P </italic>< 0.05 as compared with control.</p></table-wrap-foot></table-wrap></sec></sec><sec><title>Discussion</title><p>Sunitinib is well-known as an inhibitor of angiogenesis and to exert activity against VEGFR2. In this study, we demonstrated that sunitinib inhibited the activation of VEGFR2/3 signaling and of the downstream molecules MEK, Erk, and Akt induced by VEGF-C and VEGF-D in lymphatic endothelial cells. Consequently, sunitinib blocked the cellular functions of the LECs, such as growth, migration and tube formation. Thus, sunitinib is actually a dual inhibitor of VEGFR2 and VEGFR3.</p><p>VEGFR-3 plays a pivotal role in lymphatic vascular formation, and VEGFR-3 inhibition by antibody has been shown to disrupt the cellular functions of LECs and adult lymphangiogenesis [<xref ref-type="bibr" rid="B18">18</xref>]. On the other hand, the role of VRGFR2 in the development of lymphatic vessels is not well clarified. However, VEGFR-2 is coexpressed and forms a heterodimer with VEGFR-3 in lymphatic endothelial cells [<xref ref-type="bibr" rid="B28">28</xref>] and the two molecules function together in inducing angiogenic sprouting [<xref ref-type="bibr" rid="B29">29</xref>]. Consistent with this mechanism, VEGFR2 and VEGFR3 in LECs are activated concurrently by VEGFC/D stimulation. In addition, anti-VEGFR2 antibody partially suppressed the functions of LECs and tumor lymphangiogenesis in the mouse model. VEGFR-2 could be involved in lymphangiogenesis through its direct effect on the LECs. Collectively, suppression of either VEGFR-2 or VEGFR-3 alone might not be sufficient to inhibit cellular signaling and lymphangiogenesis. Other multi-VEGFR inhibitors such as cediranib and PTK787 have also been demonstrated to show a suppressive effect on lymphangiogenesis [<xref ref-type="bibr" rid="B23">23</xref>,<xref ref-type="bibr" rid="B24">24</xref>]. Similarly, the dual inhibition of VEGFR-2 and VEGFR-3 by sunitinib might be important for the activity of this drug against the cellular functions of LECs and lymphangiogenesis.</p><p>Our results of the animal experiment imply that sunitinib might be of benefit in the treatment of breast cancer by suppressing lymph node metastasis. In clinical settings, lymph node metastasis is a useful marker of the prognosis of breast cancer and a determinant factor of systemic chemotherapy in a neoadjuvant setting; moreover, lymph node dissection prolongs the survival of patients with a positive sentinel lymph node. The main mechanism underlying this effect is thought to be suppression of the formation of lymphatic vessels as escape routes to neighboring lymph nodes. Furthermore, a new supportive role of lymph nodes for cancer cell survival in lymphatic organs has been proposed recently, and certain cancer cells seem to move toward distant sites via lymph nodes in the vicinity [<xref ref-type="bibr" rid="B5">5</xref>]. Given that the incidence of lung metastasis was also reduced by sunitinib treatment, restricting metastasis to regional lymph nodes might be useful to suppress systemic dissemination.</p><p>VEGFR pathways are attractive targets in cancer therapeutics, since the activities of the ligands and receptors can be controlled by specific antibodies or small-molecule inhibitors, including sunitinib. Also, the invasion-promoting role of VEGFRs in cancer cells has been reported recently [<xref ref-type="bibr" rid="B30">30</xref>]. Actually, numerous studies have shown that VEGFR inhibitors can suppress tumor growth and distant metastasis [<xref ref-type="bibr" rid="B31">31</xref>,<xref ref-type="bibr" rid="B32">32</xref>]. However, recently, two groups have also reported that short-term treatment with sunitinib promotes metastasis in mice [<xref ref-type="bibr" rid="B33">33</xref>,<xref ref-type="bibr" rid="B34">34</xref>]. These previous data and our present study data suggest that angiogenesis inhibitors and angiogenic therapy could affect tumor metastasis both positively and negatively depending on the drug dosing schedule or the therapeutic setting, although the precise underlying mechanisms remain unclear. Angiogenesis, lymphangiogenesis and metastasis are intricate processes involving not only numerous molecules, but also various physiologic responses. These mechanisms should be further investigated to develop better therapeutic use of inhibitors of angiogenesis and lymphangiogenesis.</p></sec><sec><title>Conclusions</title><p>In this study, we demonstrated that sunitinib inhibited VEGFR-3 and VEGFR-2 signaling under VEGF-C or VEGF-D stimulation, and that it interfered with the cellular functions of LECs induced by VEGF-C, thereby inhibiting lymphangiogenesis and lymph node metastasis in a breast cancer model. In particular, we showed that inhibition of VEGFR-3 might be essential for these effects of sunitinib. Our findings suggest that sunitinib might be of benefit in the treatment of breast cancer by suppressing lymphangiogenesis and lymph node metastasis.