NOTCH3 rs1043996 Polymorphism Is Associated with the Occurrence of Alcoholic Liver Cirrhosis Independently of PNPLA3 and TM6SF2 Polymorphisms

被引:2
作者
Bainrauch, Ana [1 ]
Sisl, Dino [2 ,3 ]
Markotic, Antonio [4 ,5 ]
Ostojic, Ana [6 ]
Gasparov, Slavko [7 ,8 ]
Lang, Valerija Bralic [9 ]
Kovacic, Natasa [2 ,10 ]
Grcevic, Danka [2 ,3 ]
Mrzljak, Anna [6 ,7 ]
Kelava, Tomislav [2 ,3 ]
机构
[1] Merkur Univ Hosp, Dept Internal Med, Zagreb 10000, Croatia
[2] Univ Zagreb, Croatian Inst Brain Res, Lab Mol Immunol, Zagreb 10000, Croatia
[3] Univ Zagreb, Sch Med, Dept Physiol & Immunol, Zagreb 10000, Croatia
[4] Univ Mostar, Sch Med, Dept Physiol, Mostar 88000, Bosnia & Herceg
[5] Univ Clin Hosp Mostar, Ctr Clin Pharmacol, Mostar 88000, Bosnia & Herceg
[6] Univ Zagreb, Univ Hosp Ctr Zagreb, Dept Gastroenterol & Hepatol, Zagreb 10000, Croatia
[7] Univ Zagreb, Sch Med, Zagreb 10000, Croatia
[8] Merkur Univ Hosp, Dept Pathol & Cytol, Zagreb 10000, Croatia
[9] Private Family Phys Off Zagreb, Zagreb 10000, Croatia
[10] Univ Zagreb, Sch Med, Dept Anat, Zagreb 10000, Croatia
关键词
single nucleotide polymorphisms; alcoholic liver disease; liver transplantation; hepatocellular carcinoma; Notch; PNPLA3; HEPATOCELLULAR-CARCINOMA; SIGNALING PATHWAY; RISK; SUSCEPTIBILITY; HCC;
D O I
10.3390/jcm10194621
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Alcoholic liver cirrhosis (ALC) is the most common indication for liver transplantation (LT) in Croatia and presents a risk factor for the development of hepatocellular carcinoma (HCC). However, genetic susceptibility has not yet been systematically studied. We aimed to investigate the contribution of the risk polymorphisms PNPLA3 rs738409, EGF rs4444903, TM6SF2 rs58542926, MTHFR rs1801133, previously identified in other populations and, additionally, the contribution of Notch-related polymorphisms (NOTCH1 rs3124591, NOTCH3 rs1043996 and rs1044116, NOTCH4 rs422951). The study included 401 patients. The ALC group consisted of 260 LT candidates, 128 of whom had histopathologically confirmed HCC, and 132 of whom were without HCC. The control group included 141 patients without liver disease. Genotyping was performed by PCR using Taqman assays. The patients' susceptibility to ALC was significantly associated with PNPLA3 rs738409, TM6SF2 rs58542926, and NOTCH3 rs1043996 polymorphisms. These polymorphisms remained significantly associated with ALC occurrence in a logistic regression model, even after additional model adjustment for sex and age. Cirrhotic patients with the PNPLA3 GG genotype demonstrated higher activity of ALT aminotransferases than patients with CC or CG genotypes. The susceptibility to the development of HCC in ALC was significantly associated with PNPLA3 rs738409 and EGF rs4444903 polymorphisms, and logistic regression confirmed these polymorphisms as independent predictors.
引用
收藏
页数:14
相关论文
共 39 条
[1]  
Baghdadi Ibrahim, 2020, Asian Pac J Cancer Prev, V21, P2047, DOI 10.31557/APJCP.2020.21.7.2047
[2]   The interplay of the Notch signaling in hepatic stellate cells and macrophages determines the fate of liver fibrogenesis [J].
Bansal, Ruchi ;
van Baarlen, Joop ;
Storm, Gert ;
Prakash, Jai .
SCIENTIFIC REPORTS, 2015, 5
[3]   A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis [J].
