Ontology highlight
ABSTRACT: Significance
Glecirasib potently and selectively inhibits KRAS G12C and reduces ERK and AKT phosphorylation in KRAS G12C-mutant cancer cells, further inducing cell-cycle arrest and apoptosis. Glecirasib monotherapy leads to tumor regression in KRAS G12C-mutant animal models and shows synergistic effects with cetuximab or JAB-3312 (sitneprotafib).
SUBMITTER: Wang P
PROVIDER: S-EPMC12076188 | biostudies-literature | 2025 May
REPOSITORIES: biostudies-literature