2014 Fiscal Year Final Research Report
Development of complex treatment and clarification of the invasion and peritoneal dissemination mechanism of ovarian cancer which assumed epithelial mesenchymal transition a target
Project/Area Number |
25893093
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Research Category |
Grant-in-Aid for Research Activity Start-up
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Allocation Type | Single-year Grants |
Research Field |
Obstetrics and gynecology
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Research Institution | Nagoya University |
Principal Investigator |
SEKIYA RYUICHIRO 名古屋大学, 医学(系)研究科(研究院), 特任助教 (40712352)
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Project Period (FY) |
2013-08-30 – 2015-03-31
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Keywords | PLAGL2 / 卵巣癌 / RhoA / Rac1 |
Outline of Final Research Achievements |
Pleomorphic adenoma gene like-2 (PLAGL2), a member of the PLAG gene family, is a C2H2 zinc finger transcriptional factor that is involved in cellular transformation and apoptosis. We found that PLAGL2 depletion induced organization of stress fibers. In addition, formation of focal adhesions was promoted by PLAGL2 knockdown. Rac1 was inactivated in the absence of PLAGL2, whereas activity of RhoA was increased. Conversely, exogenous expression of PLAGL2 induced disruption of stress fiber formation and production of lamellipodia. Consistently, RhoA was suppressed and Rac1 was activated by PLAGL2 overexpression. PLAGL2 expression induced lamellipodia formation and disruption of stress fiber formation. Finally, we show that chimerin1(CHN1) expression is essential for Rac1 inactivation in PLAGL2-depleted cells.
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Free Research Field |
婦人科腫瘍学
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