Association of Vascular Endothelial Growth Factor Gene Polymorphisms with Susceptibility and Clinicopathologic Characteristics of Colorectal Cancer.
10.3346/jkms.2008.23.3.421
- Author:
Yee Soo CHAE
1
;
Jong Gwang KIM
;
Sang Kyun SOHN
;
Yoon Young CHO
;
Byung Min AHN
;
Joon Ho MOON
;
Seoung Woo JEON
;
Jae Yong PARK
;
In Taek LEE
;
Gyu Seog CHOI
;
Soo Han JUN
Author Information
1. Department of Oncology/Hematology, Kyungpook National University Hospital, Kyungpook National University School of Medicine, Daegu, Korea. jkk21c@knu.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Angiogenesis;
Colorectal Neoplasms;
Vascular Endothelial Growth Factors;
Polymorphism, Genetic
- MeSH:
Adult;
Aged;
Aged, 80 and over;
Colorectal Neoplasms/*epidemiology/*genetics/secondary;
Female;
Genetic Predisposition to Disease/epidemiology;
Haplotypes;
Humans;
Male;
Middle Aged;
Neovascularization, Pathologic/epidemiology/genetics/pathology;
*Polymorphism, Genetic;
Risk Factors;
Vascular Endothelial Growth Factor A/*genetics
- From:Journal of Korean Medical Science
2008;23(3):421-427
- CountryRepublic of Korea
- Language:English
-
Abstract:
Since vascular endothelial growth factor (VEGF) is known to be a potent pro-angiogenic factor, we evaluated the potential association of two VEGF gene polymorphisms (-634G>C and 936C>T) with the susceptibility and the clinicopathologic characteristics of colorectal cancer (CRC). The VEGF genotypes were determined using fresh colorectal tissue from 465 patients who had undergone a surgical resection and peripheral blood lymphocytes from 413 healthy controls by PCR/DHPLC assay. For the -634G>C polymorphism, the -634 GC or CC genotype was associated with a decreased risk of CRC (odds ratio [OR], 0.62; p=0.001) as a dominant model of C allele, whereas the 936 TT genotype correlated with advanced stage/ metastasis, a high serum level of CA19-9, and an higher grade in patients with CRC. In the haplotype analyses, haplotype -634C/936C and -634G/936T were associated with a decreased susceptibility of CRC (OR, 0.53 and 0.56; p<0.001, respectively). These observations imply that the VEGF gene polymorphisms may be associated with the susceptibility or clinicopathologic features of CRC. However, further studies of other VEGF sequence variants and their biological functions are needed to understand the role of the VEGF gene polymorphisms in the development and progression of CRC.
