Chen Zhiliang, Zhao Guodong, Wang Kai, Wang Xiaomei, Ma Yong, Xiong Shangmin, Zheng Minxue, Fei Sujuan
Department of Gastroenterology, Affiliated Hospital of Xuzhou Medical University, Xuzhou Jiangsu 221002, China.
Institute of Digestive Diseases, Xuzhou Medical University, Xuzhou Jiangsu 221002, China.
J Cancer. 2021 Apr 30;12(12):3678-3685. doi: 10.7150/jca.57114. eCollection 2021.
: A number of plasma methylated DNA biomarkers related to colorectal cancer (CRC) have been identified. However, the effect of methylation level in leukocytes on plasma-based methylation test was rarely reported. : Blood samples from 213 individuals including 91 CRC patients were collected and separated into 3.5 mL of plasma and paired leukocyte fractions. DNA were extracted from plasma and leukocytes and bisulfite converted, followed by ColoDefense test that detects methylated (m) and methylated (m) simultaneously in a single qPCR reaction. : Both m and m levels in leukocytes exhibited no significant difference among CRC, benign tumors and healthy controls. However, m and m levels in plasma were significantly higher in CRC group than those in other groups. The sensitivities of m and m alone for detecting CRC with plasma samples were 75.8% and 60.4% with specificities of 94.7% and 86.8%, respectively. These two markers in combination exhibited an improved sensitivity of 85.7% for CRC detection with a specificity of 86.8%, mostly attributable to increased sensitivity of 81.8% for detecting stage 0-II CRC. AUC values for m and m alone were 0.864 (95% CI: 0.798 - 0.929) and 0.796 (95% CI: 0.719 - 0.874), respectively, but improved to 0.972 (95% CI: 0.949 - 0.996) when combined for ColoDefense test. : The leukocytes gDNA will not affect the performance of plasma ColoDefense test, and plasma ColoDefense test exhibited high sensitivity and specificity in a validation set, demonstrating its potential as a non-invasive and cost-effective method for CRC early detection.
已鉴定出一些与结直肠癌(CRC)相关的血浆甲基化DNA生物标志物。然而,白细胞甲基化水平对基于血浆的甲基化检测的影响鲜有报道。收集了包括91例CRC患者在内的213名个体的血样,并将其分离为3.5 mL血浆和配对的白细胞组分。从血浆和白细胞中提取DNA并进行亚硫酸氢盐转化,然后进行ColoDefense检测,该检测可在单个qPCR反应中同时检测甲基化的(m)和甲基化的(m)。白细胞中的m和m水平在CRC、良性肿瘤和健康对照之间均无显著差异。然而,CRC组血浆中的m和m水平显著高于其他组。仅用血浆样本检测CRC时,m和m的敏感性分别为75.8%和60.4%,特异性分别为94.7%和86.8%。这两种标志物联合使用时,对CRC检测的敏感性提高到85.7%,特异性为86.8%,这主要归因于检测0-II期CRC时敏感性提高了81.8%。m和m单独使用时的AUC值分别为0.864(95%CI:0.798 - 0.929)和0.796(95%CI:0.719 - 0.874),但在ColoDefense检测联合使用时提高到0.972(95%CI:0.949 - 0.996)。白细胞基因组DNA不会影响血浆ColoDefense检测的性能,并且血浆ColoDefense检测在验证集中表现出高敏感性和特异性,证明了其作为CRC早期检测的非侵入性和成本效益高的方法的潜力。