</p></sec><sec><title>Abbreviations</title><p>DMSO: dimethyl sulfoxide; ERK1/2: extracellular signal-regulated kinase 1/2; LEC: lymphatic endothelial cell; m.f.p: mammary fat pad; VEGF: vascular endothelial growth factor; VEGFR: vascular endothelial growth factor receptor.</p></sec><sec><title>Competing interests</title><p>The authors declare that they have no competing interests.</p></sec><sec><title>Authors' contributions</title><p>YKo is the first author of this article, conceived the study, organized it, and collected the data. YKa participated in the design of the immunologic assay. YKi collected some data related to the cellular assay. TH participated in the design of the immunohistochemical analysis and contributed to the analysis itself. KN participated in the design of this entire study and contributed to the interpretation of the results. TT participated in and contributed to the interpretation of the results. Fumiaki Koizumi participated in study design and coordination, helped draft the manuscript, and provided final approval for the version to be published. All the authors read and approved the final manuscript.</p></sec><sec sec-type="supplementary-material"><title>Supplementary Material</title><supplementary-material content-type="local-data" id="S1"><caption><title>Additional file 1</title><p><bold>Figure S1. effect of sunitinib on the signaling molecules ras, c-Raf, and MEK in the LECs, and the dose-dependent effect of anti-VEGFR-2 on VEGFR-2 phosphorylation</bold>. Western blotting was performed, as shown in Figure <xref ref-type="fig" rid="F1">1</xref>. Although sunitinib did not affect the degree of phosphorylation of ras or c-Raf, it suppressed MEK phosphorylation <bold>(a)</bold>. LECs were treated with anti-VEGFR-2 (0, 0.2, 2. or 5 μg) under VEGF-C stimulation <bold>(b)</bold>. The inhibitory effect of the antibody was saturated at the antibody dose of 2 μg.</p></caption><media xlink:href="bcr2903-S1.TIFF" mimetype="image" mime-subtype="tiff"><caption><p>Click here for file</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="S2"><caption><title>Additional file 2</title><p><bold>Figure S2. Quantification of protein phosphorylations induced by VEGF-C/D</bold>. Western blotting data (Figure <xref ref-type="fig" rid="F1">1</xref>) were captured and quantified by the imaging software, MultiGauge (Fujifilm). The amounts of phosphorylated protein were divided by those of total protein. Each phosphorylation ratio was normalized to that in the nontreated controls.</p></caption><media xlink:href="bcr2903-S2.TIFF" mimetype="image" mime-subtype="tiff"><caption><p>Click here for file</p></caption></media></supplementary-material><supplementary-material content-type="local-data" id="S3"><caption><title>Additional file 3</title><p><bold>Figure S3. Lung metastasis was detected after treatment with vehicle control (upper) or sunitinib (lower)</bold>. Representative photographs of three <italic>ex vivo </italic>data from each treatment group are shown.</p></caption><media xlink:href="bcr2903-S3.TIFF" mimetype="image" mime-subtype="tiff"><caption><p>Click here for file</p></caption></media></supplementary-material></sec></body><back><sec><title>Acknowledgements</title><p>This work was supported in part by the Third-Term Comprehensive 10-Year Strategy for Cancer Control.</p></sec><ref-list><ref id="B1"><mixed-citation publication-type="journal"><name><surname>Gupta</surname><given-names>GP</given-names></name><name><surname>Massague</surname><given-names>J</given-names></name><article-title>Cancer metastasis: building a framework</article-title><source>Cell</source><year>2006</year><volume>127</volume><fpage>679</fpage><lpage>695</lpage><pub-id pub-id-type="doi">10.1016/j.cell.2006.11.001</pub-id><pub-id pub-id-type="pmid">17110329</pub-id></mixed-citation></ref><ref id="B2"><mixed-citation publication-type="journal"><name><surname>Stacker</surname><given-names>SA</given-names></name><name><surname>Achen</surname><given-names>MG</given-names></name><name><surname>Jussila</surname><given-names>L</given-names></name><name><surname>Baldwin</surname><given-names>ME</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><article-title>Lymphangiogenesis and cancer metastasis</article-title><source>Nat Rev Cancer</source><year>2002</year><volume>2</volume><fpage>573</fpage><lpage>583</lpage><pub-id pub-id-type="doi">10.1038/nrc863</pub-id><pub-id pub-id-type="pmid">12154350</pub-id></mixed-citation></ref><ref id="B3"><mixed-citation