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长链非编码RNA PTENP1在膀胱癌发生发展中的分子机制

余淦 欧正岳 陶启业 万国悦 陆宗浩 郎斌

南方医科大学学报2017,Vol.37Issue(11):1494-1500,7.
南方医科大学学报2017,Vol.37Issue(11):1494-1500,7.DOI:10.3969/j.issn.1673-4254.2017.11.11

长链非编码RNA PTENP1在膀胱癌发生发展中的分子机制

Role of lncRNA PTENP1 in tumorigenesis and progression of bladder cancer and the molecular mechanism

余淦 1欧正岳 2陶启业 2万国悦 2陆宗浩 2郎斌2

作者信息

  • 1. 华中科技大学同济医学院附属同济医院泌尿外科,湖北 武汉 430030
  • 2. 澳门理工学院高等卫生学校,澳门999078
  • 折叠

摘要

Abstract

Objective To explore the molecular mechanism underlying the biological function of lncRNA PTENP1 in bladder cancer. Methods Expressions of PTENP1, PTEN and miR-17 were examined by quantitative reverse transcriptase PCR (qRT-PCR) in 12 bladder cancer tissues. The expression of PTEN was examined by Western blotting in bladder cancer cell lines T24 and 5637 overexpressing PTENP1. Luciferase reporter assay was performed to confirm the targeting of miR-17 to PTENP1 and PTEN. T24 and 5637 cell lines with stable overexpression of PTENP1 and mir-17 were used to investigate effect of PTNE and miR-17 on the function of PTENP1 in bladder cancer. Results The expression of miR-17 was up-regulated and PTENP1 and PTEN were down-regulated in bladder cancer tissues, where a positive correlation was found between PTENP1 and PTEN expressions and a negative correlation between PTENP1 and miR-17 (P<0.05). Overexpression of PTENP1 in bladder cancer cell lines T24 and 5637 obviously enhanced the expression of PTEN protein. miR-17 was found to target both PTENP1 and PTEN and promote the growth of bladder cancer. miR-17 could partially restore the tumor-suppressing activity of PTENP1 in bladder cancer. Conclusion By binding with miR-17, lncRNA PTENP1 functions as a PTEN competing endogenous RNA (ceRNA) to suppress the progression of bladder cancer.

关键词

膀胱癌/PTENP1/分子机制/PTEN/miR-17/竞争性内源RNA

Key words

bladder cancer/PTENP1/molecular mechanism/PTEN/miR-17/competing endogenous RNA

引用本文复制引用

余淦,欧正岳,陶启业,万国悦,陆宗浩,郎斌..长链非编码RNA PTENP1在膀胱癌发生发展中的分子机制[J].南方医科大学学报,2017,37(11):1494-1500,7.

基金项目

澳门理工学院科研项目(RP/ESS-03/2015) (RP/ESS-03/2015)

南方医科大学学报

OA北大核心CSCDCSTPCDMEDLINE

1673-4254

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