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PMID: 12069837 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Review

Mitogenic action of LPA in prostate.

Biochimica et biophysica acta ·Vol. 1582 ·No. 1-3 ·2002-05-23 ·Pages 265-9

Daaka Y

Abstract

The lipid growth factor lysophosphatidic acid (LPA) elicits multiple cellular responses, including cell growth and survival. LPA acts upon target cells by activating its cognate receptors, which belong to the G protein-coupled endothelial differentiation gene (EDG) family. To date, three known LPA receptors, termed LPA1, LPA2 and LPA3, have been molecularly characterized and cloned. Here, we review recent data describing the molecular steps involved in the LPA receptor-mediated activation of mitogenic extracellular signal-regulated kinase (ERK) pathway in prostate cancer. Induction of ERK by LPA proceeds via Gbetagamma-dependent activation of tyrosine kinases, including the epidermal growth factor (EGF) receptor and c-Src. Further, LPA-induced ERK activation involves matrix metalloproteinases (MMPs), which cause the release of active EGFR ligands. Finally, we present data demonstrating a correlation between the mitogenic effects of LPA and expression of the lp(A1) gene in the prostate cancer cells.

MeSH Terms
Animals Growth Substances/physiology Humans Lysophospholipids/physiology MAP Kinase Signaling System/physiology Male Mitogen-Activated Protein Kinases/metabolism Prostate/cytology,physiology
Chemicals
Growth Substances Lysophospholipids Mitogen-Activated Protein Kinases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Daaka Yehia
Department of Surgery, Duke University Medical Center, DUMC 2607, Durham, NC 27710, USA. daaka001@duke.edu
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
2002-05-23
Pages
265-9
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
Grants
NIA NIH HHS · R01 AG17952 · United States
NIDDK NIH HHS · R01 DK60917 · United States
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