TRIP6, as a target of miR-7, regulates the proliferation and metastasis of colorectal cancer cells

Biochem Biophys Res Commun. 2019 Jun 18;514(1):231-238. doi: 10.1016/j.bbrc.2019.04.092. Epub 2019 Apr 24.

Abstract

This study focuses on the role of miR-7 in colorectal cancer (CRC) cells by targeting thyroid receptor interactor protein 6 (TRIP6). Here, we report that miR-7 expression was down-regulated in colorectal cancer tissues and cell lines due to DNA hypermethylation. miR-7 overexpression significantly inhibits the proliferation and migration of CRC cells in vitro. TRIP6 was found to be a direct target gene of miR-7. The proliferation inhibition of CRC cells mediated by miR-7 could be rescued after TRIP6 overexpression in vitro and in vivo. Moreover, overexpression of TRIP6 reduced miR-7 inhibitor-mediated CRC cell migration and invasion. These findings demonstrate that miR-7 could inhibit the proliferation and migration of CRC cells by targeting TRIP6 and that miR-7 might serve as a good strategy for diagnosing and treating CRC.

Keywords: Colorectal cancer; Prognostic marker; TRIP6; Therapeutic target; miR-7.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions
  • Adaptor Proteins, Signal Transducing / genetics*
  • Adaptor Proteins, Signal Transducing / metabolism
  • Aged
  • Animals
  • Cell Line, Tumor
  • Cell Movement / genetics
  • Cell Proliferation / genetics
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / mortality
  • Colorectal Neoplasms / pathology*
  • DNA Methylation
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • LIM Domain Proteins / genetics*
  • LIM Domain Proteins / metabolism
  • Male
  • Mice, Nude
  • MicroRNAs / genetics*
  • Middle Aged
  • Survival Rate
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Xenograft Model Antitumor Assays

Substances

  • 3' Untranslated Regions
  • Adaptor Proteins, Signal Transducing
  • LIM Domain Proteins
  • MIRN7 microRNA, human
  • MicroRNAs
  • TRIP6 protein, human
  • Transcription Factors