Enhanced proliferation of human hepatoma cells by PAR-2 agonists via the ERK/AP-1 pathway

Oncol Rep. 2012 Nov;28(5):1665-72. doi: 10.3892/or.2012.2007. Epub 2012 Aug 31.

Abstract

To investigate the expression and role of PAR-2 in the proliferation of the human hepatoma cell line HepG2, PAR-2 protein and mRNA expression were evaluated by immuno-histochemistry, immunofluorescence and RT-PCR analysis. The signaling pathways downstream of PAR-2 activation that lead to hepatoma cell proliferation were analyzed. The results showed that PAR-2 is expressed in human hepatoma cells and PAR-2 mRNA expression was found to be upregulated in cells treated with trypsin or SLIGKV-NH2 (P<0.001). The proliferation rate of HepG2 cells treated with trypsin or SLIGKV-NH2 was significantly increased (P<0.001). The percentage of S phase, G2/M phase and the proliferation index (PI) of HepG2 cells treated with trypsin or SLIGKV-NH2 were significantly elevated (P<0.001). The proliferative responses of HepG2 to trypsin and SLIGKV-NH2 were associated with the upregulation of c-fos and PCNA, which were significantly blocked by PD98059 pretreatment. In conclusion, our results indicate that PAR-2 enhances proliferation of human hepatoma cells possibly via the ERK/AP-1 pathway.

MeSH terms

  • Carcinoma, Hepatocellular / metabolism*
  • Carcinoma, Hepatocellular / pathology
  • Cell Cycle Checkpoints / drug effects
  • Cell Line, Tumor
  • Cell Proliferation
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Flavonoids / pharmacology
  • Hep G2 Cells
  • Humans
  • Liver Neoplasms / metabolism
  • Oligopeptides / pharmacology
  • Proliferating Cell Nuclear Antigen / biosynthesis
  • Proliferating Cell Nuclear Antigen / genetics
  • Proto-Oncogene Proteins c-fos / biosynthesis
  • Proto-Oncogene Proteins c-fos / genetics
  • RNA, Messenger / biosynthesis
  • Receptor, PAR-2 / agonists*
  • Receptor, PAR-2 / genetics
  • Receptor, PAR-2 / metabolism*
  • Signal Transduction / drug effects
  • Transcription Factor AP-1 / metabolism*
  • Trypsin / pharmacology

Substances

  • Flavonoids
  • Oligopeptides
  • Proliferating Cell Nuclear Antigen
  • Proto-Oncogene Proteins c-fos
  • RNA, Messenger
  • Receptor, PAR-2
  • Transcription Factor AP-1
  • seryl-leucyl-isoleucyl-glycyl-lysyl-valinamide
  • Extracellular Signal-Regulated MAP Kinases
  • Trypsin
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one