Fibroblast Growth Factor Receptor 4 Targeting in Cancer: New Insights into Mechanisms and Therapeutic Strategies

被引:67
|
作者
Lang, Liwei [1 ]
Teng, Yong [1 ,2 ,3 ]
机构
[1] Augusta Univ, Dent Coll Georgia, Dept Oral Biol & Diagnost Sci, Augusta, GA 30912 USA
[2] Augusta Univ, Med Coll Georgia, Dept Biochem & Mol Biol, Georgia Canc Ctr, Augusta, GA 30912 USA
[3] Augusta Univ, Coll Allied Hlth, Dept Med Lab Imaging & Radiol Sci, Augusta, GA 30912 USA
关键词
FGFR4; FGF19; gene regulation; cancer signaling; anticancer; HEPATOCELLULAR-CARCINOMA CELLS; MESENCHYMAL TRANSITION; SELECTIVE INHIBITOR; MEMBRANE-PROTEINS; 11Q13; AMPLICON; LIVER-CANCER; FGFR4; FGF19; RESISTANCE; IDENTIFICATION;
D O I
10.3390/cells8010031
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fibroblast growth factor receptor 4 (FGFR4), a tyrosine kinase receptor for FGFs, is involved in diverse cellular processes, including the regulation of cell proliferation, differentiation, migration, metabolism, and bile acid biosynthesis. High activation of FGFR4 is strongly associated with the amplification of its specific ligand FGF19 in many types of solid tumors and hematologic malignancies, where it acts as an oncogene driving the cancer development and progression. Currently, the development and therapeutic evaluation of FGFR4-specific inhibitors, such as BLU9931 and H3B-6527, in animal models and cancer patients, are paving the way to suppress hyperactive FGFR4 signaling in cancer. This comprehensive review not only covers the recent discoveries in understanding FGFR4 regulation and function in cancer, but also reveals the therapeutic implications and applications regarding emerging anti-FGFR4 agents. Our aim is to pinpoint the potential of FGFR4 as a therapeutic target and identify new avenues for advancing future research in the field.
引用
收藏
页数:13
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