Epstein-Barr virus miR-BART20-5p regulates cell proliferation and apoptosis by targeting BAD

被引:77
|
作者
Kim, Hyoji [1 ]
Choi, Hoyun [1 ]
Lee, Suk Kyeong [1 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Med Lifesci, Seoul 137701, South Korea
基金
新加坡国家研究基金会;
关键词
Epstein-Barr virus; BART miRNA; BAD; Cell proliferation; Apoptosis; GASTRIC-CARCINOMA CELLS; ENCODED MIR-BART20-5P; BH3-ONLY PROTEINS; MICRORNA TARGETS; EXPRESSION; CHEMORESISTANCE; INFECTION; GENES; RNA; REPLICATION;
D O I
10.1016/j.canlet.2014.10.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although Epstein Barr virus (EBV)BamHI A rightward transcript (BART) microRNAs (miRNAs) are ubiquitously expressed in EBV-associated tumors, the role of most BART miRNAs is unclear. In this study, we showed that Bcl-2-associated death promoter (BAD) expression was significantly lower in EBV-infected AGS-EBV cells than in EBV-negative AGS cells and investigated whether BART miRNAs target BAD. Using bioinformatics analysis, five BART miRNAs showing seed match with the 3' untranslated region (3'-UTR) of BAD were selected. Of these, only miR-BART20-5p reduced BAD expression when individually transfected into AGS cells. A luciferase assay revealed that miR-BART20-5p directly targets BAD. The expression of BAD mRNA and protein was decreased by miR-BART20-5p and increased by an inhibitor of miR-BART20-5p. PE Annexin V staining and cell proliferation assays showed that miR-BART20-5p reduced apoptosis and enhanced cell growth. Furthermore, miR-BART20-5p increased chemoresistance to 5-fluorouracil and docetaxel. Our data suggest that miR-BART20-5p contributes to tumorigenesis of EBV-associated gastric carcinoma by directly targeting the 3'-UTR of BAD. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:733 / 742
页数:10
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