Whole-Organ Genomic Characterization of Mucosal Field Effects Initiating Bladder Carcinogenesis.
DNA copy alterations
DNA methylation
Whole-organ map
bladder cancer
clonal expansion
clonal origins
field effect
founder mutation
gene signature
urothelial carcinoma
Journal
Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691
Informations de publication
Date de publication:
19 02 2019
19 02 2019
Historique:
received:
19
04
2018
revised:
12
12
2018
accepted:
25
01
2019
entrez:
21
2
2019
pubmed:
21
2
2019
medline:
11
4
2020
Statut:
ppublish
Résumé
We used whole-organ mapping to study the locoregional molecular changes in a human bladder containing multifocal cancer. Widespread DNA methylation changes were identified in the entire mucosa, representing the initial field effect. The field effect was associated with subclonal low-allele frequency mutations and a small number of DNA copy alterations. A founder mutation in the RNA splicing gene, ACIN1, was identified in normal mucosa and expanded clonally with an additional 21 mutations in progression to carcinoma. The patterns of mutations and copy number changes in carcinoma in situ and foci of carcinoma were almost identical, confirming their clonal origins. The pathways affected by the DNA copy alterations and mutations, including the Kras pathway, were preceded by the field changes in DNA methylation, suggesting that they reinforced mechanisms that had already been initiated by methylation. The results demonstrate that DNA methylation can serve as the initiator of bladder carcinogenesis.
Identifiants
pubmed: 30784602
pii: S2211-1247(19)30132-9
doi: 10.1016/j.celrep.2019.01.095
pii:
doi:
Substances chimiques
ACIN1 protein, human
0
Nuclear Proteins
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
2241-2256.e4Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved.