Fibroblast growth factors 19 and 21 in acute liver damage

被引:13
作者
Shan, Zhao [1 ]
Alvarez-Sola, Gloria [2 ,3 ]
Uriarte, Iker [2 ,3 ]
Arechederra, Maria [2 ,3 ]
Fernandez-Barrena, Maite G. [2 ,3 ]
Berasain, Carmen [2 ,3 ,4 ]
Ju, Cynthia [1 ]
Avila, Matias A. [2 ,3 ,4 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Dept Anesthesiol, McGovern Med Sch, Houston, TX 77030 USA
[2] Univ Navarra, Hepatol Program, Ctr Appl Med Res CIMA, Pamplona, Spain
[3] Carlos III Inst Hlth, CIBERehd, Pamplona, Spain
[4] Inst Invest Sanitarias Navarra IDISNA, Pamplona, Spain
基金
美国国家卫生研究院;
关键词
Acute liver injury; fibroblast growth factor 19 (FGF19); fibroblast growth factor 21 (FGF21); ACETAMINOPHEN-INDUCED HEPATOTOXICITY; FULMINANT HEPATIC-FAILURE; BILE-ACID SYNTHESIS; FATTY LIVER; SKELETAL-MUSCLE; METABOLIC-RATE; BETA-KLOTHO; FGF21; FGF19; REGENERATION;
D O I
10.21037/atm.2018.05.26
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Currently there are very few pharmacological options available to treat acute liver injury. Because its natural exposure to noxious stimuli the liver has developed a strong endogenous hepatoprotective capacity. Indeed, experimental evidence exposed a variety of endogenous hepatic and systemic responses naturally activated to protect the hepatic parenchyma and to foster liver regeneration, therefore preserving individual's survival. The fibroblast growth factor (FGF) family encompasses a range of polypeptides with important effects on cellular differentiation, growth survival and metabolic regulation in adult organisms. Among these FGFs, FGF19 and FGF21 are endocrine hormones that profoundly influence systemic metabolism but also exert important hepatoprotective activities. In this review, we revisit the biology of these factors and highlight their potential application for the clinical management of acute liver injury.
引用
收藏
页数:11
相关论文
共 113 条
[1]  
Abu-Amara M, 2009, COCHRANE DB SYST REV, V248
[2]   The breadth of FGF21's metabolic actions are governed by FGFR1 in adipose tissue [J].
Adams, Andrew C. ;
Yang, Chaofeng ;
Coskun, Tamer ;
Cheng, Christine C. ;
Gimeno, Ruth E. ;
Luo, Yongde ;
Kharitonenkov, Alexei .
MOLECULAR METABOLISM, 2013, 2 (01) :31-37
[3]   Engineered fibroblast growth factor 19 protects from acetaminophen-induced liver injury and stimulates aged liver regeneration in mice [J].
Alvarez-Sola, Gloria ;
Uriarte, Iker ;
Latasa, Maria U. ;
Jimenez, Maddalen ;
Barcena-Varela, Marina ;
Santamaria, Eva ;
Urtasun, Raquel ;
Rodriguez-Ortigosa, Carlos ;
Prieto, Jesus ;
Corrales, Fernando J. ;
Baulies, Anna ;
Garcia-Ruiz, Carmen ;
Fernandez-Checa, Jose C. ;
Berraondo, Pedro ;
Fernandez-Barrena, Maite G. ;
Berasain, Carmen ;
Avila, Matias A. .
CELL DEATH & DISEASE, 2017, 8 :e3083-e3083
[4]   Fibroblast growth factor 15/19 (FGF15/19) protects from diet-induced hepatic steatosis: development of an FGF19-based chimeric molecule to promote fatty liver regeneration [J].
Alvarez-Sola, Gloria ;
Uriarte, Iker ;
Ujue Latasa, M. ;
Fernandez-Barrena, Maite G. ;
Urtasun, Raquel ;
Elizalde, Maria ;
Barcena-Varela, Marina ;
Jimenez, Maddalen ;
Chang, Haisul C. ;
Barbero, Roberto ;
Catalan, Victoria ;
Rodriguez, Amaia ;
Fruhbeck, Gema ;
Gallego-Escuredo, Jose M. ;
Gavalda-Navarr, Aleix ;
Villarroya, Francesc ;
Rodriguez-Ortigosa, Carlos M. ;
Corrales, Fernando J. ;
Prieto, Jesus ;
Berraondo, Pedro ;
Berasain, Carmen ;
Avila, Matias A. .
GUT, 2017, 66 (10) :1818-1828
[5]   Fibroblast Growth Factor 15/19 in Hepatocarcinogenesis [J].
Alvarez-Sola, Gloria ;
Uriarte, Iker ;
Ujue Latasa, M. ;
Urtasun, Raquel ;
Barcena-Varela, Marina ;
Elizalde, Maria ;
Jimenez, Maddalen ;
Rodriguez-Ortigosa, Carlos M. ;
Corrales, Fernando J. ;
Fernandez-Barrena, Maite G. ;
Berasain, Carmen ;
Avila, Matias A. .
DIGESTIVE DISEASES, 2017, 35 (03) :158-165
[6]   Drug-induced liver disease in 2006 [J].
Arundel, Cherinne ;
Lewis, James H. .
CURRENT OPINION IN GASTROENTEROLOGY, 2007, 23 (03) :244-254
[7]   Fulminant hepatic failure secondary to acetaminophen poisoning: A systematic review and meta-analysis of prognostic criteria determining the need for liver transplantation [J].
Bailey, B ;
Amre, DK ;
Gaudreault, P .
CRITICAL CARE MEDICINE, 2003, 31 (01) :299-305
[8]   The FGF family: biology, pathophysiology and therapy [J].
Beenken, Andrew ;
Mohammadi, Moosa .
NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (03) :235-253
[9]   Fibroblast growth factor 19 regulates skeletal muscle mass and ameliorates muscle wasting in mice [J].
Benoit, Berengere ;
Meugnier, Emmanuelle ;
Castelli, Martina ;
Chanon, Stephanie ;
Vieille-Marchiset, Aurelie ;
Durand, Christine ;
Bendridi, Nadia ;
Pesenti, Sandra ;
Monternier, Pierre-Axel ;
Durieux, Anne-Cecile ;
Freyssenet, Damien ;
Rieusset, Jennifer ;
Lefai, Etienne ;
Vidal, Hubert ;
Ruzzin, Jerome .
NATURE MEDICINE, 2017, 23 (08) :990-+
[10]   Acute-on-chronic liver failure [J].
Bernal, William ;
Jalan, Rajiv ;
Quaglia, Alberto ;
Simpson, Kenneth ;
Wendon, Julia ;
Burroughs, Andrew .
LANCET, 2015, 386 (10003) :1576-1587