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miRNA-183-3p 通过下调高迁移率族核小体结合域 5 抑制人前列腺癌的进展。

microRNA-183-3p Inhibits Progression of Human Prostate Cancer by Downregulating High-Mobility Group Nucleosome Binding Domain 5.

机构信息

1Department of Urology, Peking University First Hospital, Institute of Urology, Peking University, National Urological Cancer Centre, Beijing, China.

2Department of Urology, Affiliated Hospital of Yangzhou University, Yangzhou University, Yangzhou, Jiangsu, China.

出版信息

DNA Cell Biol. 2019 Aug;38(8):840-848. doi: 10.1089/dna.2019.4642. Epub 2019 Jul 17.

DOI:10.1089/dna.2019.4642
PMID:31314587
Abstract

microRNAs are a class of noncoding RNAs that play important roles in cancer progression. microRNA-183-3p (miR-183-3p) is a novel microRNA that is dysregulated in many kinds of cancers. Our previous studies found high expression and oncologic role of high-mobility group nucleosome binding domain 5 () in prostate cancer. In this study, we found that miR-183-3p was downregulated in prostate cancer cells and primary tissues compared with normal controls. In addition, miR-183-3p expression was negatively correlated with expression. On the basis of bioinformatics predication and quantitative polymerase chain reaction and Western blot verification, it is demonstrated that miR-183-3p regulated expression. Luciferase reporter assay confirmed that miR-183-3p directly targeted the 3'-untranslated region of . Interestingly, cell proliferation and migration inhibition and apoptosis induction were also observed in miR-183-3p transfected human prostate cancer VCap and C4-2 cells. Moreover, overexpression of significantly reversed the inhibitory effect on cell proliferation and migration and promoted effect on cell apoptosis by miR-183-3p. Our data suggest that dysfunction of miR-183-3p- axis plays an oncogenic role and can be a therapeutic target for prostate cancer.

摘要

microRNAs 是一类在癌症进展中发挥重要作用的非编码 RNA。microRNA-183-3p(miR-183-3p)是一种新型的 microRNA,在许多类型的癌症中失调。我们之前的研究发现高迁移率族核小体结合域 5()在前列腺癌中的高表达和致癌作用。在这项研究中,我们发现与正常对照相比,前列腺癌细胞和原发性组织中的 miR-183-3p 表达下调。此外,miR-183-3p 的表达与的表达呈负相关。基于生物信息学预测和定量聚合酶链反应及 Western blot 验证,证明 miR-183-3p 调节的表达。荧光素酶报告基因检测证实 miR-183-3p 可直接靶向。有趣的是,在 miR-183-3p 转染的人前列腺癌细胞 VCap 和 C4-2 中观察到细胞增殖、迁移抑制和凋亡诱导。此外,过表达可显著逆转 miR-183-3p 对细胞增殖和迁移的抑制作用,并促进细胞凋亡。我们的数据表明,miR-183-3p-轴的功能障碍发挥致癌作用,可作为前列腺癌的治疗靶点。

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