Assessment of KRAS
KRAS G12C inhibitors
KRAS mutation G12C
clinical trials
colorectal cancer
resistance
Journal
Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867
Informations de publication
Date de publication:
2024
2024
Historique:
received:
04
04
2024
accepted:
06
06
2024
medline:
9
7
2024
pubmed:
9
7
2024
entrez:
9
7
2024
Statut:
epublish
Résumé
Colorectal cancer (CRC) is a highly prevalent and lethal cancer worldwide. Approximately 45% of CRC patients harbor a gain-in-function mutation in KRAS. KRAS is the most frequently mutated oncogene accounting for approximately 25% of all human cancers. Gene mutations in KRAS cause constitutive activation of the KRAS protein and MAPK/AKT signaling, resulting in unregulated proliferation and survival of cancer cells and other aspects of malignant transformation, progression, and metastasis. While KRAS has long been considered undruggable, the FDA recently approved two direct acting KRAS inhibitors, Sotorasib and Adagrasib, that covalently bind and inactivate KRAS
Identifiants
pubmed: 38978742
doi: 10.3389/fonc.2024.1412435
pmc: PMC11228624
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
1412435Informations de copyright
Copyright © 2024 Piazza, Chandrasekaran, Maxuitenko and Budhwani.
Déclaration de conflit d'intérêts
Author GP is a co-founder of ADT Pharmaceuticals Inc. and consultant. Author KIB is a co-founder and CEO-Scientist of CerFlux. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.