MUC1 is a potential target to overcome trastuzumab resistance in breast cancer therapy.
Aysooda HosseinzadehParnaz MerikhianNazanin NaseriMohammad Reza EisavandLeila FarahmandPublished in: Cancer cell international (2022)
Although resistance is its major obstacle in cancer therapy, trastuzumab is the most successful agent in treating epidermal growth factor receptor 2 positive (HER2 +) breast cancer (BC). Some patients show resistance to trastuzumab, and scientists want to circumvent this problem. This review elaborately discusses possible resistance mechanisms to trastuzumab and introduces mucin 1 (MUC1) as a potential target efficient for overcoming such resistance. MUC1 belongs to the mucin family, playing the oncogenic/mitogenic roles in cancer cells and interacting with several other oncogenic receptors and pathways, such as HER2, β-catenin, NF-κB, and estrogen receptor (ERα). Besides, it has been established that MUC1- Cytoplasmic Domain (MUC1-CD) accelerates the development of resistance to trastuzumab and that silencing MUC1-C proto-oncogene is associated with increased sensitivity of HER2 + cells to trastuzumab-induced growth inhibitors. We mention why targeting MUC1 can be useful in overcoming trastuzumab resistance in cancer therapy.
Keyphrases
- epidermal growth factor receptor
- cancer therapy
- tyrosine kinase
- advanced non small cell lung cancer
- estrogen receptor
- metastatic breast cancer
- end stage renal disease
- drug delivery
- chronic kidney disease
- signaling pathway
- induced apoptosis
- ejection fraction
- peritoneal dialysis
- prognostic factors
- breast cancer cells