FGF Family: From Drug Development to Clinical Application

被引:134
作者
Hui, Qi [1 ]
Jin, Zi [1 ]
Li, Xiaokun [1 ,2 ]
Liu, Changxiao [1 ,3 ]
Wang, Xiaojie [1 ,2 ]
机构
[1] Wenzhou Med Univ, Sch Pharm, Chashan Univ Pk, Wenzhou 325035, Peoples R China
[2] Wenzhou Med Univ, Key Lab Biotechnol Pharmaceut Engn, Chashan Univ Pk, Wenzhou 325035, Peoples R China
[3] Tianjin Inst Pharmaceut Res, State Key Lab Drug Delivery Technol & Pharmacokin, 308 Anshan West Rd, Tianjin 300193, Peoples R China
基金
中国国家自然科学基金;
关键词
fibroblast growth factor; wound healing; metabolic regulation; fibroblast growth factor receptor inhibitor; drug development; clinical application; FIBROBLAST-GROWTH-FACTOR; X-LINKED HYPOPHOSPHATEMIA; ANTI-FGF23 ANTIBODY KRN23; FACTOR RECEPTORS FGFRS; CHRONIC KIDNEY-DISEASE; BREAST-CANCER; GENE AMPLIFICATION; RANDOMIZED-TRIAL; GASTRIC-CANCER; CARDIOVASCULAR-DISEASE;
D O I
10.3390/ijms19071875
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fibroblast growth factor (FGF) belongs to a large family of growth factors. FGFs use paracrine or endocrine signaling to mediate a myriad of biological and pathophysiological process, including angiogenesis, wound healing, embryonic development, and metabolism regulation. FGF drugs for the treatment of burn and ulcer wounds are now available. The recent discovery of the crucial roles of the endocrine-acting FGF19 subfamily in maintaining homeostasis of bile acid, glucose, and phosphate further extended the activity profile of this family. Here, the applications of recombinant FGFs for the treatment of wounds, diabetes, hypophosphatemia, the development of FGF receptor inhibitors as anti-neoplastic drugs, and the achievements of basic research and applications of FGFs in China are reviewed.
引用
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页数:15
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