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微小RNA-139-5P通过靶向Notch1抑制人前列腺癌细胞增殖。

MicroRNA-139-5P inhibits human prostate cancer cell proliferation by targeting Notch1.

作者信息

Sun Qian, Weng Danhui, Li Kezhen, Li Shuang, Bai Xiangyang, Fang Can, Luo Danfeng, Wu Peng, Chen Gang, Wei Juncheng

机构信息

Cancer Biology Research Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430030, P.R. China.

出版信息

Oncol Lett. 2018 Jul;16(1):793-800. doi: 10.3892/ol.2018.8773. Epub 2018 May 22.

Abstract

Despite an improvement in the efficacy of chemotherapeutic agents, the outcome of patients with prostate cancer remains poor. MicroRNA (miRNA/miR)-139 expression is often downregulated in multiple types of tumor, including in prostate cancer. The aim of the present study was to investigate the inhibitory effect of miR-139 on the PC-3, C4-2B and LNCaP prostate cancer cell lines. Analysis of the cell cycle of PC-3, C4-2B and LNCaP cells transfected with miR-139 revealed a significantly increased percentage of cells in the G phase and a decreased percentage in the S and G phases compared with those transfected with a negative control miRNA. The growth inhibitory rate of miR-139-transfected cells 24, 48 and 72 h after transfection were 32.83±2.61, 52.58±3.2 and 62.36±4.55% in PC-3 cells; 30.28±2.25, 51.74±3.27 and 60.80±3.58% in C4-2B cells; and 33.20±2.67, 51.83±3.59 and 61.79±4.85% in LNCaP cells, respectively. The present study revealed that miR-139 inhibited the proliferation of prostate cancer cells by interfering with the cell cycle. Further study into the mechanism by which this happened suggested that miR-139 reduced cyclin D1 expression and inhibited cell proliferation through targeting Notch1.

摘要

尽管化疗药物的疗效有所提高,但前列腺癌患者的预后仍然很差。微小RNA(miRNA/miR)-139的表达在多种类型的肿瘤中,包括前列腺癌中,常常下调。本研究的目的是探讨miR-139对PC-3、C4-2B和LNCaP前列腺癌细胞系的抑制作用。对转染miR-139的PC-3、C4-2B和LNCaP细胞的细胞周期分析显示,与转染阴性对照miRNA的细胞相比,G期细胞百分比显著增加,S期和G期细胞百分比降低。转染miR-139的细胞在转染后24、48和72小时的生长抑制率在PC-3细胞中分别为32.83±2.61%、52.58±3.2%和62.36±4.55%;在C4-2B细胞中分别为30.28±2.25%、51.74±3.27%和60.80±3.58%;在LNCaP细胞中分别为33.20±2.67%、51.83±3.59%和61.79±4.85%。本研究表明,miR-139通过干扰细胞周期抑制前列腺癌细胞的增殖。对其发生机制的进一步研究表明,miR-139通过靶向Notch1降低细胞周期蛋白D1的表达并抑制细胞增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac8b/6019920/ab9b83811e7a/ol-16-01-0793-g00.jpg

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