Kapahi Ruhi, Manjari Mridu, Sudan Meena, Uppal Manjit Singh, Singh Neeti Rajan, Sambyal Vasudha, Guleria Kamlesh
Human Cytogenetics Laboratory, Department of Human Genetics, Guru Nanak Dev University, Punjab, India E-mail :
Asian Pac J Cancer Prev. 2014;15(1):257-63. doi: 10.7314/apjcp.2014.15.1.257.
Vascular endothelial growth factor (VEGF), an endothelial cell specific mitogen, has been implicated as a critical factor influencing tumor related angiogenesis. The aim of present study was to evaluate the relationship between VEGF +936C>T and +405C>G polymorphisms of VEGF with risk of breast cancer in Punjab, India.
We screened DNA samples of 192 sporadic breast cancer patients and 192 unrelated healthy, gender and age matched control individuals for VEGF +936C>T and +405C>G polymorphisms using the PCR-RFLP method.
For the VEGF +405C>G polymorphism, we observed significantly increased frequency of GG genotype in cases as compared to controls and strong association of +405GG genotype was observed with three fold risk for breast cancer (OR=3.07; 95%CI 1.41-6.65; p=0.003). For the +936C>T polymorphism, significant associations of CT and combined CT+TT genotypes were observed with elevated risk of breast cancer (p=0.021; 0.023). The combined genotype combinations of GG-CC and GG- CT of +405C>G and +936C>T polymorphisms were found to be significantly associated with increased risk of breast cancer (p=0.04; 0.0064).
The findings of the present study indicated significant associations of VEGF +936C>T and +405C>G polymorphisms with increased breast cancer risk in patients from Punjab, North India.
血管内皮生长因子(VEGF)是一种内皮细胞特异性有丝分裂原,被认为是影响肿瘤相关血管生成的关键因素。本研究旨在评估印度旁遮普邦VEGF基因+936C>T和+405C>G多态性与乳腺癌风险之间的关系。
我们采用PCR-RFLP方法,对192例散发性乳腺癌患者以及192名年龄和性别匹配的健康对照个体的DNA样本进行VEGF +936C>T和+405C>G多态性筛查。
对于VEGF +405C>G多态性,我们观察到病例组中GG基因型的频率显著高于对照组,并且发现+405GG基因型与乳腺癌风险增加三倍相关(OR=3.07;95%CI 1.41-6.65;p=0.003)。对于+936C>T多态性,观察到CT基因型以及CT+TT合并基因型与乳腺癌风险升高显著相关(p=0.021;0.023)。发现+405C>G和+936C>T多态性的GG-CC和GG-CT合并基因型组合与乳腺癌风险增加显著相关(p=0.04;0.0064)。
本研究结果表明,在印度北部旁遮普邦的患者中,VEGF +936C>T和+405C>G多态性与乳腺癌风险增加显著相关。