Distinct cytosine modification profiles define epithelial-to-mesenchymal cell-state transitions

Author:

Lee Min Kyung1ORCID,Brown Meredith S2,Wilkins Owen M3ORCID,Pattabiraman Diwakar R2ORCID,Christensen Brock C124ORCID

Affiliation:

1. Department of Epidemiology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756, USA

2. Department of Molecular & Systems Biology, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756, USA

3. Norris Cotton Cancer Center, Dartmouth-Hitchcock Medical Center, Lebanon, NH 03756, USA

4. Department of Community & Family Medicine, Geisel School of Medicine at Dartmouth, Lebanon, NH 03756, USA

Abstract

Background: Epithelial-to-mesenchymal transition (EMT) is an early step in the invasion-metastasis cascade, involving progression through intermediate cell states. Due to challenges with isolating intermediate cell states, genome-wide cytosine modifications that define transition are not completely understood. Methods: The authors measured multiple DNA cytosine modification marks and chromatin accessibility across clonal populations residing in specific EMT states. Results: Clones exhibiting more intermediate EMT phenotypes demonstrated increased 5-hydroxymethylcytosine and decreased 5-methylcytosine. Open chromatin regions containing increased 5-hydroxymethylcytosine CpG loci were enriched in EMT transcription factor motifs and were associated with Rho GTPases. Conclusion: The results indicate the importance of both distinct and shared epigenetic profiles associated with EMT processes that may be targeted to prevent EMT progression.

Funder

National Institutes of Health

National Cancer Institute

Geisel School of Medicine at Dartmouth (The Elmer R. Pfefferkorn & Allan U. Munck Education and Research Fund Friends of the Norris Cotton Cancer Center

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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