Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota.
Department of Quantitative Health Sciences, Mayo Clinic Rochester, Minnesota.
Cancer Prev Res (Phila). 2023 Nov 1;16(11):611-620. doi: 10.1158/1940-6207.CAPR-23-0107.
Lynch syndrome (LS) markedly increases risks of colorectal and endometrial cancers. Early detection biomarkers for LS cancers could reduce the needs for invasive screening and surgical prophylaxis.To validate a panel of methylated DNA markers (MDM) previously identified in sporadic colorectal cancer and endometrial cancer for discrimination of these cancers in LS.In a case-control design, previously identified MDMs for the detection of colorectal cancer and endometrial cancer were assayed by qMSP on tissue-extracted DNA. Results were normalized to ACTB values within each sample. Least absolute shrinkage and selection operator models to classify colorectal cancer and endometrial cancer were trained on sporadic cases and controls and then applied to classify colorectal cancer and endometrial cancer, in those with LS, and cross-validated.We identified colorectal cancer cases (23 with LS, 48 sporadic), colorectal controls (32 LS, 48 sporadic), endometrial cancer cases (30 LS, 48 sporadic), and endometrial controls (29 LS, 37 sporadic). A 3-MDM panel (LASS4, LRRC4, and PPP2R5C) classified LS-CRC from LS controls with an AUC of 0.92 (0.84-0.99); results were similar for sporadic colorectal cancer. A 6-MDM panel (SFMBT2, MPZ, CYTH2, DIDO1, chr10.4479, and EMX2OS) discriminated LS-EC from LS controls with an AUC of 0.92 (0.83-1.0); the AUC for sporadic endometrial cancer versus sporadic controls was nominally higher, 0.99 (0.96-1.0).MDMs previously identified in sporadic endometrial cancer and colorectal cancer discriminate between endometrial cancer and benign endometrium and colorectal cancer and benign colorectum in LS. This supports the inclusion of patients with LS within future prospective clinical trials evaluating endometrial cancer and colorectal cancer MDMs and may provide a new avenue for cancer screening or surveillance in this high-risk population.
Lynch syndrome (LS) markedly increases risks of colorectal and endometrial cancers. Early detection biomarkers for LS cancers could reduce the needs for invasive screening and surgery. Methylated DNA markers previously identified in sporadic endometrial cancer and colorectal cancer discriminate between benign and cancer tissue in LS.
林奇综合征(LS)显著增加了结直肠癌和子宫内膜癌的风险。LS 癌症的早期检测生物标志物可以减少对侵入性筛查和手术预防的需求。为了验证先前在散发性结直肠癌和子宫内膜癌中发现的一组甲基化 DNA 标志物(MDM)是否可用于区分 LS 癌症。在病例对照设计中,通过 qMSP 对组织提取的 DNA 进行了先前鉴定的用于检测结直肠癌和子宫内膜癌的 MDM 检测。结果在每个样本内均与 ACTB 值进行了归一化。使用最小绝对收缩和选择算子模型对散发性病例和对照进行分类,并应用于 LS 中结直肠癌和子宫内膜癌的分类,并进行交叉验证。我们鉴定了结直肠癌病例(23 例 LS,48 例散发性),结直肠对照(32 例 LS,48 例散发性),子宫内膜癌病例(30 例 LS,48 例散发性)和子宫内膜对照(29 例 LS,37 例散发性)。一个 3-MDM 面板(LASS4、LRRC4 和 PPP2R5C)将 LS-CRC 与 LS 对照的 AUC 为 0.92(0.84-0.99)进行分类;散发性结直肠癌的结果相似。一个 6-MDM 面板(SFMBT2、MPZ、CYTH2、DIDO1、chr10.4479 和 EMX2OS)将 LS-EC 与 LS 对照的 AUC 为 0.92(0.83-1.0)进行分类;散发性子宫内膜癌与散发性对照的 AUC 略高,为 0.99(0.96-1.0)。先前在散发性子宫内膜癌和结直肠癌中鉴定的 MDM 可区分 LS 中子宫内膜癌与良性子宫内膜癌和结直肠癌与良性结直肠。这支持在未来评估 LS 中子宫内膜癌和结直肠癌 MDM 的前瞻性临床试验中纳入 LS 患者,并可能为高危人群的癌症筛查或监测提供新途径。
林奇综合征(LS)显著增加了结直肠癌和子宫内膜癌的风险。LS 癌症的早期检测生物标志物可以减少对侵入性筛查和手术的需求。先前在散发性子宫内膜癌和结直肠癌中鉴定的甲基化 DNA 标志物可区分 LS 中的良性和癌症组织。