DNA damage signalling as an anti-cancer barrier in gastric intestinal metaplasia.
Biopsy
/ methods
DNA Damage
/ genetics
DNA Methylation
Female
Gastric Mucosa
/ pathology
Gene Expression Regulation, Neoplastic
Histones
/ genetics
Humans
Hyaluronan Receptors
/ analysis
Male
Metaplasia
/ genetics
Middle Aged
Minichromosome Maintenance Complex Component 2
/ genetics
MutL Protein Homolog 1
/ genetics
Mutation
Protective Factors
Rad52 DNA Repair and Recombination Protein
/ genetics
Signal Transduction
Stomach Neoplasms
/ genetics
Werner Syndrome Helicase
/ genetics
DNA damage
gastric cancer
gastric metaplasia
Journal
Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
received:
11
05
2019
revised:
20
12
2019
accepted:
21
12
2019
pubmed:
16
1
2020
medline:
10
4
2021
entrez:
16
1
2020
Statut:
ppublish
Résumé
Intestinal metaplasia (IM) is a premalignant stage that poses a greater risk for subsequent gastric cancer (GC). However, factors regulating IM to GC progression remain unclear. Previously, activated DNA damage response (DDR) signalling factors were shown to engage tumour-suppressive networks in premalignant lesions. Here, we interrogate the relationship of DDR signalling to mutational accumulation in IM lesions. IM biopsies were procured from the gastric cancer epidemiology programme, an endoscopic surveillance programme where biopsies have been subjected to (epi)genomic characterisation. IM samples were classified as genome-stable or genome-unstable based on their mutational burden/somatic copy-number alteration (CNA) profiles. Samples were probed for DDR signalling and cell proliferation, using the markers γH2AX and MCM2, respectively. The expression of the gastric stem cell marker, CD44v9, was also assessed. Tissue microarrays representing the GC progression spectrum were included. MCM2-positivity increased during GC progression, while γH2AX-positivity showed modest increase from normal to gastritis and IM stages, with further increase in GC. γH2AX levels correlated with the extent of chronic inflammation. Interestingly, genome-stable IM lesions had higher γH2AX levels underscoring a protective anti-cancer role for DDR signalling. In contrast, genome-unstable IM lesions with higher mutational burden/CNAs had lower γH2AX levels, elevated CD44v9 expression and modest promoter hypermethylation of DNA repair genes Our data suggest that IM lesions with active DDR will likely experience a longer latency at the premalignant state until additional hits that override DDR signalling clonally expand and promote progression. These observations provide insights on the factors governing IM progression.
Identifiants
pubmed: 31937549
pii: gutjnl-2019-319002
doi: 10.1136/gutjnl-2019-319002
pmc: PMC7497583
doi:
Substances chimiques
CD44v9 antigen
0
H2AX protein, human
0
Histones
0
Hyaluronan Receptors
0
MLH1 protein, human
0
RAD52 protein, human
0
Rad52 DNA Repair and Recombination Protein
0
MutL Protein Homolog 1
EC 3.6.1.3
MCM2 protein, human
EC 3.6.4.12
Minichromosome Maintenance Complex Component 2
EC 3.6.4.12
WRN protein, human
EC 3.6.4.12
Werner Syndrome Helicase
EC 3.6.4.12
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1738-1749Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.
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