Polymorphisms in the CYP19A1 (Aromatase) gene and endometrial cancer risk in Chinese women

被引:31
作者
Tao, Meng Hua
Cai, Qiuyin
Zhang, Zuo-Feng
Xu, Wang-Hong
Kataoka, Nobuhiko
Wen, Wanqing
Xiang, Yong-Bing
Zheng, Wei
Shu, Xiao Ou
机构
[1] Vanderbilt Univ, Sch Med, Med Ctr, Vanderbilt Epidemiol Ctr,Dept Med, Nashville, TN 37203 USA
[2] Vanderbilt Univ, Ingram Canc Ctr, Nashville, TN USA
[3] Univ Calif Los Angeles, Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA 90024 USA
[4] SUNY Buffalo, Sch Publ Hlth & Hlth Profess, Dept Social & Prevent Med, Buffalo, NY 14260 USA
[5] Shanghai Canc Inst, Dept Epidemiol, Shanghai, Peoples R China
关键词
D O I
10.1158/1055-9965.EPI-06-1012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aromatase, encoded by the CYP19A1 gene, is a key enzyme in estradiol biosynthesis, which catalyzes the conversion of androstenedione and testosterone to estrone and estradiol, respectively. Given the critical role of estrogen in the development of endometrial cancer risk, we evaluated genetic polymorphisms of the CYP19A1 gene, including rs1065779, rs700519, rs28566535, rs752760, and rs1870050, in association with endometrial cancer in a population-based case-control study conducted in Shanghai, China. Genotypes of 1,040 incident endometrial cancer cases and 1,031 frequency-matched controls were included in the study. We applied a logistic regression model to derive adjusted odds ratios (OR) and their 95% confidence intervals (95% CI). Six common haplotypes with a frequency >= 5% were estimated; the highest frequency haplotype was GCACA (27.8% in cases and 26.2% in controls). We observed an inverse association between CYP19A1 haplotype TCATC and endometrial cancer in our population (OR, 0.76; 95% CI, 0.62-0.92). An inverse association was found between endometrial cancer and single nucleotide polymorphism rs1870050 in the promoter region with ORs of 0.81 (95% CI, 0.68-0.97) and 0.58 (95% CI, 0.42-0.80) for the AC and CC genotypes, respectively. We observed a multiplicative interaction between single nucleotide polymorphism rs700519 and body mass index among postmenopausal women (P = 0.01), with stronger associations between rs700519 genotypes and endometrial cancer risk among heavier (body mass index, >= 25) postmenopausal women. In summary, our data show that polymorphisms in the CYP19A1 gene may contribute to endometrial carcinogenesis.
引用
收藏
页码:943 / 949
页数:7
相关论文
共 40 条
[1]   Role of exogenous and endogenous hormones in endometrial cancer - Review of the evidence and research perspectives [J].
Akhmedkhanov, A ;
Zeleniuch-Jacquotte, A ;
Toniolo, P .
HUMAN FERTILITY AND REPRODUCTION: THE OOCYTE, THE EMBRYO, AND THE UTERUS, 2001, 943 :296-315
[2]  
ASHAN H, 2005, BREAST CANCER RES, V7, pR71
[3]  
Berstein L, 2005, NEOPLASMA, V52, P115
[4]   CYP19 gene polymorphism in endometrial cancer patients [J].
Berstein, LM ;
Imyanitov, EN ;
Suspitsin, EN ;
Grigoriev, MY ;
Sokolov, EP ;
Togo, A ;
Hanson, KP ;
Poroshina, TE ;
Vasiljev, DA ;
Kovalevskij, AY ;
Gamajunova, VB .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2001, 127 (02) :135-138
[5]   CYP19 (AROMATASE CYTOCHROME-P450) GENE-EXPRESSION IN HUMAN-MALIGNANT ENDOMETRIAL TUMORS [J].
BULUN, SE ;
ECONOMOS, K ;
MILLER, D ;
SIMPSON, ER .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (06) :1831-1834
[6]  
Bulun SE, 1997, J STEROID BIOCHEM, V61, P133
[7]   The human CYP19 (aromatase P450) gene:: update on physiologic roles and genomic organization of promoters [J].
Bulun, SE ;
Sebastian, S ;
Takayama, K ;
Suzuki, T ;
Sasano, H ;
Shozu, M .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2003, 86 (3-5) :219-224
[8]   Functional Ser326Cys polymorphism in the hOGG1 gene is not associated with breast cancer risk [J].
Cai, QY ;
Shu, XO ;
Wen, WQ ;
Courtney, R ;
Dai, Q ;
Gao, YT ;
Zheng, W .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2006, 15 (02) :403-404
[9]   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
[10]  
Fukatsu T, 2004, ANTICANCER RES, V24, P2431