Protein tyrosine phosphatase PTPRJ is negatively regulated by microRNA-328

Francesco Paduano1, Vincenzo Dattilo, Domenico Narciso

  • 1Dipartimento di Medicina Sperimentale e Clinica, Università Magna Graecia, Catanzaro, Italy. francesco.paduano@unicz.it

The FEBS Journal
|May 9, 2012
PubMed

Insights

MicroRNA-328 (miR-328) directly reduces PTPRJ expression in epithelial cells, promoting proliferation. Restoring PTPRJ negates miR-328

Area of Science:

  • Molecular Biology
  • Cancer Research
  • Genetics

Background:

  • Receptor-type protein tyrosine phosphatase PTPRJ expression is reduced in many human epithelial cancers.
  • The role of microRNAs (miRNAs) in regulating PTPRJ expression remains unexplored.

Purpose of the Study:

  • To investigate the role of microRNA-328 (miR-328) in regulating PTPRJ expression.
  • To determine the functional consequences of miR-328-mediated PTPRJ downregulation on epithelial cell proliferation.

Main Methods:

  • Overexpression of miR-328 in HeLa and SKBr3 cells.
  • Luciferase assay and site-specific mutagenesis to identify miRNA binding sites.
  • Small interfering RNA (siRNA) for PTPRJ knockdown and restoration.
  • Cell proliferation assays.

Main Results:

  • Overexpression of miR-328 significantly decreased PTPRJ expression in HeLa and SKBr3 cells.
  • miR-328 directly targets the 3'UTR of PTPRJ mRNA, reducing its levels.
  • miR-328 overexpression enhanced epithelial cell proliferation, mimicking PTPRJ downregulation.
  • The proliferative effect of miR-328 was dependent on PTPRJ levels.

Conclusions:

  • miR-328 directly downregulates PTPRJ expression by targeting its 3'UTR.
  • The interaction between miR-328 and PTPRJ contributes to increased epithelial cell proliferation.
  • This finding identifies a novel regulatory pathway with implications for cancer research.

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