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MicroRNA-224靶向CNNM1抑制前列腺癌血管生成的实验研究

黄亚强 黄红星 麦智鹏 黎卫 郑轶群 袁润强

中国现代医学杂志2017,Vol.27Issue(17):19-24,6.
中国现代医学杂志2017,Vol.27Issue(17):19-24,6.DOI:10.3969/j.issn.1005-8982.2017.17.004

MicroRNA-224靶向CNNM1抑制前列腺癌血管生成的实验研究

miR-224 inhibits angiogenesis of prostate cancer by targeting cyclin protein M1

黄亚强 1黄红星 1麦智鹏 1黎卫 1郑轶群 1袁润强1

作者信息

  • 1. 中山大学附属中山医院 泌尿外科,广东 中山 528403
  • 折叠

摘要

Abstract

Objective To investigate the impacts of miR-224 on biochemical recurrence and angiogenesis of prostate cancer. Methods Bioinformatics analysis and luciferase reporter assay were performed to predict the gene that can be directly inhibited by miR-224. Taylor database was used for confirming the expressions of CNNM1 and miR-224, and their correlations with biochemical recurrence of prostate cancer. Finally, the impacts of CNNM1 and miR-224 on angiogenesis of prostate cancer were explored by PC3 cell in vitro and in vivo. Results CNNM1 was directly regulated by miR-224, and their expression levels were negatively correlated in prostate cancer tissue ( r=-0.378, P<0.05). miR-224 was negatively correlated to, while CNNM1 was positively correlated to biochemical recurrence of prostate cancer (P<0.05). The expressions of CNNM1 and CD31 decreased in the PC3 cells overexpressing miR-224 (P<0.05). However, CNNM1 enhanced the expression level of CD31 (P<0.05). The immunochemical staining of the transplantation tumor in the nude mice displayed that miR-224 overexpression could suppress angiogenesis in the prostate cancer tissue. Conclusions miR-224 suppresses angiogenesis and biochemical recurrence of prostate cancer by targeting CNNM1.

关键词

前列腺癌/microRNA-224/细胞周期调节蛋白1/生化复发/血管生成

Key words

prostate cancer/miR-224/CNNM1/biochemical recurrence/angiogenesis

分类

医药卫生

引用本文复制引用

黄亚强,黄红星,麦智鹏,黎卫,郑轶群,袁润强..MicroRNA-224靶向CNNM1抑制前列腺癌血管生成的实验研究[J].中国现代医学杂志,2017,27(17):19-24,6.

基金项目

中国博士后科学基金(No:2016M590842) (No:2016M590842)

广东省医学科研基金(No:A2016052) (No:A2016052)

广东省中山市科技计划(No:2016B1028) (No:2016B1028)

中国现代医学杂志

OACSTPCD

1005-8982

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