Three polymorphisms in cytochrome P450 1B1 (CYP1B1) gene and breast cancer risk: a meta-analysis

被引:38
作者
Economopoulos, Konstantinos P. [1 ,2 ]
Sergentanis, Theodoros N. [1 ,2 ]
机构
[1] Soc Jr Doctors, Athens, Greece
[2] Natl Tech Univ Athens, Sch Med, Athens, Greece
关键词
CYP1B1; Cytochrome P450; Polymorphism; Breast cancer; Arg48Gly; Ala119Ser; Asn453Ser; POLYCYCLIC AROMATIC-HYDROCARBONS; SEX-HORMONE METABOLISM; ESTROGEN-METABOLISM; P450; 1A1; ASSOCIATION; SUSCEPTIBILITY; ACTIVATION; VARIANTS; PATHWAY;
D O I
10.1007/s10549-009-0728-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cytochrome P450 1B1 (CYP1B1) is a P450 enzyme implicated in the metabolism of exogenous and endogenous substrates. The metabolism of polycyclic aromatic hydrocarbons and other procarcinogens through CYP1B1 may well lead to their activation. Apart from the extensively studied Val432Leu polymorphism, three single nucleotide polymorphisms in CYP1B1 have been studied concerning their potential implication in terms of breast cancer risk: Arg48Gly, Ala119Ser and Asn453Ser. This meta-analysis aims to examine whether the three aforementioned polymorphisms are associated with breast cancer risk. Eligible articles were identified by a search of MEDLINE bibliographical database for the period up to December 2009. Concerning Arg48Gly polymorphism, 10 studies were eligible (11,321 cases and 13,379 controls); 11 studies were eligible for Ala119Ser (10,715 cases and 11,678 controls); 12 cases were eligible regarding Asn453Ser (11,630 cases and 14,053 controls). Pooled odds ratios (OR) were appropriately derived form fixed-effects or random-effects models. Sensitivity analysis excluding studies whose genotype frequencies in controls significantly deviated from Hardy-Weinberg equilibrium was performed. Concerning Arg48Gly, the pooled ORs (95% CI) were 0.933 (0.808-1.078) for heterozygous and 0.819 (0.610-1.100) for homozygous Gly subjects. Regarding Ala119Ser, the pooled ORs were 0.992 (0.896-1.097) for heterozygous and 0.935 (0.729-1.198) for homozygous Ser subjects. With respect to Asn453Ser, the pooled ORs were 0.961 (0.906-1.019) for heterozygous and 0.984 (0.846-1.144) for homozygous Ser subjects. In conclusion, this meta-analysis suggests that CYP1B1 Arg48Gly, Ala119Ser and Asn453Ser polymorphisms are not associated with breast cancer risk. Studies on Chinese populations are needed, to elucidate race-specific effects on East Asian populations, if any.
引用
收藏
页码:545 / 551
页数:7
相关论文
共 43 条
[1]   A family-based genetic association study of variants in estrogen-metabolism genes COMT and CYP1B1 and breast cancer risk [J].
Ahsan, H ;
Chen, Y ;
Whittemore, AS ;
Kibriya, MG ;
Gurvich, I ;
Senie, RT ;
Santella, RM .
BREAST CANCER RESEARCH AND TREATMENT, 2004, 85 (02) :121-131
[2]  
Bailey LR, 1998, CANCER RES, V58, P5038
[3]   Genetic polymorphisms in phase I and phase II enzymes and breast cancer risk associated with menopausal hormone therapy in postmenopausal women [J].
Chang-Claude, Jenny ;
Beckmann, Lars ;
Corson, Charlotte ;
Hein, Rebecca ;
Kropp, Silke ;
Parthimos, Margie ;
Duennebier, Thomas ;
Hamann, Ute ;
Brors, Benedikt ;
Eils, Roland ;
Zapatka, Marc ;
Brauch, Hiltrud ;
Justenhoven, Christina ;
Flesch-Janys, Dieter ;
Braendle, Wilhelm ;
Bruening, Thomas ;
Pesch, Beate ;
Spickenheuer, Anne ;
Ko, Yon-Dschun ;
Baisch, Christian ;
Dahmen, Norbert .
BREAST CANCER RESEARCH AND TREATMENT, 2010, 119 (02) :463-474
[4]  
De Vivo I, 2002, CANCER EPIDEM BIOMAR, V11, P489
[5]   Polymorphisms in genes involved in sex hormone metabolism, estrogen plus progestin hormone therapy use, and risk of postmenopausal breast cancer [J].
Diergaarde, Brenda ;
Potter, John D. ;
Jupe, Eldon R. ;
Manjeshwar, Sharmila ;
Shimasaki, Craig D. ;
Pugh, Thomas W. ;
DeFreese, Daniele C. ;
Gramling, Bobby A. ;
Evans, Ilonka ;
White, Emily .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2008, 17 (07) :1751-1759
[6]   Polymorphisms associated with circulating sex hormone levels in postmenopausal women [J].
Dunning, AM ;
Dowsett, M ;
Healey, CS ;
Tee, L ;
Luben, RN ;
Folkerd, E ;
Novik, KL ;
Kelemen, L ;
Ogata, S ;
Pharoah, PDP ;
Easton, DF ;
Day, NE ;
Ponder, BAJ .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (12) :936-945
[7]   XRCC3 Thr241Met polymorphism and breast cancer risk: a meta-analysis [J].
Economopoulos, Konstantinos P. ;
Sergentanis, Theodoros N. .
BREAST CANCER RESEARCH AND TREATMENT, 2010, 121 (02) :439-443
[8]   Differential effects of MDM2 SNP309 polymorphism on breast cancer risk along with race: a meta-analysis [J].
Economopoulos, Konstantinos P. ;
Sergentanis, Theodoros N. .
BREAST CANCER RESEARCH AND TREATMENT, 2010, 120 (01) :211-216
[9]   Bias in meta-analysis detected by a simple, graphical test [J].
Egger, M ;
Smith, GD ;
Schneider, M ;
Minder, C .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 315 (7109) :629-634
[10]   Intra-individual variation and sex differences in gene expression of cytochromes P450 in circulating leukocytes [J].
Finnström N. ;
Ask B. ;
Dahl M.-L. ;
Gadd M. ;
Rane A. .
The Pharmacogenomics Journal, 2002, 2 (2) :111-116