Methylated DNA Markers for Sporadic Colorectal and Endometrial Cancer Are Strongly Associated with Lynch Syndrome Cancers.

Rachel M Bramblet, Jamie N Bakkum-Gamez, Seth W Slettedahl, Patrick H Foote, William R Taylor, Calise K Berger, Brianna J Gysbers, Jacquelyn Arndt, Longwen Chen, Karen A Doering, Kelli N Burger, Douglas W Mahoney, Mark E Sherman, John B Kisiel, N Jewel Samadder
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Abstract

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.

Prevention relevance: 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.

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散发性结直肠癌和子宫内膜癌症的甲基化DNA标记物与林奇综合征癌症密切相关。
林奇综合征(LS)显著增加结直肠癌和子宫内膜癌的风险。LS癌的早期检测生物标志物可以减少对侵入性筛查和外科预防的需求。为了验证先前在散发性结直肠癌癌症和癌症子宫内膜癌中鉴定的一组甲基化DNA标记物(MDM)在LS中对这些癌症的区分。在病例对照设计中,通过组织提取DNA上的qMSP测定先前鉴定的用于检测结直肠癌癌症和癌症子宫内膜癌的MDM。将结果标准化为每个样本中的ACTB值。在散发病例和对照中训练用于分类结直肠癌癌症和子宫内膜癌症的最小绝对收缩和选择算子模型,然后应用于分类结直肠癌癌症和子宫内膜癌症、LS患者和交叉验证,子宫内膜癌症病例(30 LS,48散发)和子宫内膜对照(29 LS,37散发)。3-MDM小组(LASS4、LRRC4和PPP2R5C)将LS-CRC从LS对照中分类,AUC为0.92(0.84-0.99);散发性癌症的结果相似。6-MDM组(SFMBT2、MPZ、CYTH2、DIDO1、chr10.4479和EMX2OS)以0.92(0.83-1.0)的AUC区分LS-EC和LS对照;散发性子宫内膜癌症与散发性对照组的AUC名义上更高,为0.99(0.96-1.0)。先前在散发性癌症和癌症中鉴定的MDM区分了LS中的子宫内膜癌症和良性子宫内膜以及结直肠癌癌症和良性结直肠。这支持将LS患者纳入未来评估子宫内膜癌症和癌症MDMs的前瞻性临床试验,并可能为这一高危人群的癌症筛查或监测提供新的途径。预防相关性:林奇综合征(LS)显著增加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症和结直肠癌癌症中鉴定的甲基化DNA标记物区分LS中的良性和癌症组织。
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