CDK4/6 inhibitor palbociclib targets β-catenin in KRAS-mutant tumors Skip to content The CRC Digest CDK4/6 inhibitor palbociclib targets β-catenin in KRAS-mutant tumors Preclinical research identified palbociclib as an unexpected suppressor of β-catenin signaling that synergizes with KRAS or ERK5 inhibition in colorectal cancer models. (Journal of Translational Medicine) This content is informational only and does not constitute
CRC Research Finding Skip to content The CRC Digest ◇ KRAS-mutant colorectal cancers show variable response to RAS inhibitors Preclinical research found that KRAS-mutant colorectal cancer models respond differently to RAS(ON) inhibitor RMC-7977 based on PI3K signaling and cyclin D1 expression patterns, with combined RAS and PI3K inhibition showing synergistic effects in some
KRAS G13D-mutant metastatic rectal cancer achieves 16.6 months disease control with TAS-102 plus bevacizumab Skip to content The CRC Digest KRAS G13D-mutant metastatic rectal cancer achieves 16.6 months disease control with TAS-102 plus bevacizumab A 57-year-old man with KRAS G13D-mutant metastatic rectal cancer and fluoropyrimidine intolerance achieved approximately 16.6 months of disease control with trifluridine/tipiracil plus bevacizumab integrated with liver-directed treatments,
Novel SOS1 Inhibitors Show Potent Activity Against KRAS-Driven CRC Skip to content The CRC Digest Novel SOS1 Inhibitors Show Potent Activity Against KRAS-Driven CRC Highly potent and selective SOS1 inhibitors disrupted the SOS1-KRAS interaction, inhibited nucleotide exchange in wild-type and multiple KRAS variants, and showed submicromolar anti-proliferative activity in colorectal cancer cells. (J Med Chem) This content is informational