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Colorectal cancer progression to metastasis is associated with dynamic genome-wide biphasic 5-hydroxymethylcytosine accumulation

Murcott, Ben; Honig, Floris; Halliwell, Dominic Oliver; Tian, Yuan; Robson, James Lawrence; Manasterski, Piotr; Pinnell, Jennifer; Dix-Peek, Thérèse; Uribe-Lewis, Santiago; Ibrahim, Ashraf E. K.; Sero, Julia; Gurevich, David; Nikolaou, Nikolas; Murrell, Adele

Colorectal cancer progression to metastasis is associated with dynamic genome-wide biphasic 5-hydroxymethylcytosine accumulation Thumbnail


Authors

Ben Murcott

Floris Honig

Dominic Oliver Halliwell

Yuan Tian

James Lawrence Robson

Piotr Manasterski

Jennifer Pinnell

Thérèse Dix-Peek

Santiago Uribe-Lewis

Ashraf E. K. Ibrahim

Julia Sero

David Gurevich

Nikolas Nikolaou

Adele Murrell



Abstract

Background: Colorectal cancer (CRC) progression from adenoma to adenocarcinoma is associated with global reduction in 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC). DNA hypomethylation continues upon liver metastasis. Here we examine 5hmC changes upon progression to liver metastasis. Results: 5hmC is increased in metastatic liver tissue relative to the primary colon tumour and expression of TET2 and TET3 is negatively correlated with risk for metastasis in patients with CRC. Genes associated with increased 5-hydroxymethylcytosine show KEGG enrichment for adherens junctions, cytoskeleton and cell migration around a core cadherin (CDH2) network. Overall, the 5-hydroxymethylcyosine profile in the liver metastasis is similar to normal colon appearing to recover at many loci where it was originally present in normal colon and then spreading to adjacent sites. The underlying sequences at the recover and spread regions are enriched for SALL4, ZNF770, ZNF121 and PAX5 transcription factor binding sites. Finally, we show in a zebrafish migration assay using SW480 CRISPR-engineered TET knockout and rescue cells that reduced TET expression leads to a reduced migration frequency. Conclusions: Together these results suggest a biphasic trajectory for 5-hydroxymethyation dynamics that has bearing on potential therapeutic interventions aimed at manipulating 5-hydroxymethylcytosine levels.

Journal Article Type Article
Acceptance Date Apr 3, 2025
Online Publication Date Apr 16, 2025
Publication Date Apr 16, 2025
Deposit Date Apr 28, 2025
Publicly Available Date Apr 29, 2025
Journal BMC Biology
Electronic ISSN 1741-7007
Publisher BioMed Central
Peer Reviewed Peer Reviewed
Volume 23
Issue 1
Article Number 100
DOI https://doi.org/10.1186/s12915-025-02205-y
Keywords 5-Hydroxymethylcytosine, Epigenetics, Ten-eleven-translocation (TET), Colorectal cancer progression to metastasis, Zebrafish assay
Public URL https://uwe-repository.worktribe.com/output/14319390

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