publication-type="journal"><name><surname>Alitalo</surname><given-names>K</given-names></name><name><surname>Tammela</surname><given-names>T</given-names></name><name><surname>Petrova</surname><given-names>TV</given-names></name><article-title>Lymphangiogenesis in development and human disease</article-title><source>Nature</source><year>2005</year><volume>438</volume><fpage>946</fpage><lpage>953</lpage><pub-id pub-id-type="doi">10.1038/nature04480</pub-id><pub-id pub-id-type="pmid">16355212</pub-id></mixed-citation></ref><ref id="B4"><mixed-citation publication-type="journal"><name><surname>Joyce</surname><given-names>JA</given-names></name><name><surname>Pollard</surname><given-names>JW</given-names></name><article-title>Microenvironmental regulation of metastasis</article-title><source>Nat Rev Cancer</source><year>2009</year><volume>9</volume><fpage>239</fpage><lpage>252</lpage><pub-id pub-id-type="doi">10.1038/nrc2618</pub-id><pub-id pub-id-type="pmid">19279573</pub-id></mixed-citation></ref><ref id="B5"><mixed-citation publication-type="journal"><name><surname>Tammela</surname><given-names>T</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><article-title>Lymphangiogenesis: molecular mechanisms and future promise</article-title><source>Cell</source><year>2010</year><volume>140</volume><fpage>460</fpage><lpage>476</lpage><pub-id pub-id-type="doi">10.1016/j.cell.2010.01.045</pub-id><pub-id pub-id-type="pmid">20178740</pub-id><pub-id pub-id-type="pmid">20178740</pub-id></mixed-citation></ref><ref id="B6"><mixed-citation publication-type="journal"><name><surname>Achen</surname><given-names>MG</given-names></name><name><surname>McColl</surname><given-names>BK</given-names></name><name><surname>Stacker</surname><given-names>SA</given-names></name><article-title>Focus on lymphangiogenesis in tumor metastasis</article-title><source>Cancer Cell</source><year>2005</year><volume>7</volume><fpage>121</fpage><lpage>127</lpage><pub-id pub-id-type="doi">10.1016/j.ccr.2005.01.017</pub-id><pub-id pub-id-type="pmid">15710325</pub-id></mixed-citation></ref><ref id="B7"><mixed-citation publication-type="journal"><name><surname>Adams</surname><given-names>RH</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><article-title>Molecular regulation of angiogenesis and lymphangiogenesis</article-title><source>Nat Rev Mol Cell Biol</source><year>2007</year><volume>8</volume><fpage>464</fpage><lpage>478</lpage><pub-id pub-id-type="doi">10.1038/nrm2183</pub-id><pub-id pub-id-type="pmid">17522591</pub-id></mixed-citation></ref><ref id="B8"><mixed-citation publication-type="journal"><name><surname>Zwaans</surname><given-names>BM</given-names></name><name><surname>Bielenberg</surname><given-names>DR</given-names></name><article-title>Potential therapeutic strategies for lymphatic metastasis</article-title><source>Microvasc Res</source><year>2007</year><volume>74</volume><fpage>145</fpage><lpage>158</lpage><pub-id pub-id-type="doi">10.1016/j.mvr.2007.08.006</pub-id><pub-id pub-id-type="pmid">17950368</pub-id></mixed-citation></ref><ref id="B9"><mixed-citation publication-type="journal"><name><surname>Skobe</surname><given-names>M</given-names></name><name><surname>Hawighorst</surname><given-names>T</given-names></name><name><surname>Jackson</surname><given-names>DG</given-names></name><name><surname>Prevo</surname><given-names>R</given-names></name><name><surname>Janes</surname><given-names>L</given-names></name><name><surname>Velasco</surname><given-names>P</given-names></name><name><surname>Riccardi</surname><given-names>L</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><name><surname>Claffey</surname><given-names>K</given-names></name><name><surname>Detmar</surname><given-names>M</given-names></name><article-title>Induction of tumor lymphangiogenesis by VEGF-C promotes breast cancer metastasis</article-title><source>Nat Med</source><year>2001</year><volume>7</volume><fpage>192</fpage><lpage>198</lpage><pub-id pub-id-type="doi">10.1038/84643</pub-id><pub-id pub-id-type="pmid">11175850</pub-id></mixed-citation></ref><ref id="B10"><mixed-citation publication-type="journal"><name><surname>Stacker</surname><given-names>SA</given-names></name><name><surname>Caesar</surname><given-names>C</given-names></name><name><surname>Baldwin</surname><given-names>ME</given-names></name><name><surname>Thornton</surname><given-names>GE</given-names></name><name><surname>Williams</surname><given-names>RA</given-names></name><name><surname>Prevo</surname><given-names>R</given-names></name><name><surname>Jackson</surname><given-names>DG</given-names></name><name><surname>Nishikawa</surname><given-names>S</given-names></name><name><surname>Kubo</surname><given-names>H</given-names></name><name><surname>Achen</surname><given-names>MG</given-names></name><article-title>VEGF-D