MicroRNA-18a modulates STAT3 activity through negative regulation of PIAS3 during gastric adenocarcinogenesis

被引:86
作者
Wu, W. [1 ]
Takanashi, M. [1 ]
Bodigin, N. [1 ]
Ohno, S-i [1 ]
Fujita, K. [1 ]
Hoshino, S. [2 ]
Osaka, Y. [2 ]
Tsuchida, A. [2 ]
Kurode, M. [1 ,2 ]
机构
[1] Tokyo Med Univ, Dept Mol Pathol, Shinjuku Ku, Tokyo 1608402, Japan
[2] Tokyo Med Univ, Dept Surg 3, Shinjuku Ku, Tokyo 1608402, Japan
关键词
gastric adenocarcinoma; microRNA-18a; PIAS3; STAT3; Survivin; Bcl-xL; c-Myc; LUNG CANCERS; EXPRESSION; CLUSTER; CARCINOMA; APOPTOSIS; PROTEINS; CELLS; GENE; SUPPRESSORS; INHIBITION;
D O I
10.1038/bjc.2012.587
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: MicroRNA (miRNA, miR)-18a is a member of the miR-17-92 cluster, an important locus that is markedly overexpressed in several cancers and associated with cancer development and progression. However, the mechanism of action of the miR-17-92 cluster and its individual miRNAs are largely unknown. Methods and Results: In this study, we investigated the expression of the miR-17-92 cluster by in situ hybridisation (ISH) assay and copy-number analysis in gastric tissue microarray (TMA) specimens. We determined that miR-18a was present at higher levels than the other five miRNAs in the cluster. In addition, we identified Protein Inhibitor of Activated Signal Transducer and Activator of Transcription 3 (PIAS3) as a direct target of miR-18a in gastric cancer. miR-18a level was positively correlated with levels of Survivin, Bcl-xL, and c-Myc, which are downstream transcriptional targets of Signal Transducer and Activator of Transcription 3 (STAT3). STAT3-induced transcription can be negatively regulated by PIAS3; consistent with this, PIAS3 level was negatively correlated with levels of Survivin, Bcl-xL, and c-Myc. Conclusion: Our findings indicate that miR-18a acts as an oncogene and plays a role in gastric adenocarcinogenesis, at least in part by negatively regulating PIAS3 and thereby modulating expression of STAT3 target genes.
引用
收藏
页码:653 / 661
页数:9
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