Lentivirus mediated silencing of Ubiquitin Specific Peptidase 39 inhibits cell proliferation of human hepatocellular carcinoma cells in vitro (Publication with Expression of Concern)

被引:15
|
作者
Pan, Zeya [1 ]
Pan, Hao [2 ]
Zhang, Jin [1 ]
Yang, Yun [1 ]
Liu, Hui [1 ]
Yang, Yuan [1 ]
Huang, Gang [1 ]
Ni, Junsheng [1 ]
Huang, Jian [1 ]
Zhou, Weiping [1 ]
机构
[1] Second Mil Med Univ, Eastern Hepatobiliary Surg Hosp, Dept Hepat Surg 3, Shanghai 200438, Peoples R China
[2] Shanghai Municipal Ctr Dis Control & Prevent, Dept Infect Dis Control & Prevent, Shanghai 200336, Peoples R China
关键词
Ubiquitin Specific Peptidase 39; Lentivirus; Human hepatocellular carcinoma; Cell proliferation; Cell cycle; CANCER-CELLS; RNA INTERFERENCE; GENE-THERAPY; LIVER-CANCER; TRI-SNRNP; AURORA-B; PHASE-I; PROTEIN; YEAST; SPLICEOSOME;
D O I
10.1186/s40659-015-0006-y
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Ubiquitin Specific Peptidase 39 (USP39) is a 65 kDa SR-related protein involved in RNA splicing. Previous studies showed that USP39 is related with tumorigenesis of human breast cancer cells. Results: In the present study, we investigated the functions of USP39 in human hepatocellular carcinoma (HCC) cell line SMMC-7721. We knocked down the expression of USP39 through lentivirus mediated RNA interference. The results of qRT-PCR and western blotting assay showed that both the mRNA and protein levels were suppressed efficiently after USP39 specific shRNA was delivered into SMMC-7721 cells. Cell growth was significantly inhibited as determined by MTT assay. Crystal violet staining indicated that colony numbers and sizes were both reduced after knock-down of USP39. Furthermore, suppression of USP39 arrested cell cycle progression at G(2)/M phase in SMMC-7721cells. In addition, Annexin V showed that downregulation of USP39 significantly increased the population of apoptotic cells. Conclusions: All our results suggest that USP39 is important for HCC cell proliferation and is a potential target for molecular therapy of HCC.
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页数:7
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