promotes the metastatic spread of tumor cells via the lymphatics</article-title><source>Nat Med</source><year>2001</year><volume>7</volume><fpage>186</fpage><lpage>191</lpage><pub-id pub-id-type="doi">10.1038/84635</pub-id><pub-id pub-id-type="pmid">11175849</pub-id></mixed-citation></ref><ref id="B11"><mixed-citation publication-type="journal"><name><surname>Podgrabinska</surname><given-names>S</given-names></name><name><surname>Braun</surname><given-names>P</given-names></name><name><surname>Velasco</surname><given-names>P</given-names></name><name><surname>Kloos</surname><given-names>B</given-names></name><name><surname>Pepper</surname><given-names>MS</given-names></name><name><surname>Skobe</surname><given-names>M</given-names></name><article-title>Molecular characterization of lymphatic endothelial cells</article-title><source>Proc Natl Acad Sci USA</source><year>2002</year><volume>99</volume><fpage>16069</fpage><lpage>16074</lpage><pub-id pub-id-type="doi">10.1073/pnas.242401399</pub-id><pub-id pub-id-type="pmid">12446836</pub-id></mixed-citation></ref><ref id="B12"><mixed-citation publication-type="journal"><name><surname>Zeng</surname><given-names>Y</given-names></name><name><surname>Opeskin</surname><given-names>K</given-names></name><name><surname>Goad</surname><given-names>J</given-names></name><name><surname>Williams</surname><given-names>ED</given-names></name><article-title>Tumor-induced activation of lymphatic endothelial cells via vascular endothelial growth factor receptor-2 is critical for prostate cancer lymphatic metastasis</article-title><source>Cancer Res</source><year>2006</year><volume>66</volume><fpage>9566</fpage><lpage>9575</lpage><pub-id pub-id-type="doi">10.1158/0008-5472.CAN-06-1488</pub-id><pub-id pub-id-type="pmid">17018613</pub-id></mixed-citation></ref><ref id="B13"><mixed-citation publication-type="journal"><name><surname>Wissmann</surname><given-names>C</given-names></name><name><surname>Detmar</surname><given-names>M</given-names></name><article-title>Pathways targeting tumor lymphangiogenesis</article-title><source>Clin Cancer Res</source><year>2006</year><volume>12</volume><fpage>6865</fpage><lpage>6868</lpage><pub-id pub-id-type="doi">10.1158/1078-0432.CCR-06-1800</pub-id><pub-id pub-id-type="pmid">17145802</pub-id></mixed-citation></ref><ref id="B14"><mixed-citation publication-type="journal"><name><surname>Dumont</surname><given-names>DJ</given-names></name><name><surname>Jussila</surname><given-names>L</given-names></name><name><surname>Taipale</surname><given-names>J</given-names></name><name><surname>Lymboussaki</surname><given-names>A</given-names></name><name><surname>Mustonen</surname><given-names>T</given-names></name><name><surname>Pajusola</surname><given-names>K</given-names></name><name><surname>Breitman</surname><given-names>M</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><article-title>Cardiovascular failure in mouse embryos deficient in VEGF receptor-3</article-title><source>Science</source><year>1998</year><volume>282</volume><fpage>946</fpage><lpage>949</lpage><pub-id pub-id-type="pmid">9794766</pub-id></mixed-citation></ref><ref id="B15"><mixed-citation publication-type="journal"><name><surname>Mäkinen</surname><given-names>T</given-names></name><name><surname>Jussila</surname><given-names>L</given-names></name><name><surname>Veikkola</surname><given-names>T</given-names></name><name><surname>Karpanen</surname><given-names>T</given-names></name><name><surname>Kettunen</surname><given-names>MI</given-names></name><name><surname>Pulkkanen</surname><given-names>KJ</given-names></name><name><surname>Kauppinen</surname><given-names>R</given-names></name><name><surname>Jackson</surname><given-names>DG</given-names></name><name><surname>Kubo</surname><given-names>H</given-names></name><name><surname>Nishikawa</surname><given-names>S</given-names></name><name><surname>Ylä-Herttuala</surname><given-names>S</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><article-title>Inhibition of lymphangiogenesis with resulting lymphedema in transgenic mice expressing soluble VEGF receptor-3</article-title><source>Nat Med</source><year>2001</year><volume>7</volume><fpage>199</fpage><lpage>205</lpage><pub-id pub-id-type="doi">10.1038/84651</pub-id><pub-id pub-id-type="pmid">11175851</pub-id></mixed-citation></ref><ref id="B16"><mixed-citation publication-type="journal"><name><surname>Kriehuber</surname><given-names>E</given-names></name><name><surname>Breiteneder-Geleff</surname><given-names>S</given-names></name><name><surname>Groeger</surname><given-names>M</given-names></name><name><surname>Soleiman</surname><given-names>A</given-names></name><name><surname>Schoppmann</surname><given-names>SF</given-names></name><name><surname>Stingl</surname><given-names>G</given-names></name><name><surname>Kerjaschki</surname><given-names>D</given-names></name><name><surname>Maurer</surname><given-names>D</given-names></name><article-title>Isolation