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Functional polymorphisms in CD166/ALCAM gene associated with increased risk for breast cancer in a Chinese population

机译:CD166 / ALCAM基因的功能多态性与中国人群患乳腺癌的风险增加相关

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Activated Leukocyte Cell Adhesion Molecules (ALCAM, also called CD166, MEMD) are cell surface immunoglobulins that are considered to be prognostic markers for breast cancer. CD166/ALCAM has gained increasing attention because of its significant association with tumor progression and the metastatic spread of breast cancer. Two polymorphisms have been identified in the CD166/ALCAM gene: 5′UTR C/T (rs6437585) and 3′UTR A/G (rs11559013). We analyzed the genotypes of 1033 individuals with breast cancer, and 1116 controls; odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using logistic regression. The effects and functions of polymorphisms were examined using luciferase gene expression assays and real-time PCR analyses. Our data demonstrated that individuals with the rs6437585 CT + TT genotype had an OR of 1.38 (95% CI, 1.11–1.72) for developing breast cancer, compared to those with the CC genotype. The T allele increased the risk of breast cancer in a dose-dependent manner (P trend < 0.001). However, there were no significant differences found between cases and controls at the rs11559013 A/G site. Additional experiments that we performed, which focused on reporter gene expression driven by CD166/ALCAM promoters, demonstrated that the presence of an rs6437585 T allele led to greater transcriptional activity than the rs6437585 C allele. This was consistent with the increased cancer risk that we observed in our case–control analysis.
机译:活化白细胞粘附分子(ALCAM,也称为CD166,MEMD)是细胞表面免疫球蛋白,被认为是乳腺癌的预后标志物。由于CD166 / ALCAM与肿瘤的进展和乳腺癌的转移扩散密切相关,因此受到越来越多的关注。已在CD166 / ALCAM基因中鉴定出两个多态性:5'UTR C / T(rs6437585)和3'UTR A / G(rs11559013)。我们分析了1033例乳腺癌患者和1116例对照的基因型。使用逻辑回归估计比值比(OR)和95%置信区间(CI)。使用荧光素酶基因表达测定和实时PCR分析检查了多态性的作用和功能。我们的数据表明,与CC基因型相比,具有rs6437585 CT + TT基因型的个体患乳腺癌的OR为1.38(95%CI,1.11-1.72)。 T等位基因以剂量依赖性方式增加患乳腺癌的风险(P trend <0.001)。但是,rs11559013 A / G站点的病例与对照之间没有发现显着差异。我们进行的其他实验侧重于由CD166 / ALCAM启动子驱动的报告基因表达,证明rs6437585 T等位基因的存在导致比rs6437585 C等位基因更大的转录活性。这与我们在病例对照分析中观察到的癌症风险增加一致。

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