Affiliation
Professorial Surgical Unit, University of Dublin, Trinity College, The Trinity Centre for Health Sciences, Adelaide & Meath Hospital Inc. NCH, Tallaght, Dublin, Ireland.Issue Date
2009-06MeSH
Anti-Inflammatory Agents, Non-SteroidalCyclooxygenase 2
Dinoprostone
Humans
Neoplasms
Neovascularization, Physiologic
Up-Regulation
Vascular Endothelial Growth Factor A
Metadata
Show full item recordCitation
COX-2, VEGF and tumour angiogenesis. 2009, 7 (3):174-80 SurgeonJournal
The surgeon : journal of the Royal Colleges of Surgeons of Edinburgh and IrelandPubMed ID
19580182Abstract
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.Language
enISSN
1479-666XCollections
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