DNA Methylation and Bladder Cancer: Where Genotype does not Predict Phenotype.

Bladder cancer DNA methylation cancer biomarkers epigenetic genotype phenotype

Journal

Current genomics
ISSN: 1389-2029
Titre abrégé: Curr Genomics
Pays: United Arab Emirates
ID NLM: 100960527

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 17 05 2019
revised: 12 12 2019
accepted: 12 12 2019
entrez: 14 7 2020
pubmed: 14 7 2020
medline: 14 7 2020
Statut: ppublish

Résumé

Nearly three decades ago, the association between Bladder cancer (BC) and DNA methylation has initially been reported. Indeed, in the recent years, the mechanism connecting these two has gained deeper insights. Still, the mediocre performance of DNA methylation markers in the clinics raises the major concern. Strikingly, whether it is the inter-individual methylation variations or the paucity of knowledge about methylation fingerprints lying within histologically distinct subtypes of BC requires critical discussion. In the future, besides identifying the initial causative factors, it will be important to illustrate the cascade of events that determines the fraction of the genome to convey altered methylation patterns specific towards each cancer type.

Identifiants

pubmed: 32655296
doi: 10.2174/1389202921666200102163422
pii: CG-21-34
pmc: PMC7324896
doi:

Types de publication

Journal Article

Langues

eng

Pagination

34-36

Informations de copyright

© 2020 Bentham Science Publishers.

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Auteurs

Amit Sharma (A)

1Department of Ophthalmology, University Clinic Bonn, Bonn, Germany; 2Department of Neurology, University Clinic Bonn, Bonn, Germany; 3Institute of Human Genetics, University Hospital of Bonn, Bonn, Germany; 4Department of Neonatology and Pediatric Intensive Care, Children's Hospital, University of Bonn, Bonn, Germany; 5Department of Urology, University Hospital Bonn, Bonn, Germany.

Heiko Reutter (H)

1Department of Ophthalmology, University Clinic Bonn, Bonn, Germany; 2Department of Neurology, University Clinic Bonn, Bonn, Germany; 3Institute of Human Genetics, University Hospital of Bonn, Bonn, Germany; 4Department of Neonatology and Pediatric Intensive Care, Children's Hospital, University of Bonn, Bonn, Germany; 5Department of Urology, University Hospital Bonn, Bonn, Germany.

Jörg Ellinger (J)

1Department of Ophthalmology, University Clinic Bonn, Bonn, Germany; 2Department of Neurology, University Clinic Bonn, Bonn, Germany; 3Institute of Human Genetics, University Hospital of Bonn, Bonn, Germany; 4Department of Neonatology and Pediatric Intensive Care, Children's Hospital, University of Bonn, Bonn, Germany; 5Department of Urology, University Hospital Bonn, Bonn, Germany.

Classifications MeSH