Ontology highlight
ABSTRACT: Background
KRAS activating mutations are considered the most frequent oncogenic drivers and are correlated with radio-resistance in multiple cancers including non-small cell lung cancer (NSCLC) and colorectal cancer. Although KRAS was considered undruggable until recently, several KRAS inhibitors have recently reached clinical development. Among them, MRTX849 (Mirati Therapeutics) showed encouraging clinical outcomes for the treatment of selected patients with KRASG12C mutated NSCLC and colorectal cancers. In this work, we explore the ability of MRTX1257, a KRASG12C inhibitor analogous to MRTX849, to radio-sensitize KRASG12C+/+ mutated cell lines and tumors.Methods
Both in vitro and in vivo models of radiotherapy (RT) in association with MRT
SUBMITTER: Laurent PA
PROVIDER: S-EPMC10619254 | biostudies-literature | 2023 Oct
REPOSITORIES: biostudies-literature