Dabiri Reza, Mahmoudi Touraj, Farahani Hamid, Nobakht Hossein, Zali Mohammad Reza
Internal Medicine Department, Semnan University of Medical Sciences, Semnan, IR Iran.
Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, IR Iran.
Iran J Cancer Prev. 2016 Aug 9;9(4):e8098. doi: 10.17795/ijcp-8098. eCollection 2016 Aug.
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 gene rs1801725 or A986S variant was associated with susceptibility to CRC risk.
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 gene A986S variant using PCR-RFLP method.
No significant difference was observed for the A986S variant of 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/m) and overweight/obese (BMI ≥ 25kg/m) subjects.
Our findings do not support a role for effect of the 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.
关于钙对结直肠癌(CRC)的影响,并考虑到钙敏感受体(CaSR)在钙稳态中的关键作用,本研究调查了基因rs1801725或A986S变体是否与CRC风险易感性相关。
本研究作为病例对照研究进行,纳入了303例CRC患者和354例对照。使用PCR-RFLP方法对所有657名受试者的基因A986S变体进行基因分型。
在病例组和对照组之间,基因的A986S变体在基因型或等位基因频率上均未观察到显著差异,即使在调整年龄、BMI、性别、吸烟状况和CRC家族史后,这种差异仍然不显著。也未观察到BMI、性别或肿瘤部位对A986S变体与CRC关联的效应修饰证据。此外,分别分析了对照组和病例组中与A986S变体相关的肥胖风险,我们观察到正常体重(BMI<25kg/m)和超重/肥胖(BMI≥25kg/m)受试者之间无显著差异。
我们的研究结果不支持基因A986S变体对CRC风险有影响的作用;然而,这一发现需要证实,该基因变体在致癌过程中的作用需要进一步研究。