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

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...

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Detalles Bibliográficos
Autores principales: Lee, Min Kyung, Brown, Meredith S, Wilkins, Owen M, Pattabiraman, Diwakar R, Christensen, Brock C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118069/
https://www.ncbi.nlm.nih.gov/pubmed/35382559
http://dx.doi.org/10.2217/epi-2022-0023
Descripción
Sumario: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.