COX-2, VEGF AND TUMOUR ANGIOGENESIS

被引:182
作者
Toomey, D. P. [1 ]
Murphy, J. F. [1 ]
Conlon, K. C. [1 ]
机构
[1] Univ Dublin, Adelaide& Meath Hosp Inc, NCH, Trinity Coll,Trinity Ctr Hlth Sci,Surg Unit, Dublin, Ireland
来源
SURGEON-JOURNAL OF THE ROYAL COLLEGES OF SURGEONS OF EDINBURGH AND IRELAND | 2009年 / 7卷 / 03期
关键词
COX-2; NON STEROIDAL ANTI-INFLAMMATORY DRUG; ANGIOGENESIS; VEGF; ENDOTHELIAL GROWTH-FACTOR; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; FAMILIAL ADENOMATOUS POLYPOSIS; PANCREATIC-CANCER CELLS; CYCLOOXYGENASE-2; EXPRESSION; COLORECTAL-CANCER; PROSTAGLANDIN E-2; PROSTACYCLIN SYNTHESIS; GASTRIC-CARCINOMA; THROMBOXANE A(2);
D O I
10.1016/S1479-666X(09)80042-5
中图分类号
R61 [外科手术学];
学科分类号
100210 [外科学];
摘要
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 turnout 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.
引用
收藏
页码:174 / 180
页数:7
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