Division of Digestive & Liver Diseases, Columbia University, New York, NY 10032, USA.
Division of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN 55905, USA.
Epigenomics. 2020 Dec;12(24):2173-2187. doi: 10.2217/epi-2020-0132. Epub 2020 Dec 22.
Acquired molecular changes in Lynch syndrome (LS) colorectal tumors have been largely unstudied. We identified methylated DNA markers (MDMs) for discrimination of colorectal neoplasia in LS and determined if these MDMs were comparably discriminant in sporadic patients. For LS discovery, we evaluated DNA from 53 colorectal case and control tissues using next generation sequencing. For validation, blinded methylation-specific PCR assays to the selected MDMs were performed on 197 cases and controls. was the most discriminant MDM with areas under the receiver operating characteristic curve ≥0.97 for colorectal neoplasia in LS and sporadic tissues. , was uniquely hypermethylated in LS neoplasms. Highly discriminant MDMs for colorectal neoplasia in LS were identified with potential use in screening and surveillance.
林奇综合征(LS)结直肠肿瘤中获得的分子变化在很大程度上尚未得到研究。我们鉴定了用于区分 LS 结直肠肿瘤的甲基化 DNA 标志物(MDM),并确定这些 MDM 在散发性患者中是否具有类似的区分能力。为了发现 LS,我们使用下一代测序评估了 53 例结直肠病例和对照组织中的 DNA。为了验证,我们对 197 例病例和对照进行了针对选定 MDM 的甲基化特异性 PCR 检测。在 LS 和散发性组织中,是最具区分能力的 MDM,其受试者工作特征曲线下面积≥0.97。在 LS 肿瘤中,和是唯一高度甲基化的。我们鉴定了用于 LS 结直肠肿瘤的高度区分 MDM,它们具有用于筛查和监测的潜在用途。