Molecular Cancer Therapeutics
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Mol Cancer Ther. 2004;3:363-371
© 2004 American Association for Cancer Research

Minireview

Cytochrome P450 enzymes: Novel options for cancer therapeutics

Morag C. E. McFadyen1, William T. Melvin2 and Graeme I. Murray1

Departments of 1 Pathology and 2 Molecular and Cell Biology, University of Aberdeen, Aberdeen, United Kingdom

Requests for Reprints: Morag C. E. McFadyen, Department of Pathology, University of Aberdeen, Foresterhill, Aberdeen, AB25 2ZD, United Kingdom. Phone: 44-1224-553792; Fax: 44-1224-663002. E-mail: m.mcfadyen{at}abdn.ac.uk

The concept of overexpression of individual forms of cytochrome P450 enzymes in tumor cells is now becoming well recognized. Indeed, a growing body of research highlights the overexpression of P450s, particularly CYP1B1, in tumor cells as representing novel targets for anticancer therapy. The purpose of this review is to outline the novel therapeutic options and opportunities arising from both enhanced endogenous expression of cytochrome P450 in tumors and cytochrome P450-mediated gene therapy.


Grant support: Cancer Research UK, Gray Fund, Chief Scientist Office Scottish Executive Health Department, Grampian University Hospital Trust, Knowledge Transfer Partnership, Tenovus-Scotland and University of Aberdeen Trust.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

3 KuDOS Pharmaceuticals Web site provides detailed information in the current status of AQ4N (http://www.kudospharma.co.uk/r_d/aq4n.php; accessed September 9, 2003).

Received 9/10/03; revised 11/ 7/03; accepted 12/15/03.







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Copyright © 2004 by the American Association for Cancer Research.