学科主题基础医学
Knockdown of WWP1 inhibits growth and induces apoptosis in hepatoma carcinoma cells through the activation of caspase3 and p53
Cheng, Qian; Cao, Xiaoxiao; Yuan, Fuwen; Li, Guodong; Tong, Tanjun
关键词Wwp1 Hcc Growth Apoptosis Caspase3 P53
刊名BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
2014-06-06
DOI10.1016/j.bbrc.2014.04.117
448期:3页:248-254
收录类别SCI
文章类型Article
WOS标题词Science & Technology
类目[WOS]Biochemistry & Molecular Biology ; Biophysics
研究领域[WOS]Biochemistry & Molecular Biology ; Biophysics
关键词[WOS]UBIQUITIN E3 LIGASE ; HEPATOCELLULAR-CARCINOMA ; CELLULAR SENESCENCE ; PROTEIN ; TRANSCRIPTION ; DEGRADATION ; CANCER ; IDENTIFICATION ; TARGETS ; FAMILY
英文摘要

The activation of oncogenes and the loss of tumor suppressor genes are believed to play critical roles in the pathogenesis of human hepatocellular carcinoma (HCC). The human WW domain containing E3 ubiquitin protein ligase 1 (WWP1) gene is frequently amplified in prostate and breast cancers, however, its role in cancer has not yet been extensively studied. Especially, the role of WWP1 in HCC has not yet been studied. Firstly, we analyzed the expression of WWP1 in HCC samples. We found that protein levels of WWP1 are higher in most HCC cancerous tissues as compared with their matched adjacent non-tumor tissues. Additionally, the WWP1 mRNA was also amplified in all 7 HCC tissues. Knockdown of the endogenous WWP1 using small interfering RNA further showed that deficiency of WWP1 suppressed cell growth and caused apoptosis in HCC cells. Knocking down WWP1 promoted cleaved caspase3 protein and p53 expression in HCC cells, and caspase3 inhibition could prevent cell apoptosis induced by the knockdown of WWP1. All together these results indicate that protein levels of WWP1 in most HCC tissues are higher than non-tumor tissues, and knockdown of WWP1 inhibits growth and induces apoptosis in HCC cells through the activation of caspase3 and p53. Therefore, WWP1 gene might be a potential molecular target of HCC. (C) 2014 Elsevier Inc. All rights reserved.

语种英语
WOS记录号WOS:000337070800002
项目编号2013CB530801 ; 2012CB911293 ; 81372164
资助机构National Basic Research Programs of China ; National Nature Science Foundation of China
引用统计
被引频次:20[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.bjmu.edu.cn/handle/400002259/55439
专题北京大学基础医学院_北京大学衰老研究中心
北京大学基础医学院
作者单位Peking Univ, Hlth Sci Ctr, Res Ctr Aging, Dept Biochem & Mol Biol, Beijing 100191, Peoples R China
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GB/T 7714
Cheng, Qian,Cao, Xiaoxiao,Yuan, Fuwen,et al. Knockdown of WWP1 inhibits growth and induces apoptosis in hepatoma carcinoma cells through the activation of caspase3 and p53[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2014,448(3):248-254.
APA Cheng, Qian,Cao, Xiaoxiao,Yuan, Fuwen,Li, Guodong,&Tong, Tanjun.(2014).Knockdown of WWP1 inhibits growth and induces apoptosis in hepatoma carcinoma cells through the activation of caspase3 and p53.BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,448(3),248-254.
MLA Cheng, Qian,et al."Knockdown of WWP1 inhibits growth and induces apoptosis in hepatoma carcinoma cells through the activation of caspase3 and p53".BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 448.3(2014):248-254.
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