and characterization of dermal lymphatic and blood endothelial cells reveal stable and functionally specialized cell lineages</article-title><source>J Exp Med</source><year>2001</year><volume>194</volume><fpage>797</fpage><lpage>808</lpage><pub-id pub-id-type="doi">10.1084/jem.194.6.797</pub-id><pub-id pub-id-type="pmid">11560995</pub-id></mixed-citation></ref><ref id="B17"><mixed-citation publication-type="journal"><name><surname>Saaristo</surname><given-names>A</given-names></name><name><surname>Veikkola</surname><given-names>T</given-names></name><name><surname>Enholm</surname><given-names>B</given-names></name><name><surname>Hytönen</surname><given-names>M</given-names></name><name><surname>Arola</surname><given-names>J</given-names></name><name><surname>Pajusola</surname><given-names>K</given-names></name><name><surname>Turunen</surname><given-names>P</given-names></name><name><surname>Jeltsch</surname><given-names>M</given-names></name><name><surname>Karkkainen</surname><given-names>MJ</given-names></name><name><surname>Kerjaschki</surname><given-names>D</given-names></name><name><surname>Bueler</surname><given-names>H</given-names></name><name><surname>Ylä-Herttuala</surname><given-names>S</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><article-title>Adenoviral VEGF-C overexpression induces blood vessel enlargement, tortuosity, and leakiness but no sprouting angiogenesis in the skin or mucous membranes</article-title><source>Faseb J</source><year>2002</year><volume>16</volume><fpage>1041</fpage><lpage>1049</lpage><pub-id pub-id-type="doi">10.1096/fj.01-1042com</pub-id><pub-id pub-id-type="pmid">12087065</pub-id></mixed-citation></ref><ref id="B18"><mixed-citation publication-type="journal"><name><surname>Goldman</surname><given-names>J</given-names></name><name><surname>Rutkowski</surname><given-names>JM</given-names></name><name><surname>Shields</surname><given-names>JD</given-names></name><name><surname>Pasquier</surname><given-names>MC</given-names></name><name><surname>Cui</surname><given-names>Y</given-names></name><name><surname>Schmokel</surname><given-names>HG</given-names></name><name><surname>Willey</surname><given-names>S</given-names></name><name><surname>Hicklin</surname><given-names>DJ</given-names></name><name><surname>Pytowski</surname><given-names>B</given-names></name><name><surname>Swartz</surname><given-names>MA</given-names></name><article-title>Cooperative and redundant roles of VEGFR-2 and VEGFR-3 signaling in adult lymphangiogenesis</article-title><source>FASEB J</source><year>2007</year><volume>21</volume><fpage>1003</fpage><lpage>1012</lpage><pub-id pub-id-type="doi">10.1096/fj.06-6656com</pub-id><pub-id pub-id-type="pmid">17210781</pub-id></mixed-citation></ref><ref id="B19"><mixed-citation publication-type="journal"><name><surname>He</surname><given-names>Y</given-names></name><name><surname>Kozaki</surname><given-names>K</given-names></name><name><surname>Karpanen</surname><given-names>T</given-names></name><name><surname>Koshikawa</surname><given-names>K</given-names></name><name><surname>Yla-Herttuala</surname><given-names>S</given-names></name><name><surname>Takahashi</surname><given-names>T</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><article-title>Suppression of tumor lymphangiogenesis and lymph node metastasis by blocking vascular endothelial growth factor receptor 3 signaling</article-title><source>J Natl Cancer Inst</source><year>2002</year><volume>94</volume><fpage>819</fpage><lpage>825</lpage><pub-id pub-id-type="pmid">12048269</pub-id></mixed-citation></ref><ref id="B20"><mixed-citation publication-type="journal"><name><surname>Roberts</surname><given-names>N</given-names></name><name><surname>Kloos</surname><given-names>B</given-names></name><name><surname>Cassella</surname><given-names>M</given-names></name><name><surname>Podgrabinska</surname><given-names>S</given-names></name><name><surname>Persaud</surname><given-names>K</given-names></name><name><surname>Wu</surname><given-names>Y</given-names></name><name><surname>Pytowski</surname><given-names>B</given-names></name><name><surname>Skobe</surname><given-names>M</given-names></name><article-title>Inhibition of VEGFR-3 activation with the antagonistic antibody more potently suppresses lymph node and distant metastases than inactivation of VEGFR-2</article-title><source>Cancer Res</source><year>2006</year><volume>66</volume><fpage>2650</fpage><lpage>2657</lpage><pub-id pub-id-type="doi">10.1158/0008-5472.CAN-05-1843</pub-id><pub-id