2015 Fiscal Year Final Research Report
Sox2 is a novel target gene for the treatment of lung squamous cell carcinoma.
Project/Area Number |
25462188
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Respiratory surgery
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Research Institution | Kawasaki Medical School |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
NAOMOTO YOSHIO 川崎医科大学, 医学部, 教授 (00237190)
YAMATSUJI TOMOKI 川崎医科大学, 医学部, 准教授 (40379730)
TAKAOKA MUNENORI 川崎医科大学, 医学部, 講師 (50548568)
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Keywords | 肺扁平上皮癌 |
Outline of Final Research Achievements |
Sox2 is a pluripotency controller that was recently identified as a novel oncogene, recurrently activated in lung squamous cell carcinoma (SCC). Inhibition of Sox2 by siRNA suppresses cell viability and colony formation of Sox2 expressing EBC2 and LK2 lung SCC cells. Moreover, Sox2 siRNA inhibits lung SCC growth in vivo in a xenograft mouse model derived from these cells. Cell cycle analysis showed that Sox2 silencing significantly increased the G1 population in the cells. We used biological studies to demonstrate that CDKN1A was suppressed by Sox2 in lung SCC cells. G1 cell cycle arrest induced by Sox2 siRNA was rescued by CDKN1A siRNA. These results indicate that targeting Sox2 is an effective strategy for the treatment of Sox2-expressing lung SCC and the tumorigenic effect of Sox2 in lung SCC cells is mediated in part by suppression of CDKN1A.
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Free Research Field |
医歯薬学
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