Genetic polymorphisms of phase I metabolizing enzyme genes, their interaction with lifetime grilled and smoked meat intake, and breast cancer incidence

被引:13
作者
Parada, Humberto, Jr. [1 ]
Steck, Susan E. [2 ]
Cleveland, Rebecca J. [3 ]
Teitelbaum, Susan L. [4 ]
Neugut, Alfred I. [5 ,6 ]
Santella, Regina M. [7 ]
Gammon, Marilie D. [1 ]
机构
[1] Univ N Carolina, Dept Epidemiol, Gillings Sch Global Publ Hlth, Chapel Hill, NC USA
[2] Univ South Carolina, Arnold Sch Publ Hlth, Dept Epidemiol & Biostat, Columbia, SC 29208 USA
[3] Univ N Carolina, Sch Med, Dept Med, Chapel Hill, NC USA
[4] Icahn Sch Med Mt Sinai, Dept Prevent Med, New York, NY 10029 USA
[5] Columbia Univ, Coll Phys & Surg, Dept Med, New York, NY USA
[6] Columbia Univ, Mailman Sch Publ Hlth, Dept Epidemiol, New York, NY USA
[7] Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY USA
关键词
Breast cancer; Cytochrome p450 enzymes; Polymorphism; Grilled and smoked meat; Gene-environment interactions; POLYCYCLIC AROMATIC-HYDROCARBONS; RISK-FACTORS; LONG-ISLAND; SUSCEPTIBILITY; ASSOCIATION; CYP1B1; CONSUMPTION; EXPRESSION; PAH;
D O I
10.1016/j.annepidem.2016.11.005
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose:To examine associations between 22 CYP single nucleotide polymorphisms (SNPs) and breast cancer incidence and their interactions with grilled smoked meat intake, a source of polycyclic aromatic hydrocarbons. Methods: White women with first primary in situ or invasive breast cancer (n = 988) and frequency matched controls (n = 1021) from a population-based study were interviewed to assess lifetime grilled smoked meat intake. SNPs with minor allele frequencies of greater than 0.05 were selected because of their links to carcinogenesis. We used multivariable unconditional logistic regression to estimate odds ratios (ORs) and 95% confidence intervals (CIs). Results: Breast cancer was inversely associated with CYP1A1 rs104C8943 AG + GG genotype (OR = 0.71, 95% CI = 0.50-0.99; vs. AA genotype) and positively associated with CYP1B1 rs10175338 TT genotype (OR = 1.59, 95% CI = 1.12-2.26; vs. GG genotype) and the CYP3A4 rs2242480 CT + IT genotype (OR = 1.25, 95% CI = 1.00-1.56; vs. CC genotype). The sum of the number of "at-risk" alleles for the CYP SNPs was positively associated with breast cancer incidence (4-6 "at-risk" alleles OR = 2.33, 95% CI = 1.37-3.99 vs. 0-1 alleles; -,14rend <.01). We observed multiplicative and additive interactions (P <.05) between grilled smoked meat intake (low vs. high) with CYP1A1 rs1048943 and CYPIBI rs10175338 SNPs. Conclusions: Phase I metabolizing enzyme gene SNPs may play a role in breast cancer development and may modify the grilled smoked meat intake breast cancer association.
引用
收藏
页码:208 / 214
页数:7
相关论文
共 45 条
[1]  
AMBROSONE CB, 1995, CANCER RES, V55, P3483
[2]  
[Anonymous], PUBL HLTH STAT POL A
[3]  
[Anonymous], VET WORLD
[4]   THE RELATIVE VALIDITY OF A RETROSPECTIVE ESTIMATE OF FOOD-CONSUMPTION BASED ON A CURRENT DIETARY HISTORY AND A FOOD FREQUENCY LIST [J].
BAKKUM, A ;
BLOEMBERG, B ;
VANSTAVEREN, WA ;
VERSCHUREN, M ;
WEST, CE .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1988, 11 (01) :41-53
[5]   Breast cancer susceptibility genes analysed into three groups Genomics and breast cancer: the different levels of inherited susceptibility [J].
Beggs, Andrew D. ;
Hodgson, Shirley V. .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2009, 17 (07) :855-856
[6]  
Byers T E, 1983, Nutr Cancer, V5, P69, DOI 10.1080/01635588309513781
[7]   COMPARATIVE DOSE-RESPONSE TUMORIGENICITY STUDIES OF DIBENZO[A,L]PYRENE VERSUS 7,12-DIMETHYLBENZ[A]ANTHRACENE, BENZO[A]PYRENE AND 2 DIBENZO[A,L]PYRENE DIHYDRODIOLS IN MOUSE SKIN AND RAT MAMMARY-GLAND [J].
CAVALIERI, EL ;
HIGGINBOTHAM, S ;
RAMAKRISHNA, NVS ;
DEVANESAN, PD ;
TODOROVIC, R ;
ROGAN, EG ;
SALMASI, S .
CARCINOGENESIS, 1991, 12 (10) :1939-1944
[8]  
Dai Q, 2002, CANCER EPIDEM BIOMAR, V11, P801
[9]  
DeStefani E, 1997, CANCER EPIDEM BIOMAR, V6, P573
[10]   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