miR-130a Deregulates PTEN and Stimulates Tumor Growth

Cancer Res. 2017 Nov 15;77(22):6168-6178. doi: 10.1158/0008-5472.CAN-17-0530. Epub 2017 Sep 21.

Abstract

H-RasV12 oncogene has been shown to promote autophagic cell death. Here, we provide evidence of a contextual role for H-RasV12 in cell death that is varied by its effects on miR-130a. In E1A-immortalized murine embryo fibroblasts, acute expression of H-RasV12 promoted apoptosis, but not autophagic cell death. miRNA screens in this system showed that miR-130a was strongly downregulated by H-RasV12 in this model system. Enforced expression of miR-130a increased cell proliferation in part via repression of PTEN. Consistent with this effect, miR-130a overexpression in human breast cancer cells promoted Akt phosphorylation, cell survival, and tumor growth. In clinical specimens of multiple human cancers, expression of miR-130 family members correlated inversely with PTEN expression. Overall, our results defined miR-130a as an oncogenic miRNA that targets PTEN to drive malignant cell survival and tumor growth. Cancer Res; 77(22); 6168-78. ©2017 AACR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Survival / genetics
  • Cells, Cultured
  • Embryo, Mammalian / cytology
  • Female
  • Fibroblasts / metabolism
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Neoplastic*
  • HEK293 Cells
  • Humans
  • MCF-7 Cells
  • Mice, Inbred BALB C
  • Mice, Nude
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Neoplasms / genetics*
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • PTEN Phosphohydrolase / genetics*
  • PTEN Phosphohydrolase / metabolism
  • Transplantation, Heterologous
  • ras Proteins / genetics

Substances

  • MIRN130 microRNA, human
  • MIRN130 microRNA, mouse
  • MicroRNAs
  • PTEN Phosphohydrolase
  • ras Proteins