Dark and bright side of targeting fibroblast growth factor receptor 4 in the liver

被引:23
作者
Gadaleta, Raffaella Maria [1 ]
Moschetta, Antonio [1 ]
机构
[1] Univ Bari, Dept Interdisciplinary Med, Giulio Cesare 11, I-70100 Bari, Italy
关键词
Fibroblast Growth Factor Receptor 4; Fibroblast Growth Factor 19; Hepatocellular Carcinoma; Liver Fibrosis; Non-Alcoholic Steatohepatitis; BILE-ACID SYNTHESIS; FARNESOID-X-RECEPTOR; HEPATOCELLULAR-CARCINOMA CELLS; NONALCOHOLIC STEATOHEPATITIS; SERUM CONCENTRATIONS; SELECTIVE INHIBITOR; FIBROSIS STAGE; METABOLIC-RATE; DOUBLE-BLIND; COPY NUMBER;
D O I
10.1016/j.jhep.2021.07.029
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Fibroblast growth factor (FGF) receptor 4 (FGFR4) and its cognate ligand, FGF19, are implicated in a rangeof cellular processes, including differentiation, metabolism and proliferation. Indeed, their aberrantactivation has been associated with the development of hepatic tumours. Despite great advances in earlydiagnosis and the development of new therapies, liver cancer is still associated with a high mortality rate,owing primarily to high molecular heterogeneity and unclear molecular targeting. The development ofFGFR4 inhibitors is a promising tool in patients with concomitant supraphysiological levels of FGF19 andseveral clinical trials are testing these treatments for patients with advanced hepatocellular carcinoma(HCC). Conversely, using FGF19 analogues to activate FGFR4-KLOTHObrepresents a novel therapeuticstrategy in patients presenting with cholestatic liver disorders and non-alcoholic steatohepatitis, whichcould potentially prevent the development of metabolic HCC. Herein, we provide an overview of thecurrently available therapeutic options for targeting FGFR4 in HCC and other liver diseases, highlightingthe need to carefully stratify patients and personalise therapeutic strategies. (c) 2021 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1440 / 1451
页数:12
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