Tuning protein synthesis for cancer therapy.
Ontology highlight
ABSTRACT: ~50% of colorectal cancers have an activating mutation in KRAS (encoding the KRAS proto-oncogene) and remain difficult to target in the clinic. We have recently shown that activation of KRAS protein alters the regulation of mRNA translation, increasing total protein synthesis, and maintaining elevated c-MYC (MYC proto-oncogene) expression. Targeting these pathways downstream of KRAS reveals a striking dependency that has potential for clinical translation.
SUBMITTER: Knight JRP
PROVIDER: S-EPMC8018481 | biostudies-literature |
REPOSITORIES: biostudies-literature
ACCESS DATA