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A FoxO1-Bim pathway is involved in HDAC inhibitor depsipeptide induced apoptosis
Yang Yang #,Ying Zhao,Jing Yang,Wei-guo Zhu *
Department of Biochemistry and Molecular Biology, Peking University Health Sciences Center
*Correspondence author
#Submitted by
Subject:
Funding: 教育部博士点基金,国家自然科学基金(No.20070001800 ,)
Opened online:17 March 2009
Accepted by: none
Citation: Yang Yang,Ying Zhao,Jing Yang.A FoxO1-Bim pathway is involved in HDAC inhibitor depsipeptide induced apoptosis[OL]. [17 March 2009] http://en.paper.edu.cn/en_releasepaper/content/30413
 
 
Histone deacetylase (HDAC) inhibitors have been shown to induce cell cycle arrest and apoptosis in cancer cells. However, the mechanisms of HDAC inhibitor induced apoptosis are not completely understood. In this study, a novel HDAC inhibitor, depsipeptide was found to induce p53-independent apoptosis in human lung cancer cells. Further study showed that Bim, a BH3-only pro-apoptotic protein, was significantly up-regulated by depsipeptide in cancer cells, indicating Bim may play a role in this depsipeptide induced apoptosis. In additional experiments, Bim’s function in depsipeptide-induced apoptosis was confirmed by knock down of Bim with RNAi. Furthermore, depsipeptide-induced expression of Bim was found to be dependent on forkhead transcription factor 1 (FoxO1) by FoxO1 siRNA. These data show for the first time that HDAC inhibitor may induce apoptosis through the FoxO1-Bim pathway.
Keywords:depsipeptide;;apoptosis;Bim;FoxO1
 
 
 

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