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鉴定早期结直肠癌中的潜在 DNA 甲基化标志物。

Identifying potential DNA methylation markers in early-stage colorectal Cancer.

机构信息

Department of Pathology, School of Basic Medical Science, Southern Medical University, Guangzhou, 510515, China.

AnchorDx Medical Co., Ltd, Unit 502, 3(rd) Luoxuan Road, International Bio-Island, Guangzhou, 510300, China.

出版信息

Genomics. 2020 Sep;112(5):3365-3373. doi: 10.1016/j.ygeno.2020.06.007. Epub 2020 Jun 10.

Abstract

Colorectal cancer (CRC) is the second leading malignancy worldwide. Accurate screening is pivotal to early CRC detection, yet current screening modality involves invasive colonoscopy while non-invasive FIT tests have limited sensitivity. We applied a DNA methylation assay to identify biomarkers for early-stage CRC detection, risk stratification and precancerous lesion screening at tissue level. A model of biomarkers SFMBT2, ITGA4, THBD and ZNF304 showed 96.1% sensitivity and 87.0% specificity in CRC detection, with 100.0% sensitivity for advanced precancerous lesion and stage I CRC. Performances were further validated with TCGA data set, which showed a consistent AUC of 0.99 and exhibited specificity against other cancer types. KCNJ12, VAV3-AS1 and EVC were further identified for stage stratification (stage 0-I versus stage II-IV), with AUC of 0.87, 83.0% sensitivity and 71.2% specificity. Additionally, dual markers of NEUROD1 and FAM72C showed 83.2% sensitivity and 77.4% specificity in differing non-advanced precancerous lesions from inflammatory bowel diseases.

摘要

结直肠癌(CRC)是全球第二大恶性肿瘤。准确的筛查对于早期 CRC 的检测至关重要,但目前的筛查方法涉及侵入性结肠镜检查,而非侵入性 FIT 检查敏感性有限。我们应用 DNA 甲基化分析来鉴定组织水平早期 CRC 检测、风险分层和癌前病变筛查的生物标志物。SFMBT2、ITGA4、THBD 和 ZNF304 的生物标志物模型在 CRC 检测中显示出 96.1%的敏感性和 87.0%的特异性,对高级别癌前病变和 I 期 CRC 的敏感性为 100.0%。这些性能在 TCGA 数据集上得到了进一步验证,AUC 一致为 0.99,并表现出对其他癌症类型的特异性。进一步鉴定了 KCNJ12、VAV3-AS1 和 EVC 用于分期分层(0-I 期与 II-IV 期),AUC 为 0.87,敏感性为 83.0%,特异性为 71.2%。此外,NEUROD1 和 FAM72C 的双重标志物在炎症性肠病的不同非高级别癌前病变中显示出 83.2%的敏感性和 77.4%的特异性。

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