| Literature DB >> 33396258 |
Nam-Yun Cho1, Ji-Won Park2, Xianyu Wen3, Yun-Joo Shin1, Jun-Kyu Kang4, Sang-Hyun Song4, Hwang-Phill Kim4, Tae-You Kim4,5, Jeong Mo Bae1,6, Gyeong Hoon Kang1,6.
Abstract
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 (ADGRB1, ANKRD13, FAM123A, GLI3, PCDHG, PPP1R16B, SLIT3, and TMEM90B) and developed a five-marker panel (FAM123A, GLI3, PPP1R16B, SLIT3, and TMEM90B) 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 (n = 117) and healthy volunteers (n = 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.Entities:
Keywords: MethyLight; cfDNA; colorectal cancer; droplet digital PCR; methylation; plasma
Year: 2020 PMID: 33396258 PMCID: PMC7823774 DOI: 10.3390/diagnostics11010051
Source DB: PubMed Journal: Diagnostics (Basel) ISSN: 2075-4418