pub-id-type="pmid">16510584</pub-id></mixed-citation></ref><ref id="B21"><mixed-citation publication-type="journal"><name><surname>Burton</surname><given-names>JB</given-names></name><name><surname>Priceman</surname><given-names>SJ</given-names></name><name><surname>Sung</surname><given-names>JL</given-names></name><name><surname>Brakenhielm</surname><given-names>E</given-names></name><name><surname>An</surname><given-names>DS</given-names></name><name><surname>Pytowski</surname><given-names>B</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><name><surname>Wu</surname><given-names>L</given-names></name><article-title>Suppression of prostate cancer nodal and systemic metastasis by blockade of the lymphangiogenic axis</article-title><source>Cancer Res</source><year>2008</year><volume>68</volume><fpage>7828</fpage><lpage>7837</lpage><pub-id pub-id-type="doi">10.1158/0008-5472.CAN-08-1488</pub-id><pub-id pub-id-type="pmid">18829538</pub-id></mixed-citation></ref><ref id="B22"><mixed-citation publication-type="journal"><name><surname>Matsui</surname><given-names>J</given-names></name><name><surname>Funahashi</surname><given-names>Y</given-names></name><name><surname>Uenaka</surname><given-names>T</given-names></name><name><surname>Watanabe</surname><given-names>T</given-names></name><name><surname>Tsuruoka</surname><given-names>A</given-names></name><name><surname>Asada</surname><given-names>M</given-names></name><article-title>Multi-kinase inhibitor E7080 suppresses lymph node and lung metastases of human mammary breast tumor MDA-MB-231 via inhibition of vascular endothelial growth factor-receptor (VEGF-R) 2 and VEGF-R3 kinase</article-title><source>Clin Cancer Res</source><year>2008</year><volume>14</volume><fpage>5459</fpage><lpage>5465</lpage><pub-id pub-id-type="doi">10.1158/1078-0432.CCR-07-5270</pub-id><pub-id pub-id-type="pmid">18765537</pub-id></mixed-citation></ref><ref id="B23"><mixed-citation publication-type="journal"><name><surname>Heckman</surname><given-names>CA</given-names></name><name><surname>Holopainen</surname><given-names>T</given-names></name><name><surname>Wirzenius</surname><given-names>M</given-names></name><name><surname>Keskitalo</surname><given-names>S</given-names></name><name><surname>Jeltsch</surname><given-names>M</given-names></name><name><surname>Yla-Herttuala</surname><given-names>S</given-names></name><name><surname>Wedge</surname><given-names>SR</given-names></name><name><surname>Jurgensmeier</surname><given-names>JM</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><article-title>The tyrosine kinase inhibitor cediranib blocks ligand-induced vascular endothelial growth factor receptor-3 activity and lymphangiogenesis</article-title><source>Cancer Res</source><year>2008</year><volume>68</volume><fpage>4754</fpage><lpage>4762</lpage><pub-id pub-id-type="doi">10.1158/0008-5472.CAN-07-5809</pub-id><pub-id pub-id-type="pmid">18559522</pub-id></mixed-citation></ref><ref id="B24"><mixed-citation publication-type="journal"><name><surname>Schomber</surname><given-names>T</given-names></name><name><surname>Zumsteg</surname><given-names>A</given-names></name><name><surname>Strittmatter</surname><given-names>K</given-names></name><name><surname>Crnic</surname><given-names>I</given-names></name><name><surname>Antoniadis</surname><given-names>H</given-names></name><name><surname>Littlewood-Evans</surname><given-names>A</given-names></name><name><surname>Wood</surname><given-names>J</given-names></name><name><surname>Christofori</surname><given-names>G</given-names></name><article-title>Differential effects of the vascular endothelial growth factor receptor inhibitor PTK787/ZK222584 on tumor angiogenesis and tumor lymphangiogenesis</article-title><source>Mol Cancer Ther</source><year>2009</year><volume>8</volume><fpage>55</fpage><lpage>63</lpage><pub-id pub-id-type="doi">10.1158/1535-7163.MCT-08-0679</pub-id><pub-id pub-id-type="pmid">19139113</pub-id></mixed-citation></ref><ref id="B25"><mixed-citation publication-type="journal"><name><surname>Faivre</surname><given-names>S</given-names></name><name><surname>Demetri</surname><given-names>G</given-names></name><name><surname>Sargent</surname><given-names>W</given-names></name><name><surname>Raymond</surname><given-names>E</given-names></name><article-title>Molecular basis for sunitinib efficacy and future clinical development</article-title><source>Nat Rev Drug Discov</source><year>2007</year><volume>6</volume><fpage>734</fpage><lpage>745</lpage><pub-id pub-id-type="doi">10.1038/nrd2380</pub-id><pub-id pub-id-type="pmid">17690708</pub-id></mixed-citation></ref><ref id="B26"><mixed-citation