FGFR-TKI resistance in cancer: current status and perspectives.
Sitong YueYukun LiXiaojuan ChenJuan WangMeixiang LiYongheng ChenDaichao WuPublished in: Journal of hematology & oncology (2021)
Fibroblast growth factor receptors (FGFRs) play key roles in promoting the proliferation, differentiation, and migration of cancer cell. Inactivation of FGFRs by tyrosine kinase inhibitors (TKI) has achieved great success in tumor-targeted therapy. However, resistance to FGFR-TKI has become a concern. Here, we review the mechanisms of FGFR-TKI resistance in cancer, including gatekeeper mutations, alternative signaling pathway activation, lysosome-mediated TKI sequestration, and gene fusion. In addition, we summarize strategies to overcome resistance, including developing covalent inhibitors, developing dual-target inhibitors, adopting combination therapy, and targeting lysosomes, which will facilitate the transition to precision medicine and individualized treatment.
Keyphrases
- tyrosine kinase
- combination therapy
- chronic myeloid leukemia
- advanced non small cell lung cancer
- signaling pathway
- papillary thyroid
- current status
- epidermal growth factor receptor
- squamous cell
- epithelial mesenchymal transition
- genome wide
- gene expression
- oxidative stress
- cell proliferation
- cancer therapy
- fluorescent probe