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血管内皮生长因子多态性对肾细胞癌风险的预测价值:一项病例对照研究。

Predictive value of vascular endothelial growth factor polymorphisms on the risk of renal cell carcinomas: a case-control study.

作者信息

Lu Guangjian, Dong Yuqian, Zhang Qunmei, Jiao Luyang, Yang Shujuan, Shen Beili

机构信息

Clinical Laboratory, The First Affiliated Hospital of Xinxiang Medical University, Weihui, China.

Blood Transfusion Room, The First Affiliated Hospital of Xinxiang Medical University, Weihui, China.

出版信息

Tumour Biol. 2015 Nov;36(11):8645-52. doi: 10.1007/s13277-015-3431-1. Epub 2015 Jun 5.

Abstract

We conducted this case-control study to assess the role of vascular endothelial growth factor (VEGF) -2578C/A, +460T/C, +1612G/A, +936C/T, and -634G/C polymorphisms in the development of renal cell carcinoma (RCC), and analyzed the association of gene polymorphisms with demographic and clinical characteristics of RCC. This study included 412 consecutive primary RCC patients and 824 controls. The polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was performed to detect VEGF -2578C/A, +460T/C, +1612G/A, +936C/T, and -634G/C polymorphisms. Compared with the control subjects, the RCC cancer cases were more likely to have a habit of cigarette smoking, and suffered from hypertension and diabetes. Conditional logistic regression analysis showed that individuals carrying the AA genotype of -2578C/A were more likely to greatly increase risk of RCC, and the CC genotype of +460T/C revealed a significant association with increased risk of RCC. The CA + AA genotype of -2578C/A had a significantly increased risk of RCC in ever cigarette smokers, and individuals who suffered from hypertension and diabetes. TC + CC genotype of +460T/C was significantly associated with the elevated risk of RCC in those suffered from hypertension and diabetes. Our study suggests that -2578C/A and +460T/C polymorphisms of VEGF modulate the risk of developing RCC in Chinese population.

摘要

我们开展了这项病例对照研究,以评估血管内皮生长因子(VEGF)-2578C/A、+460T/C、+1612G/A、+936C/T和-634G/C基因多态性在肾细胞癌(RCC)发生中的作用,并分析基因多态性与RCC患者人口统计学和临床特征之间的关联。本研究纳入了412例连续的原发性RCC患者和824例对照。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法检测VEGF -2578C/A、+460T/C、+1612G/A、+936C/T和-634G/C基因多态性。与对照受试者相比,RCC患者更易有吸烟习惯,且患有高血压和糖尿病。条件逻辑回归分析显示,携带-2578C/A基因AA基因型的个体更易大幅增加患RCC的风险,+460T/C基因的CC基因型与RCC风险增加显著相关。-2578C/A基因的CA + AA基因型在曾经吸烟者以及患有高血压和糖尿病的个体中患RCC的风险显著增加。+460T/C基因的TC + CC基因型与患有高血压和糖尿病的个体中RCC风险升高显著相关。我们的研究表明,VEGF的-2578C/A和+460T/C基因多态性可调节中国人群患RCC的风险。

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