Therapeutic potential of the endocrine fibroblast growth factors FGF19, FGF21 and FGF23

被引:419
作者
Degirolamo, Chiara [1 ,2 ]
Sabba, Carlo [1 ]
Moschetta, Antonio [1 ,2 ]
机构
[1] Univ Bari Aldo Moro, Clin Med Cesare Frugoni, Dipartimento Interdisciplinare Med, I-70124 Bari, Italy
[2] IRCCS, Ist Tumori Giovanni Paolo 2, I-70124 Bari, Italy
关键词
BILE-ACID SYNTHESIS; FARNESOID-X-RECEPTOR; INCREASES ENERGY-EXPENDITURE; LEFT-VENTRICULAR HYPERTROPHY; ORPHAN NUCLEAR RECEPTOR; PPAR-ALPHA ACTIVATION; FACTOR; 21; EXPRESSION; INDUCED OBESE MICE; VITAMIN-D; BETA-KLOTHO;
D O I
10.1038/nrd.2015.9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
The endocrine fibroblast growth factors (FGFs), FGF19, FGF21 and FGF23, are critical for maintaining whole-body homeostasis, with roles in bile acid, glucose and lipid metabolism, modulation of vitamin D and phosphate homeostasis and metabolic adaptation during fasting. Given these functions, the endocrine FGFs have therapeutic potential in a wide array of chronic human diseases, including obesity, type 2 diabetes, cancer, and kidney and cardiovascular disease. However, the safety and feasibility of chronic endocrine FGF administration has been challenged, and FGF analogues and mimetics are now being investigated. Here, we discuss current knowledge of the complex biology of the endocrine FGFs and assess how this may be harnessed therapeutically.
引用
收藏
页码:51 / 69
页数:19
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