Faculty of Biology and Biotechnology, University of Warmia and Mazury, 10-719 Olsztyn, Poland.
Faculty of Medicine, Collegium Medicum, University of Warmia and Mazury, 10-082 Olsztyn, Poland.
Nutrients. 2020 Apr 3;12(4):998. doi: 10.3390/nu12040998.
Colorectal cancer (CRC) is the third most commonly occurring cancer worldwide. Intestinal cells are gene expression sites and, as a consequence, they are capable of converting pro-vitamin D into the active paracrine and autocrine forms. It was demonstrated that rs10877012 polymorphism in the gene influenced the circulating vitamin D level. This provided a rationale for determining the role that this polymorphism plays in the risk of developing colon cancer. In this study, we investigated the association of rs10877012 (T/G) polymorphism in the gene with CRC susceptibility. The study population ( = 325) included CRC patients ( = 106) and healthy controls ( = 219). DNA was extracted from peripheral leukocytes and analyzed for the polymorphism using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. We found an association between the presence of the T allele at the polymorphic site (odds ratio (OR) = 2.94; 95% CI 1.77-4.86; < 0.0001) and a decreased CRC incidence.
结直肠癌(CRC)是全球第三大常见癌症。肠道细胞是基因表达的场所,因此它们能够将前维生素 D 转化为有活性的旁分泌和自分泌形式。已经证明基因中的 rs10877012 多态性影响循环维生素 D 水平。这为确定这种多态性在结肠癌发病风险中的作用提供了依据。在这项研究中,我们研究了基因中的 rs10877012(T/G)多态性与 CRC 易感性的关系。研究人群(=325)包括 CRC 患者(=106)和健康对照(=219)。从外周白细胞中提取 DNA,并使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法分析基因中的多态性。我们发现多态性位点 T 等位基因的存在与 CRC 发病率降低之间存在关联(比值比(OR)=2.94;95%置信区间 1.77-4.86;<0.0001)。