PNPLA3-A Potential Therapeutic Target for Personalized Treatment of Chronic Liver Disease

被引:55
作者
Dong, Xiaocheng Charlie [1 ]
机构
[1] Indiana Univ Sch Med, Dept Biochem & Mol Biol, Ctr Diabet & Metab Dis, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
PNPLA3; rs738409; nonalcoholic steatohepatitis; alcoholic liver disease; fibrosis; cirrhosis; hepatocellular carcinoma; NONALCOHOLIC FATTY LIVER; SUPERFAMILY MEMBER 2; GREATER-THAN-G; GLUCOKINASE REGULATORY PROTEIN; GENOME-WIDE ASSOCIATION; 3 GENE PNPLA3; TRIGLYCERIDE HYDROLASE ACTIVITY; HEPATOCELLULAR-CARCINOMA; I148M VARIANT; TM6SF2; RS58542926;
D O I
10.3389/fmed.2019.00304
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patatin-like phospholipase domain-containing protein 3 (PNPLA3) is a lipid droplet-associated protein that has been shown to have hydrolase activity toward triglycerides and retinyl esters. The first evidence of PNPLA3 being associated with fatty liver disease was revealed by a genome-wide association study (GWAS) of Hispanic, African American, and European American individuals in the Dallas Heart Study back in 2008. Since then, numerous GWAS reports have shown that PNPLA3 rs738409[G] (148M) variant is associated with hepatic triglyceride accumulation (steatosis), inflammation, fibrosis, cirrhosis, and even hepatocellular carcinoma regardless of etiologies including alcohol- or obesity-related and others. The frequency of PNPLA3(148M) variant ranges from 17% in African Americans, 23% in European Americans, to 49% in Hispanics in the Dallas Heart Study. Due to high prevalence of obesity and alcohol consumption in modern societies, the PNPLA3(148M) gene variant and environment interaction poses a serious concern for public health, especially chronic liver diseases including alcohol-related liver disease (ALD) and nonalcoholic fatty liver disease (NAFLD). Therefore, PNPLA3(148M) variant is a potential therapeutic target for chronic liver disease in the rs738409 allele carriers. Currently, there is no approved drug specifically targeting the PNPLA3(148M) variant yet. With additional mechanistic studies, novel therapeutic strategies are expected to be developed for the treatment of the PNPLA3(148M) variant-associated chronic liver diseases in the near future.
引用
收藏
页数:11
相关论文
共 171 条
[1]   HCV-Associated Liver Fibrosis and HSD17B13 [J].
About, Fredegonde ;
Abel, Laurent ;
Cobat, Aurelie .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 379 (19) :1875-1876
[2]   A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease [J].
Abul-Husn, N. S. ;
Cheng, X. ;
Li, A. H. ;
Xin, Y. ;
Schurmann, C. ;
Stevis, P. ;
Liu, Y. ;
Kozlitina, J. ;
Stender, S. ;
Wood, G. C. ;
Stepanchick, A. N. ;
Still, M. D. ;
McCarthy, S. ;
O'Dushlaine, C. ;
Packer, J. S. ;
Balasubramanian, S. ;
Gosalia, N. ;
Esopi, D. ;
Kim, S. Y. ;
Mukherjee, S. ;
Lopez, A. E. ;
Fuller, E. D. ;
Penn, J. ;
Chu, X. ;
Luo, J. Z. ;
Mirshahi, U. L. ;
Carey, D. J. ;
Still, C. D. ;
Feldman, M. D. ;
Small, A. ;
Damrauer, S. M. ;
Rader, D. J. ;
Zambrowicz, B. ;
Olson, W. ;
Murphy, A. J. ;
Borecki, I. B. ;
Shuldiner, A. R. ;
Reid, J. G. ;
Overton, J. D. ;
Yancopoulos, G. D. ;
Hobbs, H. H. ;
Cohen, J. C. ;
Gottesman, O. ;
Teslovich, T. M. ;
Baras, A. ;
Mirshahi, T. ;
Gromada, J. ;
Dewey, F. E. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 378 (12) :1096-1106
[3]   Pnpla3/Adiponutrin deficiency in mice does not contribute to fatty liver disease or metabolic syndrome [J].
Basantani, Mahesh K. ;
Sitnick, Mitch T. ;
Cai, Lingzhi ;
Brenner, Daniel S. ;
Gardner, Noah P. ;
Li, John Zhong ;
Schoiswohl, Gabriele ;
Yang, Kui ;
Kumari, Manju ;
Gross, Richard W. ;
Zechner, Rudolf ;
Kershaw, Erin E. .
JOURNAL OF LIPID RESEARCH, 2011, 52 (02) :318-329
[4]   Accumulation of PNPLA3 on lipid droplets is the basis of associated hepatic steatosis [J].
BasuRay, Soumik ;
Wang, Yang ;
Smagris, Eriks ;
Cohen, Jonathan C. ;
Hobbs, Helen H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (19) :9521-9526
[5]   The PNPLA3 Variant Associated With Fatty Liver Disease (I148M) Accumulates on Lipid Droplets by Evading Ubiquitylation [J].
BasuRay, Soumik ;
Smagris, Eriks ;
Cohen, Jonathan C. ;
Hobbs, Helen H. .
HEPATOLOGY, 2017, 66 (04) :1111-1124
[6]   SERPINA1 and HSD17B13 Gene Variants in Patients with Liver Fibrosis and Cirrhosis [J].
Basyte-Bacevice, Viktorija ;
Skieceviciene, Jurgita ;
Valantiene, Irena ;
Sumskiene, Jolanta ;
Petrenkiene, Vitalija ;
Kondrackiene, Jurate ;
Petrauskas, Dalius ;
Lammert, Frank ;
Kupcinskas, Juozas .
JOURNAL OF GASTROINTESTINAL AND LIVER DISEASES, 2019, 28 (03) :297-302
[7]   TM6SF2 and MBOAT7 Gene Variants in Liver Fibrosis and Cirrhosis [J].
Basyte-Bacevice, Viktorija ;
Skieceviciene, Jurgita ;
Valantiene, Irena ;
Sumskiene, Jolanta ;
Petrenkiene, Vitalija ;
Kondrackiene, Jurate ;
Petrauskas, Dalius ;
Lammert, Frank ;
Kupcinskas, Juozas .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (06)
[8]   Adiponutrin, a transmembrane protein corresponding to a novel dietary- and obesity-linked mRNA specifically expressed in the adipose lineage [J].
Baulande, S ;
Lasnier, F ;
Lucas, M ;
Pairault, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (36) :33336-33344
[9]   An exploratory genome-wide analysis of genetic risk for alcoholic hepatitis [J].
Beaudoin, James J. ;
Long, Nanye ;
Liangpunsakul, Suthat ;
Puri, Puneet ;
Kamath, Patrick S. ;
Shah, Vijay ;
Sanyal, Arun J. ;
Crabb, David W. ;
Chalasani, Naga P. ;
Urban, Thomas J. .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2017, 52 (11) :1263-1269
[10]   Glucokinase regulatory protein may interact with glucokinase in the hepatocyte nucleus [J].
Brown, KS ;
Kalinowski, SS ;
Megill, JR ;
Durham, SK ;
Mookhtiar, KA .
DIABETES, 1997, 46 (02) :179-186