ARID1A mutations in lung cancer: biology, prognostic role, and therapeutic implications.
ARID1A
SWI/SNF complex
cell cycle regulation
epithelial–mesenchymal transition
lung cancer
metabolic reprogramming
Journal
Trends in molecular medicine
ISSN: 1471-499X
Titre abrégé: Trends Mol Med
Pays: England
ID NLM: 100966035
Informations de publication
Date de publication:
Aug 2023
Aug 2023
Historique:
received:
06
04
2023
revised:
20
04
2023
accepted:
21
04
2023
medline:
17
7
2023
pubmed:
14
5
2023
entrez:
13
5
2023
Statut:
ppublish
Résumé
Mutations in the AT-interacting domain-rich protein 1A (ARID1A) gene, a critical component of the switch/sucrose nonfermentable (SWI/SNF) complex, are frequently found in most human cancers. Approximately 5-10% of lung cancers carry ARID1A mutations. ARID1A loss in lung cancer correlates with clinicopathological features and poor prognosis. Co-mutation of ARID1A and epidermal growth factor receptor (EGFR) results in the limited efficacy of EGFR tyrosine kinase inhibitors (EGFR-TKIs) but increases the clinical benefit of immune checkpoint inhibitors (ICIs). ARID1A gene mutation plays a role in cell cycle regulation, metabolic reprogramming, and epithelial-mesenchymal transition. We present the first comprehensive review of the relationship between ARID1A gene mutations and lung cancer and discuss the potential of ARID1A as a new molecular target.
Identifiants
pubmed: 37179132
pii: S1471-4914(23)00075-8
doi: 10.1016/j.molmed.2023.04.005
pii:
doi:
Substances chimiques
DNA-Binding Proteins
0
Transcription Factors
0
Nuclear Proteins
0
ErbB Receptors
EC 2.7.10.1
ARID1A protein, human
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
646-658Informations de copyright
Copyright © 2023 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests S.L. has received research support from BerGenBio, Bristol Myers Squibb, Eli Lilly and Company, Roche, and ADC Therapeutics. S.L. has received speaker honoraria from BerGenBio, Bristol Myers Squibb, Boehringer Ingelheim, Eli Lilly and Company, Roche, Medac, Sanofi Aventis, Novartis, AstraZeneca, Pfizer, Takeda Pharmaceutical Company, Amgen, Bayer, Janssen Pharmaceuticals, and Merck. S.L. is consultant to BerGenBio, Bristol Myers Squibb, Boehringer Ingelheim, Eli Lilly and Company, Roche, Medac, Sanofi Aventis, Novartis, AstraZeneca, Pfizer, Takeda Pharmaceutical Company, Amgen, Bayer, Janssen Pharmaceuticals, and Merck. S.L. has received travel support from BerGenBio, Bristol Myers Squibb, Boehringer Ingelheim, Eli Lilly and Company, Roche, Medac, Sanofi Aventis, Novartis, AstraZeneca, Pfizer, Takeda Pharmaceutical Company, Amgen, Bayer, Janssen Pharmaceuticals, and Merck. Author S.L. has received drugs for research from Bristol Myers Squibb. All other authors have no financial or any other competing interests.