标题:miR-511 and miR-1297 Inhibit Human Lung Adenocarcinoma Cell Proliferation by Targeting Oncogene TRIB2
作者:Zhang, Chao; Chi, Yong Liang; Wang, Ping Yu; Wang, Ya Qi; Zhang, Yan Xia; Deng, Jingti; Lv, Chang Jun; Xie, Shu Yang
作者机构:[Lv, Chang Jun; Xie, Shu Yang] Binzhou Med Univ, Affiliated Hosp, Binzhou, Peoples R China.; [Zhang, Chao; Wang, Ping Yu; Wang, Ya Qi; Zhang, Yan Xi 更多
通讯作者:Lv, CJ
通讯作者地址:[Lv, CJ]Binzhou Med Univ, Affiliated Hosp, Binzhou, Peoples R China.
来源:PLOS ONE
出版年:2012
卷:7
期:10
DOI:10.1371/journal.pone.0046090
摘要:microRNAs (miRNAs) are small noncoding RNAs that regulate genes and contribute to many kinds of human diseases, including cancer. Two miRNAs, miR-511 and miR-1297, were investigated for a possible role in adenocarcinoma based on predicted binding sites for the TRIB2 oncogene by microRNA analysis software, and the pcDNA-GFP-TRIB2-3'UTR vector was constructed to investigate the interaction between TRIB2 and miR-511/1297 in the adenocarcinoma cell line A549. Green fluorescent protein (GFP) expression was estimated by fluorescence microscopy and flow cytometry after A549 cells were co-transfected with miR-511 (or miR-1297) and pcDNA-GFP-TRIB2-3'UTR vector. The expression of GFP in the miR-511- and miR-1297-treated cells was significantly downregulated in contrast with the negative-control (NC) miRNA-treated cells. The decreased expression of TRIB2 was further detected after miR-511 (or miR-1297) treatment by western blotting. The MTT test showed inhibition of A549 cell proliferation and Annexin V-FITC/PI dual staining showed increased apoptosis in the miR-511- and miR-1297-treated cells compared to the NC cultures. A transcription factor downstream of TRIB2, the CCAAT/enhancer-binding protein alpha (C/EBP alpha), was expression at higher levels after miR-511 (or miR-1297) decreasing TRIB2 expression. Our results illustrate that miR-511 and miR-1297 act as tumor suppressor genes, which could suppress A549 cell proliferation in vitro and in vivo by suppressing TRIB2 and further increasing C/EBP alpha expression.
收录类别:SCOPUS;SCIE
WOS核心被引频次:12
Scopus被引频次:47
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84867163639&doi=10.1371%2fjournal.pone.0046090&partnerID=40&md5=b0d89187c1efa2df4316330f845dfd58
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