miR-17-5p Promotes migration of human hepatocellular carcinoma cells through the p38 mitogen-activated protein kinase-heat shock protein 27 pathway

Hepatology. 2010 May;51(5):1614-23. doi: 10.1002/hep.23566.

Abstract

miR-17-5p is overexpressed in hepatocellular carcinoma (HCC), but the specific regulatory mechanisms of miR-17-5p in HCC remain unknown. We investigated the molecular basis of miR-17-5p as an oncogene in human HCC cell lines. Our in vivo and in vitro data indicate that miR-17-5p up-regulates the migration and proliferation of HCC cells. Interestingly, proteomic and western blotting assays revealed that miR-17-5p significantly activates the p38 mitogen-activated protein kinase MAPK pathway and increases the phosphorylation of heat shock protein 27 (HSP27). Our results also suggest that E2F1-dependent down-regulation of Wip1 regulates miR-17-5p-p38-HSP27 signaling. Furthermore, suppression of HSP27 expression by small interfering RNA or the p38 MAPK pathway-specific inhibitor SB203580 decreases the migration of HCC cells overexpressing miR-17-5p but does not reduce their proliferation. Finally, we show that miR-17-5p expression correlates well with HSP27 status in primary human HCC tissues with metastasis.

Conclusion: Our findings suggest that the p38 MAPK pathway plays a crucial role in miR-17-5p-induced phosphorylation of HSP27 and, as a consequence, phosphorylated HSP27 enhances the migration of HCC cells. Our data highlight an important role of miR-17-5p in the proliferation and migration of HCC cells and support the potential application of miR-17-5p in HCC therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Hepatocellular / metabolism
  • Carcinoma, Hepatocellular / pathology
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • E2F1 Transcription Factor / physiology
  • HSP27 Heat-Shock Proteins / biosynthesis
  • HSP27 Heat-Shock Proteins / physiology*
  • Humans
  • Imidazoles / pharmacology
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology
  • MicroRNAs / pharmacology*
  • Phosphoprotein Phosphatases / physiology
  • Protein Phosphatase 2C
  • Pyridines / pharmacology
  • RNA, Small Interfering / pharmacology
  • p38 Mitogen-Activated Protein Kinases / physiology*

Substances

  • E2F1 Transcription Factor
  • E2F1 protein, human
  • HSP27 Heat-Shock Proteins
  • Imidazoles
  • MIRN17 microRNA, human
  • MicroRNAs
  • Pyridines
  • RNA, Small Interfering
  • p38 Mitogen-Activated Protein Kinases
  • PPM1D protein, human
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 2C
  • SB 203580