Department of Urology, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Jingzhou City 434020, Hubei Province, P.R. China.
Department of Urology, Jingzhou Central Hospital, The Second Clinical Medical College, Yangtze University, Jingzhou City 434020, Hubei Province, P.R. China
Biosci Rep. 2019 Mar 28;39(3). doi: 10.1042/BSR20182097. Print 2019 Mar 29.
Long non-coding RNA (LncRNA) BRE-AS1 has recently proven to be a tumor suppressor in lung cancer. The present study aimed to investigate the involvement of lncRNA BRE-AS1 in prostate carcinoma (PC). In the present study we found that plasma BRE-AS1 and miR-145-5p were both down-regulated in PC patients than in healthy controls. Down-regulation of BRE-AS1 and miR-145-5p effectively distinguished early-stage PC patients from healthy controls. A significant and positive correlation between BRE-AS1 and miR-145-5p was only found in PC patients. BRE-AS1 overexpression mediated miR-145-5p up-regulation in PC cells, while miR-145-5p overexpression did not significantly affect BRE-AS1. Overexpression of BRE-AS1 and miR-145-5p led to inhibited proliferation and promoted apoptosis of PC cells. miR-145-5p inhibitor attenuated the effects of BRE-AS1 overexpression on cancer cell behaviors. Therefore, lncRNA BRE-AS1 may regulate cancer cell proliferation and apoptosis in PC by interacting with miR-145-5p.
长链非编码 RNA(lncRNA) BRE-AS1 最近被证明是肺癌的肿瘤抑制因子。本研究旨在探讨 lncRNA BRE-AS1 在前列腺癌(PC)中的作用。本研究发现,与健康对照组相比,PC 患者的血浆 BRE-AS1 和 miR-145-5p 均下调。下调 BRE-AS1 和 miR-145-5p 可有效区分早期 PC 患者与健康对照组。仅在 PC 患者中发现 BRE-AS1 和 miR-145-5p 之间存在显著正相关。BRE-AS1 过表达可介导 PC 细胞中 miR-145-5p 的上调,而 miR-145-5p 过表达对 BRE-AS1 无明显影响。BRE-AS1 和 miR-145-5p 的过表达导致 PC 细胞增殖受到抑制,凋亡增加。miR-145-5p 抑制剂减弱了 BRE-AS1 过表达对癌细胞行为的影响。因此,lncRNA BRE-AS1 可能通过与 miR-145-5p 相互作用来调节 PC 中癌细胞的增殖和凋亡。