Relationship between growth hormone 1 genetic polymorphism and susceptibility to colorectal cancer

被引:8
作者
Gao, Chang-Ming [1 ]
Gong, Jian-Ping [1 ]
Wu, Jian-Zhong [1 ]
Cao, Hai-Xia [1 ]
Ding, Jian-Hua [1 ]
Zhou, Jian-Nong [1 ]
Liu, Yan-Ting [1 ]
Li, Su-Ping [1 ]
Cao, Jia [2 ]
Matsuo, Keitaro [3 ]
Takezaki, Toshiro [4 ]
Tajima, Kazuo [3 ]
机构
[1] Jiangsu Prov Inst Canc Res, Div Epidemiol, Nanjing 210009, Jiangsu Prov, Peoples R China
[2] Third Mil Med Univ, Prevent Med Coll, Hygiene Toxicol Dept, Chongqing, Peoples R China
[3] Aichi Canc Ctr, Res Inst, Div Epidemiol & Prevent, Nagoya, Aichi 464, Japan
[4] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Int Isl & Community Med, Kagoshima 890, Japan
基金
中国国家自然科学基金;
关键词
alcohol drinking; colorectal cancer; genetic polymorphism; growth hormone 1; smoking; IGF-BINDING PROTEIN-3; LIFE-STYLE FACTORS; FACTOR-I; CIGARETTE-SMOKING; FACTOR (IGF)-I; PLASMA-LEVELS; ELDERLY-MEN; RISK; ASSOCIATION; NEOPLASIA;
D O I
10.1038/jhg.2010.3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The aim of this study was to evaluate the relationship between smoking, alcohol drinking and genetic polymorphism of the growth hormone 1 gene (GH1) T1663A with reference to colorectal cancer. We conducted a case-control study with 315 cases of colorectal cancer and 438 population-based controls in the Jiangsu Province, China. GH1 T1663A genotypes were identified using PCR-RFLP (restriction fragment length polymorphism) methods. Information on smoking and drinking was collected using a questionnaire. Odds ratios (ORs) were estimated with an unconditional logistic model. The distribution of T/T and A/A genotypes was significantly different between controls and cases (chi(2)(MH)=3.877, P=0.049). Compared with the GH1 T/T genotype, the A/A genotype was at a decreased risk of developing colorectal cancer (sex-, age-, body mass index-, smoking- and alcohol drinking-adjusted OR=0.56, 95% confidence interval: 0.34-0.90). Smoking was not associated with the risk of colorectal cancer, whereas alcohol drinking was associated with an increased risk of colorectal cancer. Among nonsmokers or nondrinkers, individuals who had the GH1 A/A genotype were at a decreased risk of developing colorectal cancer compared with individuals who had the GH1 T allele. These results show that the GH1 T1663A A/A genotype can decrease the risk for colorectal cancer. Journal of Human Genetics (2010) 55, 163-166; doi: 10.1038/jhg.2010.3; published online 19 February 2010
引用
收藏
页码:163 / 166
页数:4
相关论文
共 21 条
[1]   Polymorphisms of alcohol dehydrogenase 2 and aldehyde dehydrogenase 2 and colorectal cancer risk in Chinese males [J].
Gao, Chang-Ming ;
Takezaki, Toshiro ;
Wu, Jian-Zhong ;
Zhang, Xiao-Mei ;
Cao, Hai-Xia ;
Ding, Jian-Hua ;
Liu, Yan-Ting ;
Li, Su-Ping ;
Cao, Jia ;
Matsuo, Keitaro ;
Hamajima, Nobuyuki ;
Tajima, Kazuo .
WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (32) :5078-5083
[2]   CP2E1 Rsa I polymorphism impacts on risks of colorectal cancer association with smoking and alcohol drinking [J].
Gao, Chang-Ming ;
Takezaki, Toshiro ;
Wu, Jian-Zhong ;
Chen, Min-Bin ;
Liu, Yan-Ting ;
Ding, Ian-Hua ;
Sugimura, Haruhiko ;
Cao, Lia ;
Hamajima, Nobuyuki ;
Tajima, Kazuo .
WORLD JOURNAL OF GASTROENTEROLOGY, 2007, 13 (43) :5725-5730
[3]  
Gapstur SM, 2004, CANCER EPIDEM BIOMAR, V13, P2208
[4]  
Giovannucci E, 2000, CANCER EPIDEM BIOMAR, V9, P345
[5]   Epidemiology of insulin-like growth factor-I in elderly men and women - The Rancho Bernardo Study [J].
GoodmanGruen, D ;
BarrettConnor, E .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1997, 145 (11) :970-976
[6]   Identification of novel human GH-1 gene polymorphisms that are associated with growth hormone secretion and height [J].
Hasegawa, Y ;
Fujii, K ;
Yamada, M ;
Igarashi, Y ;
Tachibana, K ;
Tanaka, T ;
Onigata, K ;
Nishi, Y ;
Kato, S ;
Hasegawa, T .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (03) :1290-1295
[7]   Growth hormone, IGF-I and cancer. Less intervention to avoid cancer? More intervention to prevent cancer? [J].
Holly, JMP ;
Gunnell, DJ ;
Smith, GD .
JOURNAL OF ENDOCRINOLOGY, 1999, 162 (03) :321-330
[8]   Insulin-like growth factor I and the development of colorectal neoplasia in acromegaly [J].
Jenkins, PJ ;
Frajese, V ;
Jones, AM ;
Camacho-Hubner, C ;
Lowe, DG ;
Fairclough, PD ;
Chew, SL ;
Grossman, AB ;
Monson, JP ;
Besser, GM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (09) :3218-3221
[9]   Acromegaly, colonic polyps and carcinoma [J].
Jenkins, PJ ;
Fairclough, PD ;
Richards, T ;
Lowe, DG ;
Monson, J ;
Grossman, A ;
Wass, JAH ;
Besser, M .
CLINICAL ENDOCRINOLOGY, 1997, 47 (01) :17-22
[10]   Serum C-peptide, insulin-like growth factor (IGF)-I, IGF-binding proteins, and colorectal cancer risk in women [J].
Kaaks, R ;
Toniolo, P ;
Akhmedkhanov, A ;
Lukanova, A ;
Biessy, C ;
Dechaud, H ;
Rinaldi, S ;
Zeleniuch-Jacquotte, A ;
Shore, RE ;
Riboli, E .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (19) :1592-1600