The VEGF-634G>C promoter polymorphism is associated with risk of gastric cancer

被引:42
作者
Guan, Xiaoxiang [1 ]
Zhao, Hui [1 ]
Niu, Jiangong [1 ]
Tang, Dongfeng [2 ]
Ajani, Jaffer A. [3 ]
Wei, Qingyi [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
ENDOTHELIAL GROWTH-FACTOR; CYTOKINE GENE POLYMORPHISMS; BREAST-CANCER; TRANSFORMING-GROWTH-FACTOR-BETA-1; GENE; TGF-BETA-1; VEGF GENE; TGF-BETA; EPIDEMIOLOGY; CARCINOMA;
D O I
10.1186/1471-230X-9-77
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Both TGF-beta 1 and VEGF play a critic role in the multiple-step process of tumorgenesis of gastric cancer. Single nucleotide polymorphisms (SNPs) of the TGFB1 and VEGF genes have been associated with risk and progression of many cancers. In this study, we investigated the association between potentially functional SNPs of these two genes and risk of gastric cancer in a US population. Methods: The risk associated with genotypes and haplotypes of four TGFB1 SNPs and four VEGF SNPs were determined by multivariate logistic regression analysis in 171 patients with gastric cancer and 353 cancer-free controls frequency-matched by age, sex and ethnicity. Results: Compared with the VEGF-634GG genotype, the -634CG genotype and the combined 634CG+CC genotypes were associated with a significantly elevated risk of gastric cancer (adjusted OR = 1.88, 95% CI = 1.24-2.86 and adjusted OR = 1.56, 95% CI = 1.07-2.27, respectively). However, none of other TGFB1 and VEGF SNPs was associated with risk of gastric cancer. Conclusion: Our data suggested that the VEGF-634G>C SNP may be a marker for susceptibility to gastric cancer, and this finding needs to be validated in larger studies.
引用
收藏
页数:7
相关论文
共 38 条
[1]   Potentially functional single nucleoticle polymorphisms in the core nucleoticle excision repair genes and risk of squamous cell carcinoma of the head and neck [J].
An, Jiaze ;
Liu, Zhensheng ;
Hu, Zhibin ;
Li, Guojun ;
Wang, Li-E ;
Sturgis, Erich M. ;
El-Naggar, Adel K. ;
Spitz, Margaret R. ;
Wei, Qingyi .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2007, 16 (08) :1633-1638
[2]   Investigation of vascular endothelial growth factor gene Polymorphisms and its association with clinicopathologic characteristics in gastric cancer [J].
Chae, Yee Soo ;
Kim, Jong Gwang ;
Sohn, Sang Kyun ;
Cho, Yoon Young ;
Moon, Joon Ho ;
Bae, Han-Ik ;
Park, Jae Yong ;
Lee, Myung-Hoon ;
Lee, Hyun-Chul ;
Chung, Ho Young ;
Yu, Wansik .
ONCOLOGY, 2006, 71 (3-4) :266-272
[3]  
CORREA P, 1975, LANCET, V2, P58
[4]   Infusion reactions to infliximab in children and adolescents: frequency, outcome and a predictive model [J].
Crandall, WV ;
Mackner, LM .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (01) :75-84
[5]   Epidemiology of gastric cancer [J].
Crew, Katherine D. ;
Neugut, Alfred I. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2006, 12 (03) :354-362
[6]  
Dunning AM, 2003, CANCER RES, V63, P2610
[7]  
Ewart-Toland A, 2004, CANCER EPIDEM BIOMAR, V13, P759
[8]   Meta-analysis: tumour invasion-related genetic polymorphisms and gastric cancer susceptibility [J].
Gao, L. ;
Nieters, A. ;
Brenner, H. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2008, 28 (05) :565-573
[9]   Influence of vascular endothelial growth factor single nucleotide polymorphisms on tumour development in cutaneous malignant melanoma [J].
Howell, WM ;
Bateman, A ;
Turner, SJ ;
Collins, A ;
Theaker, JM .
GENES AND IMMUNITY, 2002, 3 (04) :229-232
[10]   Polymorphisms in the vascular endothelial growth factor gene and breast cancer in the Cancer Prevention Study II cohort [J].
Jacobs, EJ ;
Feigelson, HS ;
Bain, EB ;
Brady, KA ;
Rodriguez, C ;
Stevens, VL ;
Patel, AV ;
Thun, MJ ;
Calle, EE .
BREAST CANCER RESEARCH, 2006, 8 (02)