Cho Nam-Yun, Park Ji-Won, Wen Xianyu, Shin Yun-Joo, Kang Jun-Kyu, Song Sang-Hyun, Kim Hwang-Phill, Kim Tae-You, Bae Jeong Mo, Kang Gyeong Hoon
Laboratory of Epigenetics, Cancer Research Institute, Seoul National University College of Medicine, Seoul 03080, Korea.
Department of General Surgery, Seoul National University College of Medicine, Seoul 03030, Korea.
Diagnostics (Basel). 2020 Dec 31;11(1):51. doi: 10.3390/diagnostics11010051.
Cancer tissues have characteristic DNA methylation profiles compared with their corresponding normal tissues that can be utilized for cancer diagnosis with liquid biopsy. Using a genome-scale DNA methylation approach, we sought to identify a panel of DNA methylation markers specific for cell-free DNA (cfDNA) from patients with colorectal cancer (CRC). By comparing DNA methylomes between CRC and normal mucosal tissues or blood leukocytes, we identified eight cancer-specific methylated loci (, , , , , , , and ) and developed a five-marker panel (, , , , and ) that detected CRC in liquid biopsies with a high sensitivity and specificity with a droplet digital MethyLight assay. In a set of cfDNA samples from CRC patients ( = 117) and healthy volunteers ( = 60), a panel of five markers on the platform of the droplet digital MethyLight assay detected stages I-III and stage IV CRCs with sensitivities of 45.9% and 95.7%, respectively, and a specificity of 95.0%. The number of detected markers was correlated with the cancer stage, perineural invasion, lymphatic emboli, and venous invasion. Our five-marker panel with the droplet digital MethyLight assay showed a high sensitivity and specificity for the detection of CRC with cfDNA samples from patients with metastatic CRC.
与相应的正常组织相比,癌组织具有特征性的DNA甲基化谱,可用于液体活检进行癌症诊断。我们采用全基因组规模的DNA甲基化方法,试图鉴定一组针对结直肠癌(CRC)患者游离DNA(cfDNA)的DNA甲基化标志物。通过比较CRC与正常黏膜组织或血液白细胞之间的DNA甲基化组,我们鉴定出8个癌症特异性甲基化位点(、、、、、、和),并开发了一个五标志物组合(、、、、和),该组合通过液滴数字甲基化荧光定量分析在液体活检中检测CRC时具有高灵敏度和特异性。在一组来自CRC患者(n = 117)和健康志愿者(n = 60)的cfDNA样本中,液滴数字甲基化荧光定量分析平台上的五标志物组合检测I - III期和IV期CRC的灵敏度分别为45.9%和95.7%,特异性为95.0%。检测到的标志物数量与癌症分期、神经周围浸润、淋巴栓子和静脉浸润相关。我们的五标志物组合与液滴数字甲基化荧光定量分析对来自转移性CRC患者的cfDNA样本检测CRC显示出高灵敏度和特异性。