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WISP-1 promotes VEGF-C-dependent lymphangiogenesis by inhibiting miR-300 in human oral squamous cell carcinoma cells

Identifieur interne : 000928 ( Main/Exploration ); précédent : 000927; suivant : 000929

WISP-1 promotes VEGF-C-dependent lymphangiogenesis by inhibiting miR-300 in human oral squamous cell carcinoma cells

Auteurs : Ching-Chia Lin [Taïwan] ; Po-Chun Chen [Taïwan] ; Ming-Yu Lein [Taïwan] ; Ching-Wen Tsao [Taïwan] ; Chiu-Chen Huang [Taïwan] ; Shih-Wei Wang [Taïwan] ; Chih-Hsin Tang [Taïwan] ; Kwong-Chung Tung [Taïwan]

Source :

RBID : PMC:4891098

Abstract

Oral squamous cell carcinoma (OSCC), which accounts for nearly 90% of head and neck cancers, is characterized by a poor prognosis and a low survival rate. Vascular endothelial growth factor-C (VEGF-C) has been implicated in lymphangiogenesis and is correlated with cancer metastasis. WNT1-inducible signaling pathway protein-1 (WISP)-1/CCN4 is an extracellular matrix-related protein that belongs to the CCN family and stimulates many biological functions. Our previous studies showed that WISP-1 plays an important role in OSCC migration and angiogenesis. However, the effect of WISP-1 on VEGF-C regulation and lymphangiogenesis in OSCC is poorly understood. Here, we showed a correlation between WISP-1 and VEGF-C in tissue specimens from patients with OSCC. To examine the lymphangiogenic effect of WISP-1, we used human lymphatic endothelial cells (LECs) to mimic lymphatic vessel formation. The results showed that conditioned media from WISP-1-treated OSCC cells promoted tube formation and cell migration in LECs. We also found that WISP-1-induced VEGF-C is mediated via the integrin αvβ3/integrin-linked kinase (ILK)/Akt signaling pathway. In addition, the expression of microRNA-300 (miR-300) was inhibited by WISP-1 via the integrin αvβ3/ILK/Akt cascade. Collectively, these results reveal the detailed mechanism by which WISP-1 promotes lymphangiogenesis via upregulation of VEGF-C expression in OSCC. Therefore, WISP-1 could serve as therapeutic target to prevent metastasis and lymphangiogenesis in OSCC.


Url:
DOI: 10.18632/oncotarget.7014
PubMed: 26824419
PubMed Central: 4891098


Affiliations:


