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Biological Ablation of Sentinel Lymph Node Metastasis in Submucosally Invaded Early Gastrointestinal Cancer

Identifieur interne : 001469 ( Pmc/Checkpoint ); précédent : 001468; suivant : 001470

Biological Ablation of Sentinel Lymph Node Metastasis in Submucosally Invaded Early Gastrointestinal Cancer

Auteurs : Satoru Kikuchi [Japon] ; Hiroyuki Kishimoto [Japon] ; Hiroshi Tazawa [Japon] ; Yuuri Hashimoto [Japon] ; Shinji Kuroda [Japon] ; Masahiko Nishizaki [Japon] ; Takeshi Nagasaka [Japon] ; Yasuhiro Shirakawa [Japon] ; Shunsuke Kagawa [Japon] ; Yasuo Urata [Japon] ; Robert M. Hoffman [États-Unis] ; Toshiyoshi Fujiwara [Japon]

Source :

RBID : PMC:4351467

Abstract

Currently, early gastrointestinal cancers are treated endoscopically, as long as there are no lymph node metastases. However, once a gastrointestinal cancer invades the submucosal layer, the lymph node metastatic rate rises to higher than 10%. Therefore, surgery is still the gold standard to remove regional lymph nodes containing possible metastases. Here, to avoid prophylactic surgery, we propose a less-invasive biological ablation of lymph node metastasis in submucosally invaded gastrointestinal cancer patients. We have established an orthotopic early rectal cancer xenograft model with spontaneous lymph node metastasis by implantation of green fluorescent protein (GFP)-labeled human colon cancer cells into the submucosal layer of the murine rectum. A solution containing telomerase-specific oncolytic adenovirus was injected into the peritumoral submucosal space, followed by excision of the primary rectal tumors mimicking the endoscopic submucosal dissection (ESD) technique. Seven days after treatment, GFP signals had completely disappeared indicating that sentinel lymph node metastasis was selectively eradicated. Moreover, biologically treated mice were confirmed to be relapse-free even 4 weeks after treatment. These results indicate that virus-mediated biological ablation selectively targets lymph node metastasis and provides a potential alternative to surgery for submucosal invasive gastrointestinal cancer patients.


Url:
DOI: 10.1038/mt.2014.244
PubMed: 25523761
PubMed Central: 4351467


Affiliations:


