Inactivation of oncogenic cAMP-specific phosphodiesterase 4D by miR-139-5p in response to p53 activation

Elife. 2016 Jul 7:5:e15978. doi: 10.7554/eLife.15978.

Abstract

Increasing evidence highlights the important roles of microRNAs in mediating p53's tumor suppression functions. Here, we report miR-139-5p as another new p53 microRNA target. p53 induced the transcription of miR-139-5p, which in turn suppressed the protein levels of phosphodiesterase 4D (PDE4D), an oncogenic protein involved in multiple tumor promoting processes. Knockdown of p53 reversed these effects. Also, overexpression of miR-139-5p decreased PDE4D levels and increased cellular cAMP levels, leading to BIM-mediated cell growth arrest. Furthermore, our analysis of human colorectal tumor specimens revealed significant inverse correlation between the expression of miR-139-5p and that of PDE4D. Finally, overexpression of miR-139-5p suppressed the growth of xenograft tumors, accompanied by decrease in PDE4D and increase in BIM. These results demonstrate that p53 inactivates oncogenic PDE4D by inducing the expression of miR-139-5p.

Keywords: BIM; PDE4D; apoptosis; cancer biology; human; miR-139-5p; mouse; p53; tumor suppression.

Publication types

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

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Colorectal Neoplasms / pathology
  • Cyclic Nucleotide Phosphodiesterases, Type 4 / biosynthesis*
  • Disease Models, Animal
  • Gene Expression Regulation, Neoplastic*
  • Heterografts
  • Humans
  • Mice, Inbred BALB C
  • MicroRNAs / metabolism*
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • MIRN139 microRNA, human
  • MicroRNAs
  • Tumor Suppressor Protein p53
  • Cyclic Nucleotide Phosphodiesterases, Type 4