publication-type="journal"><name><surname>Jenkins</surname><given-names>DE</given-names></name><name><surname>Hornig</surname><given-names>YS</given-names></name><name><surname>Oei</surname><given-names>Y</given-names></name><name><surname>Dusich</surname><given-names>J</given-names></name><name><surname>Purchio</surname><given-names>T</given-names></name><article-title>Bioluminescent human breast cancer cell lines that permit rapid and sensitive in vivo detection of mammary tumors and multiple metastases in immune deficient mice</article-title><source>Breast Cancer Res</source><year>2005</year><volume>7</volume><fpage>R444</fpage><lpage>454</lpage><pub-id pub-id-type="doi">10.1186/bcr1026</pub-id><pub-id pub-id-type="pmid">15987449</pub-id></mixed-citation></ref><ref id="B27"><mixed-citation publication-type="journal"><name><surname>Fukai</surname><given-names>J</given-names></name><name><surname>Nishio</surname><given-names>K</given-names></name><name><surname>Itakura</surname><given-names>T</given-names></name><name><surname>Koizumi</surname><given-names>F</given-names></name><article-title>Antitumor activity of cetuximab against malignant glioma cells overexpressing EGFR deletion mutant variant III</article-title><source>Cancer Sci</source><year>2008</year><volume>99</volume><fpage>2062</fpage><lpage>2069</lpage><pub-id pub-id-type="pmid">19016767</pub-id></mixed-citation></ref><ref id="B28"><mixed-citation publication-type="journal"><name><surname>Dixelius</surname><given-names>J</given-names></name><name><surname>Makinen</surname><given-names>T</given-names></name><name><surname>Wirzenius</surname><given-names>M</given-names></name><name><surname>Karkkainen</surname><given-names>MJ</given-names></name><name><surname>Wernstedt</surname><given-names>C</given-names></name><name><surname>Alitalo</surname><given-names>K</given-names></name><name><surname>Claesson-Welsh</surname><given-names>L</given-names></name><article-title>Ligand-induced vascular endothelial growth factor receptor-3 (VEGFR-3) heterodimerization with VEGFR-2 in primary lymphatic endothelial cells regulates tyrosine phosphorylation sites</article-title><source>J Biol Chem</source><year>2003</year><volume>278</volume><fpage>40973</fpage><lpage>40979</lpage><pub-id pub-id-type="doi">10.1074/jbc.M304499200</pub-id><pub-id pub-id-type="pmid">12881528</pub-id></mixed-citation></ref><ref id="B29"><mixed-citation publication-type="journal"><name><surname>Alam</surname><given-names>A</given-names></name><name><surname>Herault</surname><given-names>JP</given-names></name><name><surname>Barron</surname><given-names>P</given-names></name><name><surname>Favier</surname><given-names>B</given-names></name><name><surname>Fons</surname><given-names>P</given-names></name><name><surname>Delesque-Touchard</surname><given-names>N</given-names></name><name><surname>Senegas</surname><given-names>I</given-names></name><name><surname>Laboudie</surname><given-names>P</given-names></name><name><surname>Bonnin</surname><given-names>J</given-names></name><name><surname>Cassan</surname><given-names>C</given-names></name><name><surname>Savi</surname><given-names>P</given-names></name><name><surname>Ruggeri</surname><given-names>B</given-names></name><name><surname>Carmeliet</surname><given-names>P</given-names></name><name><surname>Bono</surname><given-names>F</given-names></name><name><surname>Herbert</surname><given-names>JM</given-names></name><article-title>Heterodimerization with vascular endothelial growth factor receptor-2 (VEGFR-2) is necessary for VEGFR-3 activity</article-title><source>Biochem Biophys Res Commun</source><year>2004</year><volume>324</volume><fpage>909</fpage><lpage>915</lpage><pub-id pub-id-type="doi">10.1016/j.bbrc.2004.08.237</pub-id><pub-id pub-id-type="pmid">15474514</pub-id></mixed-citation></ref><ref id="B30"><mixed-citation publication-type="journal"><name><surname>Morelli</surname><given-names>MP</given-names></name><name><surname>Brown</surname><given-names>AM</given-names></name><name><surname>Pitts</surname><given-names>TM</given-names></name><name><surname>Tentler</surname><given-names>JJ</given-names></name><name><surname>Ciardiello</surname><given-names>F</given-names></name><name><surname>Ryan</surname><given-names>A</given-names></name><name><surname>Jurgensmeier</surname><given-names>JM</given-names></name><name><surname>Eckhardt</surname><given-names>SG</given-names></name><article-title>Targeting vascular endothelial growth factor receptor-1 and -3 with cediranib (AZD2171): effects on migration and invasion of gastrointestinal cancer cell lines</article-title><source>Mol Cancer Ther</source><year>2009</year><volume>8</volume><fpage>2546</fpage><lpage>2558</lpage><pub-id pub-id-type="doi">10.1158/1535-7163.MCT-09-0380</pub-id><pub-id pub-id-type="pmid">19755510</pub-id></mixed-citation></ref><ref id="B31"><mixed-citation