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

Author:

Bramblet Rachel M.1ORCID,Bakkum-Gamez Jamie N.1ORCID,Slettedahl Seth W.2ORCID,Foote Patrick H.3ORCID,Taylor William R.3ORCID,Berger Calise K.3ORCID,Gysbers Brianna J.3ORCID,Arndt Jacquelyn3ORCID,Chen Longwen4ORCID,Doering Karen A.3ORCID,Burger Kelli N.2ORCID,Mahoney Douglas W.2ORCID,Sherman Mark E.5ORCID,Kisiel John B.3ORCID,Samadder N. Jewel6ORCID

Affiliation:

1. 1Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, Minnesota.

2. 2Department of Quantitative Health Sciences, Mayo Clinic Rochester, Minnesota.

3. 3Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.

4. 4Division of Anatomic Pathology, Mayo Clinic, Scottsdale, Arizona.

5. 5Department of Quantitative Health Sciences, Mayo Clinic, Jacksonville, Florida.

6. 6Department of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona.

Abstract

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.

Funder

Gerstner Family Foundation

Center for Individualized Medicine, Mayo Clinic

National Cancer Institute

V Foundation for Cancer Research

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

Reference39 articles.

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