Expression of neurofibromin 1 in colorectal cancer and cetuximab resistance. [PDF]
Neurofibromin 1 (NF1) is a tumor suppressor that has been previously reported to regulate RAS-MAPK signaling. The present study investigated the possible relationship between NF1 expression and anti-EGFR antibody (cetuximab) sensitivity in colorectal ...
Tak E +11 more
europepmc +5 more sources
Inhibition of autocrine HGF maturation overcomes cetuximab resistance in colorectal cancer. [PDF]
Although amplifications and mutations in receptor tyrosine kinases (RTKs) act as bona fide oncogenes, in most cancers, RTKs maintain moderate expression and remain wild-type.
Jones VT +17 more
europepmc +5 more sources
Negative correlation between acetyl-CoA acyltransferase 2 and cetuximab resistance in colorectal cancer [PDF]
The emergence of anti-EGFR therapy has revolutionized the treatment of colorectal cancer (CRC). However, not all patients respond consistently well.
Yuan Yitao +13 more
doaj +3 more sources
PRSS contributes to cetuximab resistance in colorectal cancer. [PDF]
PRSS leads to cetuximab resistance by cleaving the drug, and SPINK1 or modified mAbs can avoid PRSS cleavage. Cetuximab improves the survival of patients with metastatic colorectal cancer.
Tan Z +20 more
europepmc +5 more sources
MiR-135b-5p promotes cetuximab resistance in colorectal cancer by regulating FOXN3. [PDF]
Despite advances in targeted therapies, primary and acquired resistance make the treatment of colorectal cancer (CRC) a pressing issue to be resolved. According to reports, the development of CRC is linked to miRNA dysregulation.
Peng C +5 more
europepmc +5 more sources
BET Inhibition Overcomes Receptor Tyrosine Kinase-Mediated Cetuximab Resistance in HNSCC. [PDF]
Cetuximab, the FDA-approved anti-EGFR antibody for head and neck squamous cell carcinoma (HNSCC), has displayed limited efficacy due to the emergence of intrinsic and acquired resistance. We and others have demonstrated that cetuximab resistance in HNSCC
Leonard B +8 more
europepmc +7 more sources
3-Bromopyruvate overcomes cetuximab resistance in human colorectal cancer cells by inducing autophagy-dependent ferroptosis. [PDF]
Colorectal cancer (CRC) remains a leading cause of cancer-related death worldwide. Cetuximab, in combination with chemotherapy, is effective for treating patients with wild-type KRAS/BRAF metastatic CRC (mCRC).
Mu M +6 more
europepmc +2 more sources
IGF2BP3 promotes the progression of colorectal cancer and mediates cetuximab resistance by stabilizing EGFR mRNA in an m6A-dependent manner. [PDF]
Insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3), an RNA-binding protein, is associated with tumorigenesis and progression. However, the exact molecular mechanisms of IGF2BP3 in colorectal cancer (CRC) oncogenesis, progression, and drug ...
Chen LJ +14 more
europepmc +2 more sources
Epacadostat Overcomes Cetuximab Resistance in Colorectal Cancer by Targeting IDO-Mediated Tryptophan Metabolism. [PDF]
Primary or acquired mutations in RAS/RAF genes resulting in cetuximab resistance have limited its clinical application in colorectal cancer (CRC) patients. The mechanism of this resistance remains unclear.
Zhou Y +5 more
europepmc +2 more sources
Exosomes derived from MDR cells induce cetuximab resistance in CRC via PI3K/AKT signaling‑mediated Sox2 and PD‑L1 expression. [PDF]
The anti-EGFR antibody cetuximab is used as a first-line targeted therapeutic drug in colorectal cancer. It has previously been reported that the efficacy of the EGFR antibody cetuximab is limited by the emergence of acquired drug resistance.
Wei Z +9 more
europepmc +2 more sources

