实用医学杂志 ›› 2020, Vol. 36 ›› Issue (23): 3206-3210.doi: 10.3969/j.issn.1006⁃5725.2020.23.008

• 基础研究 • 上一篇    下一篇

lncRNA ZNF571⁃AS1对前列腺癌细胞增殖及侵袭能力的影响

杨凌博, 杨金辉, 鲁帅奇,李小辉, 卢绩   

  1. 1郑州大学附属洛阳中心医院泌尿外科(河南洛阳471009);2 吉林大学附属第一医院泌尿外科(长春130021)
  • 出版日期:2020-12-10 发布日期:2020-12-23
  • 通讯作者: 卢绩E⁃mail:orient0107@163.com
  • 基金资助:
    国家自然科学基金(编号:31501052)

Effects of lncRNA ZNF571 ⁃ AS1 on proliferation and invasion of prostate cancer cells

YANG Lingbo, YANG Jinhui,LU Shuaiqi,LI Xiaohui,LU Ji   

  1. Department of Urology,Luoyang Central Hospital Affiliated to Zhengzhou University,Luoyang 471009,China
  • Online:2020-12-10 Published:2020-12-23
  • Contact: LU Ji E⁃mail:orient0107@163.com

摘要:

目的 研究长链非编码RNA(long non⁃coding RNA,lncRNA)ZNF571⁃AS1在前列腺癌中的表达,探讨其对前列腺癌细胞增殖、侵袭能力的影响及分子机制。方法 采用实时定量聚合酶链反应(qPCR)技术检测ZNF571⁃AS1在前列腺癌组织及癌旁组织、前列腺癌细胞系及正常前列腺上皮细胞中的表达。以ZNF571⁃AS1表达最多的细胞系为研究,分别转染沉默ZNF571⁃AS1基因的质粒和阴性对照质粒。应用细胞增殖实验(MTT法)和小室(Transwell)实验检测ZNF571⁃AS1对前列腺癌细胞的增殖和侵袭的影响。生物信息学技术预测ZNF571⁃AS1的分子机制。qPCR和Western blot法分别检测下游靶基因的表达。结果 前列腺癌组织中ZNF571⁃AS1的表达显著高于癌旁组织(P<0.01)。前列腺癌细胞中ZNF571⁃AS1的表达显著高于正常前列腺上皮细胞(P<0.01),DU⁃145细胞中的表达最多(P<0.01)。低表达ZNF571⁃AS1可显著抑制DU⁃145细胞的增殖和侵袭能力(P<0.05)。ZNF571⁃AS1 的下游靶基因可能是miR⁃301b⁃3p,miR⁃301b⁃3p 的靶基因可能是雄激素受体。低表达ZNF571⁃AS1可显著上调DU⁃145细胞中miR⁃301b⁃3p的表达(P<0.01),抑制AR基因的表达(P<0.01)。结论 ZNF571⁃AS1在前列腺癌组织和细胞系中表达显著上调,ZNF571⁃AS1可能通过调控miR⁃301b⁃3p/AR信号通路影响前列腺癌DU⁃145细胞的增殖和侵袭能力。

关键词: 长链非编码RNA, 雄激素受体, 前列腺癌, 增殖, 侵袭

Abstract:

Objective To study the expression of long non⁃coding RNA(lncRNA)ZNF571⁃AS1 inprostate cancer,to clarify its effect on the proliferation and invasion of prostate cancer cells and its molecularmechanism. Methods Real⁃time quantitative polymerase chain reaction(qPCR)was used to detect the expres⁃sion of ZNF571⁃AS1 in prostate cancer tissues,adjacent tissues,prostate cancer cell lines and normal prostateepithelial cell. The cell line with the most expression of ZNF571⁃AS1 was used as a study. The plasmid thatsilenced the ZNF571⁃AS1 gene and the negative control plasmid were transfected separately. The effects of ZNF571⁃AS1 on the proliferation and invasion of prostate cancer cells were detected by cell proliferation experiment(MTTmethod)and Transwell experiment. Bioinformatics technology predicts the molecular mechanism of ZNF571⁃AS1.qPCR and Western blot methods were used to detect the expression of downstream target genes. Results Theexpression of ZNF571⁃AS1 in prostate cancer tissue was significantly higher than that in adjacent tissues(P < 0.01).The expression of ZNF571⁃AS1 in prostate cancer cells was significantly higher than that in normal prostate epithelialcells(P < 0.01),and the expression in DU⁃145 cells was the most(P < 0.01). Low expression of ZNF571⁃AS1can significantly inhibit the proliferation and invasion ability of DU⁃145 cells(P < 0.05). The downstream targetgene of ZNF571⁃AS1 may be miR⁃301b⁃3p,and the target gene of miR⁃301b⁃3p may be androgen receptor(AR).Low expression of ZNF571⁃AS1 can significantly up⁃regulate the expression of miR⁃301b⁃3p in DU⁃145 cells(P < 0.01),and inhibit the expression of AR gene(P < 0.01). Conclusion ZNF571⁃AS1 is significantly up⁃regulated in prostate cancer tissues and cell lines. ZNF571⁃AS1 may affect the proliferation and invasion of prostatecancer DU⁃145 cells by regulating the miR⁃301b⁃3p/AR signaling pathway.

Key words: long?chain non?coding RNA, androgen receptor, prostate cancer, proliferation, invasion