FGFR-TKI resistance in cancer: current status and perspectives

被引:0
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作者
Sitong Yue
Yukun Li
Xiaojuan Chen
Juan Wang
Meixiang Li
Yongheng Chen
Daichao Wu
机构
[1] Central South University,Department of Oncology, Laboratory of Structural Biology, NHC Key Laboratory of Cancer Proteomics, State Local Joint Engineering Laboratory for Anticancer Drugs, Xiangya Hospital
[2] University of South China,Clinical Anatomy and Reproductive Medicine Application Institute, Department of Histology and Embryology, Hunan Province Key Laboratory of Cancer Cellular and Molecular Pathology
[3] Central South University,National Clinical Research Center for Geriatric Disorders, Xiangya Hospital
[4] University of Maryland Institute for Bioscience and Biotechnology Research,W.M. Keck Laboratory for Structural Biology
来源
Journal of Hematology & Oncology | / 14卷
关键词
FGFR; Tyrosine kinase inhibitor; Drug resistance; Gatekeeper mutation; Lysosome sequestration;
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摘要
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.
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