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Le document en format XML

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<p>Oral squamous cell carcinoma (OSCC), which accounts for nearly 90% of head and neck cancers, is characterized by a poor prognosis and a low survival rate. Vascular endothelial growth factor-C (VEGF-C) has been implicated in lymphangiogenesis and is correlated with cancer metastasis. WNT1-inducible signaling pathway protein-1 (WISP)-1/CCN4 is an extracellular matrix-related protein that belongs to the CCN family and stimulates many biological functions. Our previous studies showed that WISP-1 plays an important role in OSCC migration and angiogenesis. However, the effect of WISP-1 on VEGF-C regulation and lymphangiogenesis in OSCC is poorly understood. Here, we showed a correlation between WISP-1 and VEGF-C in tissue specimens from patients with OSCC. To examine the lymphangiogenic effect of WISP-1, we used human lymphatic endothelial cells (LECs) to mimic lymphatic vessel formation. The results showed that conditioned media from WISP-1-treated OSCC cells promoted tube formation and cell migration in LECs. We also found that WISP-1-induced VEGF-C is mediated via the integrin αvβ3/integrin-linked kinase (ILK)/Akt signaling pathway. In addition, the expression of microRNA-300 (miR-300) was inhibited by WISP-1 via the integrin αvβ3/ILK/Akt cascade. Collectively, these results reveal the detailed mechanism by which WISP-1 promotes lymphangiogenesis via upregulation of VEGF-C expression in OSCC. Therefore, WISP-1 could serve as therapeutic target to prevent metastasis and lymphangiogenesis in OSCC.</p>
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<name sortKey="Lai, Ch" uniqKey="Lai C">CH Lai</name>
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<author>
<name sortKey="Tang, Ch" uniqKey="Tang C">CH Tang</name>
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<analytic>
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<name sortKey="Ambros, V" uniqKey="Ambros V">V Ambros</name>
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<analytic>
<author>
<name sortKey="Esquela Kerscher, A" uniqKey="Esquela Kerscher A">A Esquela-Kerscher</name>
</author>
<author>
<name sortKey="Slack, Fj" uniqKey="Slack F">FJ Slack</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Zhang Quan, Jk T" uniqKey="Zhang Quan J">JK-T Zhang Quan</name>
</author>
</analytic>
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<biblStruct>
<analytic>
<author>
<name sortKey="Yu, J" uniqKey="Yu J">J Yu</name>
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<author>
<name sortKey="Xie, F" uniqKey="Xie F">F Xie</name>
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<author>
<name sortKey="Chen, W" uniqKey="Chen W">W Chen</name>
</author>
<author>
<name sortKey="Xu, Q" uniqKey="Xu Q">Q Xu</name>
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</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Zhang, D" uniqKey="Zhang D">D Zhang</name>
</author>
<author>
<name sortKey="Yang, G" uniqKey="Yang G">G Yang</name>
</author>
<author>
<name sortKey="Chen, X" uniqKey="Chen X">X Chen</name>
</author>
<author>
<name sortKey="Li, C" uniqKey="Li C">C Li</name>
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<name sortKey="Wang, L" uniqKey="Wang L">L Wang</name>
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<author>
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<name sortKey="Zhang, W" uniqKey="Zhang W">W Zhang</name>
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<author>
<name sortKey="Han, Z" uniqKey="Han Z">Z Han</name>
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<author>
<name sortKey="Zhao, S" uniqKey="Zhao S">S Zhao</name>
</author>
</analytic>
</biblStruct>
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<name sortKey="Shu Chun Hsu, J Hl" uniqKey="Shu Chun Hsu J">J-HL Shu-Chun Hsu</name>
</author>
<author>
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<biblStruct>
<analytic>
<author>
<name sortKey="Huang, Cy" uniqKey="Huang C">CY Huang</name>
</author>
<author>
<name sortKey="Chen, Sy" uniqKey="Chen S">SY Chen</name>
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</biblStruct>
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</back>
</TEI>
<affiliations>
<list>
<country>
<li>Taïwan</li>
</country>
</list>
<tree>
<country name="Taïwan">
<noRegion>
<name sortKey="Lin, Ching Chia" sort="Lin, Ching Chia" uniqKey="Lin C" first="Ching-Chia" last="Lin">Ching-Chia Lin</name>
</noRegion>
<name sortKey="Chen, Po Chun" sort="Chen, Po Chun" uniqKey="Chen P" first="Po-Chun" last="Chen">Po-Chun Chen</name>
<name sortKey="Chen, Po Chun" sort="Chen, Po Chun" uniqKey="Chen P" first="Po-Chun" last="Chen">Po-Chun Chen</name>
<name sortKey="Huang, Chiu Chen" sort="Huang, Chiu Chen" uniqKey="Huang C" first="Chiu-Chen" last="Huang">Chiu-Chen Huang</name>
<name sortKey="Lein, Ming Yu" sort="Lein, Ming Yu" uniqKey="Lein M" first="Ming-Yu" last="Lein">Ming-Yu Lein</name>
<name sortKey="Lein, Ming Yu" sort="Lein, Ming Yu" uniqKey="Lein M" first="Ming-Yu" last="Lein">Ming-Yu Lein</name>
<name sortKey="Tang, Chih Hsin" sort="Tang, Chih Hsin" uniqKey="Tang C" first="Chih-Hsin" last="Tang">Chih-Hsin Tang</name>
<name sortKey="Tang, Chih Hsin" sort="Tang, Chih Hsin" uniqKey="Tang C" first="Chih-Hsin" last="Tang">Chih-Hsin Tang</name>
<name sortKey="Tang, Chih Hsin" sort="Tang, Chih Hsin" uniqKey="Tang C" first="Chih-Hsin" last="Tang">Chih-Hsin Tang</name>
<name sortKey="Tsao, Ching Wen" sort="Tsao, Ching Wen" uniqKey="Tsao C" first="Ching-Wen" last="Tsao">Ching-Wen Tsao</name>
<name sortKey="Tung, Kwong Chung" sort="Tung, Kwong Chung" uniqKey="Tung K" first="Kwong-Chung" last="Tung">Kwong-Chung Tung</name>
<name sortKey="Wang, Shih Wei" sort="Wang, Shih Wei" uniqKey="Wang S" first="Shih-Wei" last="Wang">Shih-Wei Wang</name>
</country>
</tree>
</affiliations>
</record>

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