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北印度人群中血管内皮生长因子(VEGF)及血管内皮生长因子受体1(VEGFR1)基因多态性与乳腺癌风险的关联

Association of VEGF and VEGFR1 polymorphisms with breast cancer risk in North Indians.

作者信息

Kapahi Ruhi, Guleria Kamlesh, Sambyal Vasudha, Manjari Mridu, Sudan Meena, Uppal Manjit Singh, Singh Neeti Rajan

机构信息

Human Cytogenetics Laboratory, Department of Human Genetics, Guru Nanak Dev University, Amritsar, 143005, Punjab, India.

出版信息

Tumour Biol. 2015 Jun;36(6):4223-34. doi: 10.1007/s13277-015-3059-1. Epub 2015 Jan 22.

Abstract

The aim of present study was to evaluate the relationship between vascular endothelial growth factor (VEGF) -2578C/A, -2549I/D, -460T/C and -7C/T and VEGFR1 -710C/T polymorphisms with risk to breast cancer in North Indians. A total of 204 sporadic breast cancer patients and 204 controls were recruited for this case-control study. Significantly increased frequency of II genotype of -2549I/D polymorphism was observed in patients as compared to control individuals (odds ratio (OR) = 2.76, 95 % confidence interval (CI), 1.55-4.92; p = 0.0005). VEGF -2578AA genotype (OR = 2.87; 95 % CI, 1.61-5.10; p = 0.0003) and A allele (OR = 1.65, 95 % CI, 1.25-2.18; p = 0.0004) were found to be associated with increased risk for breast cancer. Individuals carrying CC genotype (OR = 2.23, 95 % CI, 1.25-3.97) and C allele (OR = 1.42, 95 % CI, 1.07-1.87) of VEGF -460T/C polymorphism were at higher risk of breast cancer. There was no significant difference in genotype and allele distribution of VEGF -7C/T and VEGFR1 -710C/T polymorphisms between cases and control individuals (p > 0.05). Linkage disequilibrium analysis showed a strong linkage between VEGF -2549I/D and -2578C/A polymorphisms (Lewontin's [Formula: see text] = 0.99; r (2) = 0.97), -2549I/D and -460T/C ([Formula: see text] = 0.94; r (2) = 0.84), and -2578C/A and -460T/C polymorphisms ([Formula: see text] = 0.93; r (2) = 0.83). In the present study, we concluded that VEGF -2549I/D, -2578C/A and -460T/C polymorphisms are associated with risk to breast cancer in Punjab, North India.

摘要

本研究旨在评估血管内皮生长因子(VEGF)-2578C/A、-2549I/D、-460T/C和-7C/T以及血管内皮生长因子受体1(VEGFR1)-710C/T基因多态性与北印度人患乳腺癌风险之间的关系。本病例对照研究共招募了204例散发性乳腺癌患者和204名对照个体。与对照个体相比,患者中-2549I/D基因多态性的II基因型频率显著增加(优势比(OR)=2.76,95%置信区间(CI),1.55 - 4.92;p = 0.0005)。发现VEGF -2578AA基因型(OR = 2.87;95% CI,1.61 - 5.10;p = 0.0003)和A等位基因(OR = 1.65,95% CI,1.25 - 2.18;p = 0.0004)与乳腺癌风险增加相关。携带VEGF -460T/C基因多态性CC基因型(OR = 2.23,95% CI,1.25 - 3.97)和C等位基因(OR = 1.42,95% CI,1.07 - 1.87)的个体患乳腺癌的风险更高。病例组和对照组个体之间VEGF -7C/T和VEGFR1 -710C/T基因多态性的基因型和等位基因分布没有显著差异(p > 0.05)。连锁不平衡分析显示VEGF -2549I/D与-2578C/A基因多态性之间存在强连锁(Lewontin's [公式:见正文] = 0.99;r(2) = 0.97),-2549I/D与-460T/C([公式:见正文] = 0.94;r(2) = 0.84),以及-2578C/A与-460T/C基因多态性之间存在强连锁([公式:见正文] = 0.93;r(2) = 0.83)。在本研究中,我们得出结论,VEGF -2549I/D、-2578C/A和-460T/C基因多态性与印度北部旁遮普邦的乳腺癌风险相关。

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