MET Oncogene Targeting for Cancer Immunotherapy.
MET antibody
MET oncogene
MET tyrosine kinase inhibitors
cellular immunotherapy
immunotherapy
targeted therapy
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
01 Jun 2024
01 Jun 2024
Historique:
received:
30
04
2024
revised:
29
05
2024
accepted:
30
05
2024
medline:
19
6
2024
pubmed:
19
6
2024
entrez:
19
6
2024
Statut:
epublish
Résumé
The MET receptor is one of the main drivers of 'invasive growth', a multifaceted biological response essential during embryonic development and tissue repair that is usurped by cancer cells to induce and sustain the malignant phenotype. MET stands out as one of the most important oncogenes activated in cancer and its inhibition has been explored since the initial era of cancer-targeted therapy. Different approaches have been developed to hamper MET signaling and/or reduce MET (over)expression as a hallmark of transformation. Considering the great interest gained by cancer immunotherapy, this review evaluates the opportunity of targeting MET within therapeutic approaches based on the exploitation of immune functions, either in those cases where MET impairment is crucial to induce an effective response (i.e., when MET is the driver of the malignancy), or when blocking MET represents a way for potentiating the treatment (i.e., when MET is an adjuvant of tumor fitness).
Identifiants
pubmed: 38892318
pii: ijms25116109
doi: 10.3390/ijms25116109
pii:
doi:
Substances chimiques
Proto-Oncogene Proteins c-met
EC 2.7.10.1
MET protein, human
EC 2.7.10.1
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : University of Torino
ID : RiLo 2022
Organisme : Associazione Italiana Ricerca sul Cancro (AIRC)
ID : grant 5 per Mille 2018 - ID 21052
Organisme : Associazione Italiana Ricerca sul Cancro (AIRC)
ID : grant IG-2017 - ID 20259