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维生素 D 受体基因起始密码子 FokI 和内含子 8 BsmI 多态性与结直肠癌易感性的关系。

Start codon FokI and intron 8 BsmI variants in the vitamin D receptor gene and susceptibility to colorectal cancer.

机构信息

Department of Cancer, Research Center for Gastroenterology and Liver Diseases (RCGLD), Shahid Beheshti University of Medical Sciences, Velenjak, Shahid Chamran Highway, 1985711151 Tehran, Iran.

出版信息

Mol Biol Rep. 2011 Oct;38(7):4765-70. doi: 10.1007/s11033-010-0613-1. Epub 2010 Dec 4.

Abstract

Epidemiological evidence suggests the protective effect of vitamin D against colorectal cancer (CRC) and the polymorphisms in vitamin D receptor (VDR) gene may influence the development of CRC. In this study the possible association of VDR FokI and BsmI gene polymorphisms with CRC risk was examined. A total of 904 subjects, including 452 cases with CRC and 452 controls were enrolled in this study. All 904 subjects were genotyped for VDR FokI and BsmI gene polymorphisms by PCR-RFLP method. We observed no significant difference in genotype and allele frequencies between the cases with CRC and controls for the both FokI and BsmI polymorphisms either before or after adjustment for confounding factors including age, BMI, sex, and smoking status. Furthermore, no evidence for effect modification of the association VDR gene FokI and BsmI variants and CRC by BMI, sex, or tumor site was observed. In addition, there was no significant difference in genotype and allele frequencies between the normal weight (BMI <25 kg/m(2)) cases with CRC and overweight/obese (BMI ≥25 kg/m(2)) cases with CRC for the two SNPs. Our results do not lend support to the hypothesis that VDR gene FokI and BsmI polymorphisms are associated with the risk of CRC. However, further studies are required to confirm this finding.

摘要

流行病学证据表明,维生素 D 对结直肠癌(CRC)具有保护作用,维生素 D 受体(VDR)基因的多态性可能影响 CRC 的发展。本研究旨在探讨 VDR FokI 和 BsmI 基因多态性与 CRC 风险的相关性。本研究共纳入 904 例受试者,包括 452 例 CRC 患者和 452 例对照。采用 PCR-RFLP 法检测所有 904 例受试者的 VDR FokI 和 BsmI 基因多态性。我们发现,无论是否调整年龄、BMI、性别和吸烟状况等混杂因素,CRC 患者与对照组在 FokI 和 BsmI 多态性的基因型和等位基因频率方面均无显著差异。此外,未观察到 VDR 基因 FokI 和 BsmI 变异与 CRC 之间存在 BMI、性别或肿瘤部位的交互作用。此外,对于这两个 SNP,BMI<25kg/m2 的 CRC 患者与 BMI≥25kg/m2 的 CRC 患者在基因型和等位基因频率方面无显著差异。我们的研究结果不支持 VDR 基因 FokI 和 BsmI 多态性与 CRC 风险相关的假说。然而,还需要进一步的研究来证实这一发现。

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