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PMC:4351467

Le document en format XML

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<name sortKey="Nagasaka, Takeshi" sort="Nagasaka, Takeshi" uniqKey="Nagasaka T" first="Takeshi" last="Nagasaka">Takeshi Nagasaka</name>
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<p>Currently, early gastrointestinal cancers are treated endoscopically, as long as there are no lymph node metastases. However, once a gastrointestinal cancer invades the submucosal layer, the lymph node metastatic rate rises to higher than 10%. Therefore, surgery is still the gold standard to remove regional lymph nodes containing possible metastases. Here, to avoid prophylactic surgery, we propose a less-invasive biological ablation of lymph node metastasis in submucosally invaded gastrointestinal cancer patients. We have established an orthotopic early rectal cancer xenograft model with spontaneous lymph node metastasis by implantation of green fluorescent protein (GFP)-labeled human colon cancer cells into the submucosal layer of the murine rectum. A solution containing telomerase-specific oncolytic adenovirus was injected into the peritumoral submucosal space, followed by excision of the primary rectal tumors mimicking the endoscopic submucosal dissection (ESD) technique. Seven days after treatment, GFP signals had completely disappeared indicating that sentinel lymph node metastasis was selectively eradicated. Moreover, biologically treated mice were confirmed to be relapse-free even 4 weeks after treatment. These results indicate that virus-mediated biological ablation selectively targets lymph node metastasis and provides a potential alternative to surgery for submucosal invasive gastrointestinal cancer patients.</p>
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<name>
<surname>Kikuchi</surname>
<given-names>Satoru</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
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<name>
<surname>Kishimoto</surname>
<given-names>Hiroyuki</given-names>
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<xref ref-type="aff" rid="aff1">1</xref>
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<name>
<surname>Tazawa</surname>
<given-names>Hiroshi</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="aff" rid="aff2">2</xref>
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<surname>Hashimoto</surname>
<given-names>Yuuri</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kuroda</surname>
<given-names>Shinji</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
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<contrib contrib-type="author">
<name>
<surname>Nishizaki</surname>
<given-names>Masahiko</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
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<name>
<surname>Nagasaka</surname>
<given-names>Takeshi</given-names>
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<xref ref-type="aff" rid="aff1">1</xref>
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<name>
<surname>Shirakawa</surname>
<given-names>Yasuhiro</given-names>
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<xref ref-type="aff" rid="aff1">1</xref>
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<name>
<surname>Kagawa</surname>
<given-names>Shunsuke</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Urata</surname>
<given-names>Yasuo</given-names>
</name>
<xref ref-type="aff" rid="aff3">3</xref>
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<contrib contrib-type="author">
<name>
<surname>Hoffman</surname>
<given-names>Robert M</given-names>
</name>
<xref ref-type="aff" rid="aff4">4</xref>
<xref ref-type="aff" rid="aff5">5</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fujiwara</surname>
<given-names>Toshiyoshi</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="corresp" rid="caf1">*</xref>
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, Tokyo,
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</contrib-group>
<author-notes>
<corresp id="caf1">
<label>*</label>
Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama 700–8558, Japan. E-mail:
<email>toshi_f@md.okayama-u.ac.jp</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<month>03</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epreprint">
<day>19</day>
<month>12</month>
<year>2014</year>
</pub-date>
<pub-date pub-type="epub">
<day>20</day>
<month>01</month>
<year>2015</year>
</pub-date>
<volume>23</volume>
<issue>3</issue>
<fpage>501</fpage>
<lpage>509</lpage>
<history>
<date date-type="received">
<day>21</day>
<month>10</month>
<year>2014</year>
</date>
<date date-type="accepted">
<day>14</day>
<month>12</month>
<year>2014</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2015 American Society of Gene & Cell Therapy</copyright-statement>
<copyright-year>2015</copyright-year>
<copyright-holder>American Society of Gene & Cell Therapy</copyright-holder>
</permissions>
<abstract>
<p>Currently, early gastrointestinal cancers are treated endoscopically, as long as there are no lymph node metastases. However, once a gastrointestinal cancer invades the submucosal layer, the lymph node metastatic rate rises to higher than 10%. Therefore, surgery is still the gold standard to remove regional lymph nodes containing possible metastases. Here, to avoid prophylactic surgery, we propose a less-invasive biological ablation of lymph node metastasis in submucosally invaded gastrointestinal cancer patients. We have established an orthotopic early rectal cancer xenograft model with spontaneous lymph node metastasis by implantation of green fluorescent protein (GFP)-labeled human colon cancer cells into the submucosal layer of the murine rectum. A solution containing telomerase-specific oncolytic adenovirus was injected into the peritumoral submucosal space, followed by excision of the primary rectal tumors mimicking the endoscopic submucosal dissection (ESD) technique. Seven days after treatment, GFP signals had completely disappeared indicating that sentinel lymph node metastasis was selectively eradicated. Moreover, biologically treated mice were confirmed to be relapse-free even 4 weeks after treatment. These results indicate that virus-mediated biological ablation selectively targets lymph node metastasis and provides a potential alternative to surgery for submucosal invasive gastrointestinal cancer patients.</p>
</abstract>
</article-meta>
</front>
</pmc>
<affiliations>
<list>
<country>
<li>Japon</li>
<li>États-Unis</li>
</country>
</list>
<tree>
<country name="Japon">
<noRegion>
<name sortKey="Kikuchi, Satoru" sort="Kikuchi, Satoru" uniqKey="Kikuchi S" first="Satoru" last="Kikuchi">Satoru Kikuchi</name>
</noRegion>
<name sortKey="Fujiwara, Toshiyoshi" sort="Fujiwara, Toshiyoshi" uniqKey="Fujiwara T" first="Toshiyoshi" last="Fujiwara">Toshiyoshi Fujiwara</name>
<name sortKey="Hashimoto, Yuuri" sort="Hashimoto, Yuuri" uniqKey="Hashimoto Y" first="Yuuri" last="Hashimoto">Yuuri Hashimoto</name>
<name sortKey="Kagawa, Shunsuke" sort="Kagawa, Shunsuke" uniqKey="Kagawa S" first="Shunsuke" last="Kagawa">Shunsuke Kagawa</name>
<name sortKey="Kishimoto, Hiroyuki" sort="Kishimoto, Hiroyuki" uniqKey="Kishimoto H" first="Hiroyuki" last="Kishimoto">Hiroyuki Kishimoto</name>
<name sortKey="Kuroda, Shinji" sort="Kuroda, Shinji" uniqKey="Kuroda S" first="Shinji" last="Kuroda">Shinji Kuroda</name>
<name sortKey="Nagasaka, Takeshi" sort="Nagasaka, Takeshi" uniqKey="Nagasaka T" first="Takeshi" last="Nagasaka">Takeshi Nagasaka</name>
<name sortKey="Nishizaki, Masahiko" sort="Nishizaki, Masahiko" uniqKey="Nishizaki M" first="Masahiko" last="Nishizaki">Masahiko Nishizaki</name>
<name sortKey="Shirakawa, Yasuhiro" sort="Shirakawa, Yasuhiro" uniqKey="Shirakawa Y" first="Yasuhiro" last="Shirakawa">Yasuhiro Shirakawa</name>
<name sortKey="Tazawa, Hiroshi" sort="Tazawa, Hiroshi" uniqKey="Tazawa H" first="Hiroshi" last="Tazawa">Hiroshi Tazawa</name>
<name sortKey="Tazawa, Hiroshi" sort="Tazawa, Hiroshi" uniqKey="Tazawa H" first="Hiroshi" last="Tazawa">Hiroshi Tazawa</name>
<name sortKey="Urata, Yasuo" sort="Urata, Yasuo" uniqKey="Urata Y" first="Yasuo" last="Urata">Yasuo Urata</name>
</country>
<country name="États-Unis">
<noRegion>
<name sortKey="Hoffman, Robert M" sort="Hoffman, Robert M" uniqKey="Hoffman R" first="Robert M" last="Hoffman">Robert M. Hoffman</name>
</noRegion>
<name sortKey="Hoffman, Robert M" sort="Hoffman, Robert M" uniqKey="Hoffman R" first="Robert M" last="Hoffman">Robert M. Hoffman</name>
</country>
</tree>
</affiliations>
</record>

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