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miR-34a 调控癌蛋白 Stathmin-1 的表达并促进前列腺癌进展。

miR-34a Regulates Expression of the Stathmin-1 Oncoprotein and Prostate Cancer Progression.

机构信息

Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama.

Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, Alabama.

出版信息

Mol Cancer Res. 2018 Jul;16(7):1125-1137. doi: 10.1158/1541-7786.MCR-17-0230. Epub 2017 Oct 12.

Abstract

In aggressive prostate cancers, the oncoprotein STMN1 (also known as stathmin 1 and oncoprotein 18) is often overexpressed. STMN1 is involved in various cellular processes, including cell proliferation, motility, and tumor metastasis. Here, it was found that the expression of STMN1 RNA and protein is elevated in metastatic prostate cancers. Knockdown of STMN1 resulted in reduced proliferation and invasion of cells and tumor growth and metastasis Furthermore, miR-34a downregulated STMN1 by directly binding to its 3'-UTR. Overexpression of miR-34a in prostate cancer cells reduced proliferation and colony formation, suggesting that it is a tumor suppressor. The transcriptional corepressor C-terminal binding protein 1 (CtBP1) negatively regulated expression of miR-34a. Furthermore, gene expression profiling of STMN1-modulated prostate cancer cells revealed molecular alterations, including elevated expression of growth differentiation factor 15 (GDF15), which is involved in cancer progression and potentially in STMN1-mediated oncogenesis. Thus, in prostate cancer, CtBP1-regulated miR-34a modulates STMN1 expression and is involved in cancer progression through the CtBP1\miR-34a\STMN1\GDF15 axis. The CtBP1\miR-34a\STMN1\GDF15 axis is a potential therapeutic target for treatment of aggressive prostate cancer. .

摘要

在侵袭性前列腺癌中,癌蛋白 STMN1(也称为 stathmin 1 和癌蛋白 18)常常过表达。STMN1 参与多种细胞过程,包括细胞增殖、运动和肿瘤转移。在这里,发现转移性前列腺癌中 STMN1 RNA 和蛋白的表达水平升高。STMN1 的敲低导致细胞增殖和侵袭以及肿瘤生长和转移减少。此外,miR-34a 通过直接结合其 3'-UTR 来下调 STMN1 的表达。前列腺癌细胞中 miR-34a 的过表达可减少增殖和集落形成,表明其为肿瘤抑制因子。转录核心抑制因子 C 端结合蛋白 1(CtBP1)负调控 miR-34a 的表达。此外,STMN1 调节的前列腺癌细胞的基因表达谱分析揭示了分子改变,包括生长分化因子 15(GDF15)的表达升高,GDF15 参与癌症进展,并可能在 STMN1 介导的致癌作用中发挥作用。因此,在前列腺癌中,CtBP1 调节的 miR-34a 调节 STMN1 的表达,并通过 CtBP1\miR-34a\STMN1\GDF15 轴参与癌症进展。CtBP1\miR-34a\STMN1\GDF15 轴是治疗侵袭性前列腺癌的潜在治疗靶点。

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