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2016 Fiscal Year Final Research Report

The mechanisms of autophagic cell death induction by histone deacetylase inhibitor SAHA

Research Project

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Project/Area Number 25462338
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Orthopaedic surgery
Research InstitutionKyushu University

Principal Investigator

Okada Takamitsu  九州大学, 大学病院, 助教 (70525550)

Project Period (FY) 2013-04-01 – 2017-03-31
Keywordsヒストン脱アセチル化酵素阻害剤 / オートファジー細胞死 / 多剤耐性骨肉腫細胞株
Outline of Final Research Achievements

There was no correlation between the expression of autophagy-related protein and acetylation of the histone. I was able to confirm that quantity of population of G2/M increased by SAHA. However, there was no correlation between G2/M introduction time and LC3-2 expression increasing time. SAHA induced the formation of autophagosome in a cell. I observed the period of the formation of autophagosome , there was no tendency of this period. I tried the making of the multidrug-resistant osteosarcoma cell animal model using osteosarcoma cell line: Saos2, but this cell line died the concentration of 25 ng/ml Dox. We could not make the multidrug-resistant Saos2 cell line.

Free Research Field

整形外科

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Published: 2018-03-22  

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