publication-type="journal"><name><surname>Blansfield</surname><given-names>JA</given-names></name><name><surname>Caragacianu</surname><given-names>D</given-names></name><name><surname>Alexander</surname><given-names>HR</given-names></name><name><surname>Tangrea</surname><given-names>MA</given-names></name><name><surname>Morita</surname><given-names>SY</given-names></name><name><surname>Lorang</surname><given-names>D</given-names></name><name><surname>Schafer</surname><given-names>P</given-names></name><name><surname>Muller</surname><given-names>G</given-names></name><name><surname>Stirling</surname><given-names>D</given-names></name><name><surname>Royal</surname><given-names>RE</given-names></name><name><surname>Libutti</surname><given-names>SK</given-names></name><article-title>Combining agents that target the tumor microenvironment improves the efficacy of anticancer therapy</article-title><source>Clin Cancer Res</source><year>2008</year><volume>14</volume><fpage>270</fpage><lpage>280</lpage><pub-id pub-id-type="doi">10.1158/1078-0432.CCR-07-1562</pub-id><pub-id pub-id-type="pmid">18172279</pub-id></mixed-citation></ref><ref id="B32"><mixed-citation publication-type="journal"><name><surname>Zhang</surname><given-names>L</given-names></name><name><surname>Smith</surname><given-names>KM</given-names></name><name><surname>Chong</surname><given-names>AL</given-names></name><name><surname>Stempak</surname><given-names>D</given-names></name><name><surname>Yeger</surname><given-names>H</given-names></name><name><surname>Marrano</surname><given-names>P</given-names></name><name><surname>Thorner</surname><given-names>PS</given-names></name><name><surname>Irwin</surname><given-names>MS</given-names></name><name><surname>Kaplan</surname><given-names>DR</given-names></name><name><surname>Baruchel</surname><given-names>S</given-names></name><article-title>In vivo antitumor and antimetastatic activity of sunitinib in preclinical neuroblastoma mouse model</article-title><source>Neoplasia</source><year>2009</year><volume>11</volume><fpage>426</fpage><lpage>435</lpage><pub-id pub-id-type="pmid">19412427</pub-id></mixed-citation></ref><ref id="B33"><mixed-citation publication-type="journal"><name><surname>Ebos</surname><given-names>JM</given-names></name><name><surname>Lee</surname><given-names>CR</given-names></name><name><surname>Cruz-Munoz</surname><given-names>W</given-names></name><name><surname>Bjarnason</surname><given-names>GA</given-names></name><name><surname>Christensen</surname><given-names>JG</given-names></name><name><surname>Kerbel</surname><given-names>RS</given-names></name><article-title>Accelerated metastasis after short-term treatment with a potent inhibitor of tumor angiogenesis</article-title><source>Cancer Cell</source><year>2009</year><volume>15</volume><fpage>232</fpage><lpage>239</lpage><pub-id pub-id-type="doi">10.1016/j.ccr.2009.01.021</pub-id><pub-id pub-id-type="pmid">19249681</pub-id></mixed-citation></ref><ref id="B34"><mixed-citation publication-type="journal"><name><surname>Paez-Ribes</surname><given-names>M</given-names></name><name><surname>Allen</surname><given-names>E</given-names></name><name><surname>Hudock</surname><given-names>J</given-names></name><name><surname>Takeda</surname><given-names>T</given-names></name><name><surname>Okuyama</surname><given-names>H</given-names></name><name><surname>Vinals</surname><given-names>F</given-names></name><name><surname>Inoue</surname><given-names>M</given-names></name><name><surname>Bergers</surname><given-names>G</given-names></name><name><surname>Hanahan</surname><given-names>D</given-names></name><name><surname>Casanovas</surname><given-names>O</given-names></name><article-title>Antiangiogenic therapy elicits malignant progression of tumors to increased local invasion and distant metastasis</article-title><source>Cancer Cell</source><year>2009</year><volume>15</volume><fpage>220</fpage><lpage>231</lpage><pub-id pub-id-type="doi">10.1016/j.ccr.2009.01.027</pub-id><pub-id pub-id-type="pmid">19249680</pub-id></mixed-citation></ref></ref-list></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Pmc/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003C43 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 003C43 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Pmc
|étape= Corpus
|type= RBID
|clé= PMC:3218955
|texte= Sunitinib inhibits lymphatic endothelial cell functions and lymph node metastasis in a breast cancer model through inhibition of vascular endothelial growth factor receptor 3
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/RBID.i -Sk "pubmed:21693010" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd \
| NlmPubMed2Wicri -a LymphedemaV1
| This area was generated with Dilib version V0.6.31. |  |