| Literature DB >> 33568192 |
Sitong Yue1, Yukun Li2, Xiaojuan Chen1, Juan Wang2, Meixiang Li2, Yongheng Chen3,4, Daichao Wu5,6,7,8.
Abstract
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.Entities:
Keywords: Drug resistance; FGFR; Gatekeeper mutation; Lysosome sequestration; Tyrosine kinase inhibitor
Year: 2021 PMID: 33568192 PMCID: PMC7876795 DOI: 10.1186/s13045-021-01040-2
Source DB: PubMed Journal: J Hematol Oncol ISSN: 1756-8722 Impact factor: 17.388