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Correlation of MLH1 and MGMT methylation levels between peripheral blood leukocytes and colorectal tissue DNA samples in colorectal cancer patients

机译:大肠癌患者外周血白细胞与大肠组织DNA样本之间MLH1和MGMT甲基化水平的相关性

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摘要

CpG island methylation in the promoter regions of the DNA mismatch repair gene mutator L homologue 1 (MLH1) and DNA repair gene O6-methylguanine-DNA methyltransferase (MGMT) genes has been shown to occur in the leukocytes of peripheral blood and colorectal tissue. However, it is unclear whether the methylation levels in the blood leukocytes and colorectal tissue are correlated. The present study analyzed and compared the levels of MGMT and MLH1 gene methylation in the leukocytes of peripheral blood and colorectal tissues obtained from patients with colorectal cancer (CRC). The methylation levels of MGMT and MLH1 were examined using methylation-sensitive high-resolution melting (MS-HRM) analysis. A total of 44 patients with CRC were selected based on the MLH1 and MGMT gene methylation levels in the leukocytes of the peripheral blood. Corresponding colorectal tumor and normal tissues were obtained from each patient and the DNA methylation levels were determined. The correlation coefficients were evaluated using Spearman’s rank test. Agreement was determined by generalized κ-statistics. Spearman’s rank correlation coefficients (r) for the methylation levels of the MGMT and MLH1 genes in the leukocytes of the peripheral blood and normal colorectal tissue were 0.475 and 0.362, respectively (P=0.001 and 0.016, respectively). The agreement of the MGMT and MLH1 gene methylation levels in the leukocytes of the peripheral blood and normal colorectal tissue were graded as fair and poor (κ=0.299 and 0.126, respectively). The methylation levels of MGMT and MLH1 were moderately and weakly correlated between the patient-matched leukocytes and the normal colorectal tissue, respectively. Blood-derived DNA methylation measurements may not always represent the levels of normal colorectal tissue methylation.
机译:DNA错配修复基因突变体L同源物1(MLH1)和DNA修复基因O 6 -甲基鸟嘌呤-DNA甲基转移酶(MGMT)基因的启动子区域的CpG岛甲基化已显示在白细胞中。外周血和结直肠组织。但是,尚不清楚血白细胞和结直肠组织中的甲基化水平是否相关。本研究分析并比较了来自结直肠癌(CRC)患者的外周血和结直肠组织白细胞中MGMT和MLH1基因甲基化的水平。使用甲基化敏感的高分辨率熔解(MS-HRM)分析检查了MGMT和MLH1的甲基化水平。根据外周血白细胞中的MLH1和MGMT基因甲基化水平,选择了44例CRC患者。从每位患者获得相应的结肠直肠肿瘤和正常组织,并测定DNA甲基化水平。相关系数使用Spearman等级检验进行了评估。一致性由广义κ统计量确定。外周血和正常结直肠组织白细胞中MGMT和MLH1基因的甲基化水平的Spearman等级相关系数(r)分别为0.475和0.362(分别为P = 0.001和0.016)。外周血和正常结直肠组织白细胞中MGMT和MLH1基因甲基化水平的一致性分为公平和不良(分别为κ= 0.299和0.126)。在患者匹配的白细胞和正常结直肠组织之间,MGMT和MLH1的甲基化水平分别为中度和弱度相关。血液来源的DNA甲基化测量值可能并不总是代表正常结直肠组织甲基化的水平。

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