High-resolution Nanopore methylome-maps reveal random hyper-methylation at CpG-poor regions as driver of chemoresistance in leukemias.


Journal

Communications biology
ISSN: 2399-3642
Titre abrégé: Commun Biol
Pays: England
ID NLM: 101719179

Informations de publication

Date de publication:
08 04 2023
Historique:
received: 15 11 2022
accepted: 24 03 2023
medline: 11 4 2023
entrez: 8 4 2023
pubmed: 9 4 2023
Statut: epublish

Résumé

Aberrant DNA methylation at CpG dinucleotides is a cancer hallmark that is associated with the emergence of resistance to anti cancer treatment, though molecular mechanisms and biological significance remain elusive. Genome scale methylation maps by currently used methods are based on chemical modification of DNA and are best suited for analyses of methylation at CpG rich regions (CpG islands). We report the first high coverage whole-genome map in cancer using the long read nanopore technology, which allows simultaneous DNA-sequence and -methylation analyses on native DNA. We analyzed clonal epigenomic/genomic evolution in Acute Myeloid Leukemias (AMLs) at diagnosis and relapse, after chemotherapy. Long read sequencing coupled to a novel computational method allowed definition of differential methylation at unprecedented resolution, and showed that the relapse methylome is characterized by hypermethylation at both CpG islands and sparse CpGs regions. Most differentially methylated genes, however, were not differentially expressed nor enriched for chemoresistance genes. A small fraction of under-expressed and hyper-methylated genes at sparse CpGs, in the gene body, was significantly enriched in transcription factors (TFs). Remarkably, these few TFs supported large gene-regulatory networks including 50% of all differentially expressed genes in the relapsed AMLs and highly-enriched in chemoresistance genes. Notably, hypermethylated regions at sparse CpGs were poorly conserved in the relapsed AMLs, under-represented at their genomic positions and showed higher methylation entropy, as compared to CpG islands. Analyses of available datasets confirmed TF binding to their target genes and conservation of the same gene-regulatory networks in large patient cohorts. Relapsed AMLs carried few patient specific structural variants and DNA mutations, apparently not involved in drug resistance. Thus, drug resistance in AMLs can be mainly ascribed to the selection of random epigenetic alterations at sparse CpGs of a few transcription factors, which then induce reprogramming of the relapsing phenotype, independently of clonal genomic evolution.

Identifiants

pubmed: 37031307
doi: 10.1038/s42003-023-04756-8
pii: 10.1038/s42003-023-04756-8
pmc: PMC10082806
doi:

Substances chimiques

DNA 9007-49-2
Transcription Factors 0
Antineoplastic Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

382

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2023. The Author(s).

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Auteurs

Alberto Magi (A)

Department of Information Engineering, University of Florence, Florence, Italy. albertomagi@gmail.com.
Institute for Biomedical Technologies, National Research Council, Segrate, Milano, Italy. albertomagi@gmail.com.

Gianluca Mattei (G)

Department of Information Engineering, University of Florence, Florence, Italy.

Alessandra Mingrino (A)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Chiara Caprioli (C)

Department of Experimental Oncology, IEO European Institute of Oncology IRCCS, Milano, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.

Chiara Ronchini (C)

Department of Experimental Oncology, IEO European Institute of Oncology IRCCS, Milano, Italy.

Gianmaria Frigè (G)

Department of Experimental Oncology, IEO European Institute of Oncology IRCCS, Milano, Italy.

Roberto Semeraro (R)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Davide Bolognini (D)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Alessandro Rambaldi (A)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Azienda Socio-Sanitaria Territoriale Papa Giovanni XXIII, Bergamo, Italy.

Anna Candoni (A)

Clinica Ematologica, Azienda Sanitaria Universitaria Integrata di Udine, Udine, Italy.

Emanuela Colombo (E)

Department of Experimental Oncology, IEO European Institute of Oncology IRCCS, Milano, Italy.

Luca Mazzarella (L)

Department of Experimental Oncology, IEO European Institute of Oncology IRCCS, Milano, Italy.

Pier Giuseppe Pelicci (PG)

Department of Experimental Oncology, IEO European Institute of Oncology IRCCS, Milano, Italy. piergiuseppe.pelicci@ieo.it.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy. piergiuseppe.pelicci@ieo.it.

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