Novel methylated DNA markers accurately discriminate Lynch syndrome associated colorectal neoplasia

Author:

Ballester Veroushka1ORCID,Taylor William R2,Slettedahl Seth W3ORCID,Mahoney Douglas W3,Yab Tracy C2ORCID,Sinicrope Frank A2ORCID,Boland Clement R4ORCID,Lidgard Graham P5,Cruz-Correa Marcia R6,Smyrk Thomas C7ORCID,Boardman Lisa A2ORCID,Ahlquist David A2,Kisiel John B2ORCID

Affiliation:

1. Division of Digestive & Liver Diseases, Columbia University, New York,    NY 10032, USA

2. Division of Gastroenterology & Hepatology, Mayo Clinic, Rochester, MN 55905, USA

3. Biostatistics & Informatics, Mayo Clinic, Rochester, MN 55905, USA

4. Division of Gastroenterology, UCSD, San Diego, CA 92093, USA

5. Exact Sciences, Madison, WI 53719, USA

6. Comprehensive Cancer Center, University of Puerto Rico Medical Sciences Campus, San Juan, PR 00936, USA

7. Department of Laboratory Medicine & Pathology, Mayo Clinic, Rochester, MN 55905, USA

Abstract

Aim: 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. Patients & methods: 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. Results: OPLAH was the most discriminant MDM with areas under the receiver operating characteristic curve ≥0.97 for colorectal neoplasia in LS and sporadic tissues. ALKBH5, was uniquely hypermethylated in LS neoplasms. Conclusion: Highly discriminant MDMs for colorectal neoplasia in LS were identified with potential use in screening and surveillance.

Funder

Hispanic Clinical and Translational Research Education and Career Development

The Clinical Core of the Mayo Clinic for Cell Signaling in Gastroenterology

Exact Sciences

Additional support was provided to John Kisiel

Mayo Foundation for Medical Education and Research

Eugene and Eva Lane

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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