Treatment-Induced Tumor Dormancy through YAP-Mediated Transcriptional Reprogramming of the Apoptotic Pathway.
Adaptor Proteins, Signal Transducing
/ metabolism
Animals
Apoptosis
Cell Cycle Proteins
/ metabolism
Cell Line, Tumor
Cell Proliferation
Cell Survival
Cellular Senescence
Drug Resistance, Neoplasm
ErbB Receptors
/ metabolism
Female
Gene Deletion
Gene Expression Regulation, Neoplastic
Humans
Lung Neoplasms
/ metabolism
MAP Kinase Kinase 1
/ metabolism
Male
Mice
Mice, Knockout
Mutation
Signal Transduction
Transcription Factors
/ metabolism
Transcription, Genetic
YAP-Signaling Proteins
YAP
dormancy
drug resistance
drug tolerance
epidermal growth factor receptor
lung cancer
senescence
Journal
Cancer cell
ISSN: 1878-3686
Titre abrégé: Cancer Cell
Pays: United States
ID NLM: 101130617
Informations de publication
Date de publication:
13 01 2020
13 01 2020
Historique:
received:
17
05
2019
revised:
11
10
2019
accepted:
10
12
2019
entrez:
15
1
2020
pubmed:
15
1
2020
medline:
4
8
2020
Statut:
ppublish
Résumé
Eradicating tumor dormancy that develops following epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) treatment of EGFR-mutant non-small cell lung cancer, is an attractive therapeutic strategy but the mechanisms governing this process are poorly understood. Blockade of ERK1/2 reactivation following EGFR TKI treatment by combined EGFR/MEK inhibition uncovers cells that survive by entering a senescence-like dormant state characterized by high YAP/TEAD activity. YAP/TEAD engage the epithelial-to-mesenchymal transition transcription factor SLUG to directly repress pro-apoptotic BMF, limiting drug-induced apoptosis. Pharmacological co-inhibition of YAP and TEAD, or genetic deletion of YAP1, all deplete dormant cells by enhancing EGFR/MEK inhibition-induced apoptosis. Enhancing the initial efficacy of targeted therapies could ultimately lead to prolonged treatment responses in cancer patients.
Identifiants
pubmed: 31935369
pii: S1535-6108(19)30576-8
doi: 10.1016/j.ccell.2019.12.006
pmc: PMC7146079
mid: NIHMS1569353
pii:
doi:
Substances chimiques
Adaptor Proteins, Signal Transducing
0
Cell Cycle Proteins
0
Transcription Factors
0
YAP-Signaling Proteins
0
YAP1 protein, human
0
Yap1 protein, mouse
0
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
MAP Kinase Kinase 1
EC 2.7.12.2
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
104-122.e12Subventions
Organisme : NCI NIH HHS
ID : P30 CA016087
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL105373
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA154303
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA222218
Pays : United States
Organisme : NCI NIH HHS
ID : R35 CA220497
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA233800
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA135257
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA006516
Pays : United States
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2019 Elsevier Inc. All rights reserved.
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