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2017 Fiscal Year Final Research Report

Molecular dissection of Cancer microenvironment-related genes

Research Project

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Project/Area Number 15K08973
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Gastroenterology
Research InstitutionSapporo Medical University

Principal Investigator

YAMAMOTO Eiichiro  札幌医科大学, 医学部, 講師 (60567915)

Project Period (FY) 2015-04-01 – 2018-03-31
Keywords微小環境 / 大腸がん / 遺伝子発現
Outline of Final Research Achievements

We identified genes and splicing variant which were altered in the tumor endothelial cells. We then validated the results by RT-qPCR, and identified gene A as a novel candidate of the tumor endothelium-related gene. The Cancer Genome Atlas (TCGA) datasets revealed that higher expression of gene A is associated with worse overall survival of CRC patients. Knockdown of gene A in human umbilical vein endothelial cell (HUVEC) suppressed cell proliferation and in vitro tube formation. Injection of siRNA against gene A in mice transplanted with human CRC cells suppressed formation of microvessels in the xenografted tumors. Microarray analysis revealed that knockdown of gene A in HUVEC significantly affected gene expression signatures, including cell cycle regulation and interferon signaling. Our results suggest that gene A may play an important role in the angiogenesis in CRC, and that it could be a potential therapeutic target.

Free Research Field

消化器がん

URL: 

Published: 2019-03-29  

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