articleHepatogastroenterologyOct 24, 2011Closed access

Hepatogastroenterology

Eastern Hepatobiliary Surgery Hospital · Second Military Medical University

PubMed
Indexed incrossrefpubmed

Abstract

Results

In the present study, LPA was found to increase HCC cell migration, invasion and adhesion. In addition, LPA increased MMP-9 expression level and induced activation of the p38 mitogen- activated protein kinase (MAPK) signaling. Furthermore, pharmacological inhibition of p38 MAPK signal pathway with SB203580 significantly attenuated LPA-induced HCC cell migration, invasion, and adhesion and abrogated LPA-induced MMP-9 expression and p38 MAPK phosphorylation.

Conclusions

We demonstrated a mechanism that LPA can activate p38 MAPK signaling, which is required for LPA-induced HCC cell migration, invasion, adhesion and MMP-9 expression, providing a novel biomarker and potential therapeutic target for HCC.

Citation impact

960
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Authors

5

Topics & keywords

Keywords
  • Lysophosphatidic acid
  • MAPK/ERK pathway
  • Cell migration
  • p38 mitogen-activated protein kinases
  • Cell biology
  • Cell adhesion
  • Focal adhesion
  • Signal transduction
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