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The p38 pathway, a major pleiotropic cascade that transduces stress and metastatic signals in endothelial cells

Journal

ONCOTARGET
Volume 8, Issue 33, Pages 55684-55714

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.18264

Keywords

p38MAPK; endothelial cells; oxidative stress; cancer; endothelial dysfunction

Funding

  1. International Outgoing Fellowship, Marie Curie People Programme, the European Union's Seventh Framework Program FP7 (REA grant) [326512]
  2. La Ligue contre le Cancer (Comites Loire-Atlantique, Morbihan, Cotes d'Armor)
  3. Natural Sciences and Engineering Research Council of Canada
  4. Canadian Institutes of Health Research and the Cancer Research Society

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By gating the traffic of molecules and cells across the vessel wall, endothelial cells play a central role in regulating cardiovascular functions and systemic homeostasis and in modulating pathophysiological processes such as inflammation and immunity. Accordingly, the loss of endothelial cell integrity is associated with pathological disorders that include atherosclerosis and cancer. The p38 mitogen-activated protein kinase (MAPK) cascades are major signaling pathways that regulate several functions of endothelial cells in response to exogenous and endogenous stimuli including growth factors, stress and cytokines. The p38 MAPK family contains four isoforms p38 alpha, p38 beta, p38 gamma and p38d that are encoded by four different genes. They are all widely expressed although to different levels in almost all human tissues. p38 alpha/MAPK14, that is ubiquitously expressed is the prototype member of the family and is referred here as p38. It regulates the production of inflammatory mediators, and controls cell proliferation, differentiation, migration and survival. Its activation in endothelial cells leads to actin remodeling, angiogenesis, DNA damage response and thereby has major impact on cardiovascular homeostasis, and on cancer progression. In this manuscript, we review the biology of p38 in regulating endothelial functions especially in response to oxidative stress and during the metastatic process.

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