Pharmacogenetics and Genomics

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Pharmacogenetics and Genomics:
October 2005 - Volume 15 - Issue 10 - pp 713-721
Original Articles

No evidence that polymorphisms in CYP2C8, CYP2C9, UGT1A6, PPAR[delta] and PPAR[gamma] act as modifiers of the protective effect of regular NSAID use on the risk of colorectal carcinoma

McGreavey, Louise E.; Turner, Faye; Smith, Gillian; Boylan, Katherine; Timothy Bishop, D.; Forman, David; Roland Wolf, C.; Barrett, Jennifer H.; the Colorectal Cancer Study Group

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Abstract

Objectives: Regular continuous non-steroidal anti-inflammatory drug (NSAID) use has been associated with a reduction in risk of colorectal cancer. Our objective was to investigate whether or not a number of the polymorphic genes involved in the metabolism of NSAIDs, including cytochrome P450 s (CYPs), act as modifiers of this protective effect.

Methods: As part of a multi-centre case-control study, 478 colorectal cancer patients and 733 controls (433 matched case-control pairs) answered questions on NSAID use. These individuals were then genotyped for common polymorphisms in P450 CYP2C8, P450 CYP2C9, UDP-glucuronosyl transferase (UGT)1A6 and peroxisome proliferator-activated receptor isoforms δ and γ (PPARδ and PPARγ).

Results and conclusion: Our study confirmed the reduction in risk of colorectal cancer with regular NSAID use (odds ratio (OR)=0.73, 95% confidence interval (CI) (0.56, 0.95)) but showed that none of the polymorphic genes studied appeared to modify the protective effect of regular NSAID use.

© 2005 Lippincott Williams & Wilkins, Inc.

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