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2015 Fiscal Year Final Research Report

Analysis of molecular mechanisms involved in the susceptibility to statins on cancer cells

Research Project

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Project/Area Number 26890019
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Tumor diagnostics
Research InstitutionTottori University

Principal Investigator

Warita Katsuhiko  鳥取大学, 農学部, 准教授 (40452669)

Co-Investigator(Renkei-kenkyūsha) MIKI TAKANORI  香川大学, 医学部, 教授 (30274294)
HOSAKA YOSHINAO  鳥取大学, 農学部, 教授 (00337023)
OHTA KEN-ICHI  香川大学, 医学部, 助教 (50403720)
SUZUKI SHINGO  香川大学, 医学部, 助教 (50451430)
Research Collaborator WARITA TOMOKO (三觜 友子)  徳島文理大学, 薬学部, 研究員 (00753112)
Oltvai Zoltan N.  ピッツバーグ大学, 医学部, 准教授
Project Period (FY) 2014-08-29 – 2016-03-31
Keywords薬効評価と予測 / がん細胞の特性 / 化学療法 / スタチン系薬剤
Outline of Final Research Achievements

The anti-proliferative effect of stains on cancer cells has received widespread attention, since it has been reported that the statins may exhibit an anti-cancer effect in addition to their cholesterol-lowering effect. However, what type of cancer cell statin is effective for is unclear. Our previous study identified E-cadherin as a candidate factor determining the susceptibility to statin. To demonstrate that E-cadherin actually determines the susceptibility of cancer cells to statin, we examined if the regulation of E-cadherin expression has an influence on the susceptibility of cancer cells to statin in the present study. When E-cadherin gene (CDH1) was inserted into the statin-sensitive cells which had no E-cadherin, the half maximal inhibitory concentration (IC50) increased 3.7-fold. On the other hand, E-cadherin knockdown in the statin-resistant cancer cells increased their susceptibility to statin. These results strongly suggest that E-cadherin is a statin resistance factor.

Free Research Field

腫瘍生物学

URL: 

Published: 2017-05-10  

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