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微小 RNA-18a 通过负向调控 PIAS3 来调节 STAT3 活性,从而参与胃腺癌的发生。

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

机构信息

Department of Molecular Pathology, Tokyo Medical University, 6-1-1 Shinjuku, Shinjuku-ku, Tokyo 160-8402, Japan.

出版信息

Br J Cancer. 2013 Feb 19;108(3):653-61. doi: 10.1038/bjc.2012.587. Epub 2013 Jan 15.

Abstract

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.

摘要

背景

MicroRNA(miRNA,miR)-18a 是 miR-17-92 簇的成员,miR-17-92 簇是一个重要的基因座,在几种癌症中显著过表达,与癌症的发生和发展有关。然而,miR-17-92 簇及其单个 miRNA 的作用机制在很大程度上尚不清楚。

方法和结果

在这项研究中,我们通过原位杂交(ISH)检测和拷贝数分析研究了胃组织微阵列(TMA)标本中 miR-17-92 簇的表达。我们发现 miR-18a 的表达水平高于簇中的其他五个 miRNA。此外,我们鉴定了信号转导和转录激活因子 3(STAT3)的直接靶蛋白抑制剂 3(PIAS3)作为胃癌中 miR-18a 的直接靶标。miR-18a 水平与 Survivin、Bcl-xL 和 c-Myc 的水平呈正相关,Survivin、Bcl-xL 和 c-Myc 是 STAT3 的下游转录靶标。PIAS3 可以负调控 STAT3 诱导的转录;与此一致的是,PIAS3 水平与 Survivin、Bcl-xL 和 c-Myc 的水平呈负相关。

结论

我们的研究结果表明,miR-18a 作为一种癌基因,在胃腺癌发生中起作用,至少部分通过负调控 PIAS3 从而调节 STAT3 靶基因的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4801/3593546/bd00d5807777/bjc2012587f1.jpg

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