Buch, Stephan ;
Stickel, Felix ;
Trepo, Eric ;
Way, Michael ;
Herrmann, Alexander ;
Nischalke, Hans Dieter ;
Brosch, Mario ;
Rosendahl, Jonas ;
Berg, Thomas ;
Ridinger, Monika ;
Rietschel, Marcella ;
McQuillin, Andrew ;
Frank, Josef ;
Kiefer, Falk ;
Schreiber, Stefan ;
Lieb, Wolfgang ;
Soyka, Michael ;
Semmo, Nasser ;
Aigner, Elmar ;
Datz, Christian ;
Schmelz, Renate ;
Brueckner, Stefan ;
Zeissig, Sebastian ;
Stephan, Anna-Magdalena ;
Wodarz, Norbert ;
Deviere, Jacques ;
Clumeck, Nicolas ;
Sarrazin, Christoph ;
Lammert, Frank ;
Gustot, Thierry ;
Deltenre, Pierre ;
Voelzke, Henry ;
Lerch, Markus M. ;
Mayerle, Julia ;
Eyer, Florian ;
Schafmayer, Clemens ;
Cichon, Sven ;
Noethen, Markus M. ;
Nothnagel, Michael ;
Ellinghaus, David ;
Huse, Klaus ;
Franke, Andre ;
Zopf, Steffen ;
Hellerbrand, Claus ;
Moreno, Christophe ;
Franchimont, Denis ;
Morgan, Marsha Y. ;
Hampe, Jochen .
NATURE GENETICS, 2015, 47 (12) :1443-+
[4]   Targeting of the pulmonary capillary vascular niche promotes lung alveolar repair and ameliorates fibrosis [J].
Cao, Zhongwei ;
Lis, Raphael ;
Ginsberg, Michael ;
Chayez, Deebly ;
Shido, Koji ;
Rabbany, Sina Y. ;
Fong, Guo-Hua ;
Sakmar, Thomas P. ;
Rafii, Shahin ;
Ding, Bi-Sen .
NATURE MEDICINE, 2016, 22 (02) :154-162
[5]   The roles of transmembrane 6 superfamily member 2 rs58542926 polymorphism in chronic liver disease: A meta-analysis of 24,147 subjects [J].
Chen, Xinpei ;
Zhou, Pengcheng ;
Luo, De ;
Li, Bo ;
Su, Song .
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (08)
[6]   Inhibition of Notch Signaling by a γ-Secretase Inhibitor Attenuates Hepatic Fibrosis in Rats [J].
Chen, Yixiong ;
Zheng, Shaoping ;
Qi, Dan ;
Zheng, Shaojiang ;
Guo, Junli ;
Zhang, Shuling ;
Weng, Zhihong .
PLOS ONE, 2012, 7 (10)
[7]   Endothelial Notch activation reshapes the angiocrine of sinusoidal endothelia to aggravate liver fibrosis and blunt regeneration in mice [J].
Duan, Juan-Li ;
Ruan, Bai ;
Yan, Xian-Chun ;
Liang, Liang ;
Song, Ping ;
Yang, Zi-Yan ;
Liu, Yuan ;
Dou, Ke-Feng ;
Han, Hua ;
Wang, Lin .
HEPATOLOGY, 2018, 68 (02) :677-690
[8]   PNPLA3 rs738409 and TM6SF2 rs58542926 variants increase the risk of hepatocellular carcinoma in alcoholic cirrhosis [J].
Falleti, Edmondo ;
Cussigh, Annarosa ;
Cmet, Sara ;
Fabris, Carlo ;
Toniutto, Pierluigi .
DIGESTIVE AND LIVER DISEASE, 2016, 48 (01) :69-75
[9]   Hepatocellular carcinoma in cirrhosis: Incidence and risk factors [J].
Fattovich, G ;
Stroffolini, T ;
Zagni, I ;
Donato, F .
GASTROENTEROLOGY, 2004, 127 (05) :S35-S50
[10]   Hepatocellular carcinoma in the setting of alcohol-related liver disease [J].
Ganne-Carrie, Nathalie ;
Nahon, Pierre .
JOURNAL OF HEPATOLOGY, 2019, 70 (02) :284-293