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MBOAT7 rs641738 variant and hepatocellular carcinoma in non-cirrhotic individuals

Authors :
Paula Iruzubieta
Luca Miele
Salvatore Petta
Benedetta Donati
Anna Ludovica Fracanzani
Misti Vanette McCain
Stefano Ginanni Corradini
Stefania Grimaudo
Paola Dongiovanni
Giorgio Soardo
Stefano Romeo
Massimo Colombo
Antonio Grieco
Chiara Rosso
Alessio Aghemo
Renato Romagnoli
Helen L. Reeves
Ester Vanni
Laura De Luca
Luca Valenti
Rosellina Margherita Mancina
Fabio Colli
Quentin M. Anstee
Flaminia Ferri
Antonio Craxì
S. Maier
Marica Meroni
Elisabetta Bugianesi
Silvia Fargion
Donati, B.
Dongiovanni, P.
Romeo, S.
Meroni, M.
Mccain, M.
Miele, L.
Petta, S.
Maier, S.
Rosso, C.
De Luca, L.
Vanni, E.
Grimaudo, S.
Romagnoli, R.
Colli, F.
Ferri, F.
Mancina, R.
Iruzubieta, P.
Craxi, A.
Fracanzani, A.
Grieco, A.
Corradini, S.
Aghemo, A.
Colombo, M.
Soardo, G.
Bugianesi, E.
Reeves, H.
Anstee, Q.
Fargion, S.
Valenti, L.
Source :
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017), Scientific Reports
Publication Year :
2017
Publisher :
Nature Portfolio, 2017.

Abstract

Nonalcoholic fatty liver disease (NAFLD) represents an emerging cause of hepatocellular carcinoma (HCC), especially in non-cirrhotic individuals. The rs641738 C > T MBOAT7/TMC4 variant predisposes to progressive NAFLD, but the impact on hepatic carcinogenesis is unknown. In Italian NAFLD patients, the rs641738 T allele was associated with NAFLD-HCC (OR 1.65, 1.08–2.55; n = 765), particularly in those without advanced fibrosis (p PNPLA3, TM6SF2, and MBOAT7 risk variants was associated with NAFLD-HCC independently of clinical factors (p MBOAT7 rs641738 T allele is associated with reduced MBOAT7 expression and may predispose to HCC in patients without cirrhosis, suggesting it should be evaluated in future prospective studies aimed at stratifying NAFLD-HCC risk.

Details

Language :
English
ISSN :
20452322
Volume :
7
Issue :
1
Database :
OpenAIRE
Journal :
Scientific Reports
Accession number :
edsair.doi.dedup.....57462b1464ed49b80b436a6ecceb1e7f