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2014 Fiscal Year Final Research Report

Effect of CDK4/6 inhibitor in endometrial cancer

Research Project

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Project/Area Number 25893229
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Obstetrics and gynecology
Research InstitutionThe University of Tokyo (2014)
Saitama Medical University (2013)

Principal Investigator

IKEDA Yuji  東京大学, 医学部附属病院, 助教 (80713453)

Project Period (FY) 2013-08-30 – 2015-03-31
KeywordsCDK4/6 / 子宮体癌 / PI3K経路 / TP53 / 放射線治療
Outline of Final Research Achievements

The result of combination both CDK4/6 activity/expression and Ki67 expression was significantly correlated with the prognosis in patients with low risk endometrial cancer. However, the efficacy of CDK4/6 inhibitor to the endometrial cancer celllines was inferior to the other cancer types. Because not only CDK4/6 is suppressed by TP53 via p21, but also TP53 is related with apoptosis, we focused on TP53 and irradiation in endometrial cancer. Our result indicated mutation of TP53 could serve a biomarker to predict radioresistance, a dual PI3K/mTOR inhibitor sensitized cells to irradiation, and suppression of HIF1alpha, which was regulated at least in part by the PI3K/mTOR pathway, enhanced the cytotoxic effect of irradiation.

Free Research Field

婦人科癌

URL: 

Published: 2016-06-03  

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