Association of CYP1B1 genetic polymorphism with incidence to breast and lung cancer

被引:149
作者
Watanabe, J [1 ]
Shimada, T
Gillam, EMJ
Ikuta, T
Suemasu, K
Higashi, Y
Gotoh, O
Kawajiri, K
机构
[1] Saitama Canc Ctr, Res Inst, Lab Canc Diag & Therapy, Ina, Saitama 3620806, Japan
[2] Saitama Canc Ctr, Saitama Canc Ctr Hosp, Dept Breast Surg Clin, Ina, Saitama 362, Japan
[3] Osaka Prefectural Inst Publ Hlth, Higashinari Ku, Osaka 537, Japan
[4] Univ Queensland, Dept Physiol & Pharmacol, St Lucia, Qld, Australia
来源
PHARMACOGENETICS | 2000年 / 10卷 / 01期
关键词
CYP1B1; genetic polymorphism; breast cancer; estradiol; 4-hydroxylase; lung cancer;
D O I
10.1097/00008571-200002000-00004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cytochrome P450 1B1 (CYP1B1) participates in the metabolic activation of a number of procarcinogens including benzo[a]pyrene and the hydroxylation of 17 beta-estradiol at the C-4 position, In this study, we investigated the association between CYP1B1 genetic polymorphism and breast or lung cancer incidence. The Ala-Ser polymorphism at codon 119 in presumed substrate recognition site 1 was significantly associated with the incidence of breast or squamous cell carcinoma of the lung, On the other hand, Leu-Val polymorphism at codon 432 did not show any association to the cancers. An allele containing both Ala and Leu simultaneously, comprised 75% of alleles among 315 Japanese healthy controls, was significantly inversely associated with breast cancer incidence. When expressed in a recombinant system, this CYP1B1 cDNA showed the lowest 17 beta-estradiol 4-hydroxylase activity among four different variant forms of CYP1B1, Thus, inter-individual differences in activation of procarcinogens or metabolism of oestrogen originating from genetic polymorphisms of the human CYP1B1 gene may contribute to the susceptibility of human cancers. Pharmacogenetics 10:25-33 (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:25 / 33
页数:9
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