2010 Fiscal Year Final Research Report
Mechanism of cancer-selective cell death induced by increased genomic instability and application of the cell death mechanism to cancer therapy
Project/Area Number |
20590061
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Biological pharmacy
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Research Institution | Hiroshima University |
Principal Investigator |
SHIMAMOTO Akira Hiroshima University, 大学院・医歯薬学総合研究科, 准教授 (70432713)
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Co-Investigator(Kenkyū-buntansha) |
TAHARA Hidetoshi 広島大学, 大学院・医歯薬学総合研究科, 教授 (00271065)
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Project Period (FY) |
2008 – 2010
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Keywords | がん細胞選択的細胞死 / 分裂期細胞死 / スピンドルチェックポイント / ゲノム不安定性 / shRNAスクリーニング |
Research Abstract |
Spindle assembly checkpoint (SAC) can induce cancer-selective mitotic cell death. Although the cell death is induced after M-phase arrest by SAC activation, the mechanism behind mitotic cell death is unclear. In this study, I discovered candidate genes associated with mitotic cell death by shRNA screening. Further, seven genes were identified by using siRNAs that specifically suppress the candidate genes.
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[Journal Article] miR-22 represses cancer progression by inducing cellular senescence.2011
Author(s)
Dan Xu, Fumitaka Takeshita, Yumiko Hino, Saori Fukunaga, Yasusei Kudo, Aya Tamaki, Junko Matsunaga, Ryou-u Takahashi, Takashi Takata, Akira Shimamoto, Takahiro Ochiya, Hidetoshi Tahara
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Journal Title
Journal of Cell Biology 193 2
Pages: 409-424
Peer Reviewed
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