PIK3C3 inhibition enhances 5-FU sensitivity in KRAS-mutant cells, opposite effect in KRAS-wild-type Skip to content The CRC Digest ◇ RESEARCH PIK3C3 inhibition enhances 5-FU sensitivity in KRAS-mutant cells, opposite effect in KRAS-wild-type Laboratory study found PIK3C3 knockdown increased 5-fluorouracil resistance in KRAS-wild-type cells but enhanced sensitivity in KRAS-mutant cells, potentially through thymidylate synthase regulation. (Cancer Medicine) This content is informational only and does
Pharmacokinetic method developed for pan-RAS inhibitor Skip to content The CRC Digest ▸ TREATMENT Pharmacokinetic method developed for pan-RAS inhibitor Researchers validated a mass spectrometry assay to measure daraxonrasib, an oral pan-RAS inhibitor in clinical evaluation for colorectal cancer, in canine plasma and whole blood, supporting pharmacokinetic characterization of the investigational drug. (Biomed Chromatogr) This content is
Molecular profiling study identifies clinicopathological factors linked to dMMR/MSI-H status Skip to content The CRC Digest Molecular profiling study identifies clinicopathological factors linked to dMMR/MSI-H status In 272 resected colorectal cancers, dMMR/MSI-H was present in 9.6% of tumors and independently associated with younger age, proximal tumor location, and poor differentiation. (Clinical Therapeutics) This content is informational only
Large cohort study maps RAS-pathway mutation patterns in 1,243 colorectal cancer samples Skip to content The CRC Digest ◇ RESEARCH Large cohort study maps RAS-pathway mutation patterns in 1,243 colorectal cancer samples Whole-exome sequencing revealed KRAS mutations in 35.3% of tumors, BRAF V600E in 6.8%, and PIK3CA in 17.8%, with KRAS-PIK3CA co-mutations occurring in 10.1% overall; RAS-mutant tumors
KRAS, NRAS, and BRAF mutation frequencies reported in Iranian metastatic CRC cohort Skip to content The CRC Digest KRAS, NRAS, and BRAF mutation frequencies reported in Iranian metastatic CRC cohort Among 83 patients with metastatic colorectal cancer, mutation frequencies were 47% for KRAS, 14.5% for NRAS, and 6% for BRAF; BRAF mutations were significantly more frequent in patients under 50 years