COX-2, VEGF and tumour angiogenesis

Epidemiological evidence suggests a protective effective of regular NSAID use against developing cancer. Cyclooxygenase-2, a target of NSAIDs, is upregulated in many cancers and has been associated with increased VEGF production and angiogenesis. Angiogenesis is the formation of new vessels from exi...

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Veröffentlicht in:The surgeon (Edinburgh) 2009-06, Vol.7 (3), p.174-180
Hauptverfasser: Toomey, D.P, Murphy, J.F, Conlon, K.C
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description Epidemiological evidence suggests a protective effective of regular NSAID use against developing cancer. Cyclooxygenase-2, a target of NSAIDs, is upregulated in many cancers and has been associated with increased VEGF production and angiogenesis. Angiogenesis is the formation of new vessels from existing vasculature and as an essential process for tumour development represents an important therapeutic target. Following an extensive review of the literature this article details the current knowledge on the role of COX-2 in tumorigenesis focusing on its relationship to angiogenesis and VEGF production by tumour cells. While COX-2 is clearly detrimental to prognosis and NSAIDs have a beneficial effect, the possibility of COX-2 independent effects being partly or wholly responsible for this benefit cannot be excluded.
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subjects angiogenesis
Anti-Inflammatory Agents, Non-Steroidal - pharmacology
COX-2
Cyclooxygenase 2 - physiology
Dinoprostone - physiology
Humans
Neoplasms - drug therapy
Neoplasms - physiopathology
Neovascularization, Physiologic - drug effects
Neovascularization, Physiologic - physiology
non steroidal anti-inflammatory drug
Surgery
Up-Regulation - physiology
Vascular Endothelial Growth Factor A - physiology
VEGF
title COX-2, VEGF and tumour angiogenesis
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