钙敏感受体986位丙氨酸-丝氨酸变异与结直肠癌风险

R. Dabiri, T. Mahmoudi, H. Farahani, H. Nobakht, M. Zali
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引用次数: 2

摘要

背景针对钙对结直肠癌(CRC)的作用,考虑到钙敏感受体(CaSR)在钙稳态中的关键作用,本研究探讨了CaSR基因rs1801725或A986S变异是否与结直肠癌的易感性相关。方法本研究采用病例-对照研究,纳入结直肠癌患者303例,对照组354例。采用PCR-RFLP方法对657例受试者进行CaSR基因A986S变异分型。结果CaSR基因A986S变异的基因型和等位基因频率在病例和对照组之间没有显著差异,即使在调整了年龄、BMI、性别、吸烟状况和CRC家族史后,这种差异仍然不显著。没有证据表明A986S变异与CRC的关联会因BMI、性别或肿瘤部位而改变。此外,我们还分别分析了正常体重(BMI < 25kg/m2)和超重/肥胖(BMI≥25kg/m2)受试者中A986S变异与肥胖风险的关系,结果发现正常体重(BMI < 25kg/m2)与超重/肥胖(BMI≥25kg/m2)受试者之间无显著差异。结论:我们的研究结果不支持CaSR基因A986S变异在结直肠癌风险中的作用;然而,这一发现还有待证实,该基因变异在癌变中的作用还有待进一步研究。
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Alanine to Serine Variant at Position 986 of Calcium Sensing Receptor and Colorectal Cancer Risk
Background With regard to the effect of calcium against colorectal cancer (CRC) and considering the key role of calcium sensing receptor (CaSR) in calcium homeostasis, this study investigated whether CaSR gene rs1801725 or A986S variant was associated with susceptibility to CRC risk. Methods This study was conducted as a case-control study and 303 cases with CRC and 354 controls were enrolled. All 657 subjects were genotyped for CaSR gene A986S variant using PCR-RFLP method. Results No significant difference was observed for the A986S variant of CaSR gene in either genotype or allele frequencies between the cases and the controls and this lack of difference remained non-significant even after adjustment for age, BMI, sex, smoking status, and family history of CRC. No evidence for the effect modification of the association A986S variant and CRC by BMI, sex, or tumor site was also observed. Furthermore, the risk of obesity in relation to the A986S variant in the controls and the cases was separately analyzed and we observed no significant difference between normal weight (BMI < 25kg/m2) and overweight/obese (BMI ≥ 25kg/m2) subjects. Conclusions Our findings do not support a role for effect of the CaSR gene A986S variant on CRC risk; nevertheless, this finding requires confirmation and the role of the gene variant in carcinogenesis needs to be further investigated.
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