RELATIONSHIP BETWEEN THE DEBRISOQUINE HYDROXYLASE POLYMORPHISM AND CANCER SUSCEPTIBILITY

被引:143
作者
WOLF, CR
SMITH, CAD
GOUGH, AC
MOSS, JE
VALLIS, KA
HOWARD, G
CAREY, FJ
MILLS, K
MCNEE, W
CARMICHAEL, J
SPURR, NK
机构
[1] IMPERIAL CANC RES FUND,CLARE HALL LABS,POTTERS BAR EN6 3LR,HERTS,ENGLAND
[2] UNIV EDINBURGH,WESTERN GEN HOSP,DEPT RADIOTHERAPY,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
[3] UNIV EDINBURGH,SCH MED,DEPT PATHOL,EDINBURGH EH8 9AG,MIDLOTHIAN,SCOTLAND
[4] GLASGOW ROYAL INFIRM,LEUKAEMIA RES FUND LABS,GLASGOW G4 0SF,SCOTLAND
[5] UNIV EDINBURGH,CITY HOSP,DEPT RESP MED,EDINBURGH EH10 5SB,MIDLOTHIAN,SCOTLAND
[6] CHURCHILL HOSP,IMPERIAL CANC RES FUND,OXFORD OX3 7LJ,ENGLAND
关键词
D O I
10.1093/carcin/13.6.1035
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
There have been a series of reports on the association of a genetic polymorphism at the cytochrome P450 CYP2D6 gene locus with cancer susceptibility. Many of these reports have remained contradictory either because of small numbers of patients studied or because of the limitations and controversy surrounding the pharmacokinetic assay used to identify affected individuals (poor metabolizers; PMs). We have recently developed a DNA-based assay that will allow the unequivocal identification of poor metabolizers and have applied this to the study of 1635 patients with different forms of cancer. Out of 361 lung cancer patients studied no statistically significant change in the proportion of PMs relative to controls was found. However, a significant increase in the proportion of poor metabolizers or heterozygotes was seen in leukaemia, bladder cancer and melanoma patients. This could be explained by a role for CYP2D6 in carcinogen detoxification or by linkage to another cancer-causing gene.
引用
收藏
页码:1035 / 1038
页数:4
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