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British Journal of Cancer (2006) 94, 346–350. doi:10.1038/sj.bjc.6602942 www.bjcancer.com
Published online 17 January 2006

COX inhibitors and breast cancer

D Mazhar1, R Ang1 and J Waxman1

1Department of Cancer Medicine, Division of Medicine, Faculty of Medicine, Imperial College London, Room 1014 Garry Weston Centre, Hammersmith Campus, Du Cane Road, London W12 0NN, UK

Correspondence: Professor J Waxman, E-mail: j.waxman@imperial.ac.uk

Received 3 October 2005; Revised 6 December 2005; Accepted 6 December 2005; Published online 17 January 2006.

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Abstract

There is considerable evidence to suggest that prostaglandins play an important role in the development and growth of cancer. The enzyme cyclo-oxygenase (COX) catalyses the conversion of arachidonic acid to prostaglandins. In recent years, there has been interest in a possible role for COX inhibitors in the prevention and treatment of malignancy. Cyclo-oxygenase-2 (COX-2) is overexpressed in several epithelial tumours, including breast cancer. Preclinical evidence favours an antitumour role for COX inhibitors in breast cancer. However, the epidemiological evidence for an association is conflicting. Trials are being conducted to study the use of COX inhibitors alone and in combination with other agents in the chemoprevention of breast cancer, and in the neo-adjuvant, adjuvant, and metastatic treatment settings. In evaluating the potential use of these agents particularly in cancer chemoprophylaxis, the safety profile is as important as their efficacy. Concern over the cardiovascular safety of both selective and nonselective COX-inhibitors has recently been highlighted.

Keywords:

cyclo-oxygenase (COX), prostaglandin, breast cancer, NSAIDS, selective COX-2 inhibitor

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