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2014 Fiscal Year Final Research Report

Analysis of endometrial cancer stem cells

Research Project

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Project/Area Number 24592508
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Obstetrics and gynecology
Research InstitutionKanazawa University

Principal Investigator

NAKAMURA Mitsuhiro  金沢大学, 大学病院, 講師 (50377397)

Co-Investigator(Kenkyū-buntansha) KYO Satoru  島根大学, 医学部, 教授 (50272969)
Project Period (FY) 2012-04-01 – 2015-03-31
Keywords子宮内膜癌 / 癌幹細胞
Outline of Final Research Achievements

Previous our study demonstrated that CD133+ enodometrial cancer cells showed tumorigenic and self-renewal ability, suggesting that CD133 was a potential CSC marker in endometrial cancer. In this study, we focused on multilineage differentiation and investigated an ability of endothelial differentiation in endometrial CSCs. Immunohistochemistry of subcutaneous xenografts showed that human endometrial tumors contained human vessels labeled by human-specific anti-CD31 antibodies. Endothelial tube formation assay (in vitro angiogenesis) revealed that isolated CD133+ endometrial cancer cells could show tube formation while CD133- cells could not. CD133+ cells expressed VEGFR-1 higher than CD133- cells. Furthermore, in vitro angiogenesis assay demonstrated hypoxic condition could promote and keep tube formation in CD133+ cells, but not CD133- cells.

Free Research Field

婦人科腫瘍学

URL: 

Published: 2016-06-03  

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