Perturbation of Wnt/β‐catenin signaling and sexual dimorphism in non‐alcoholic fatty liver disease

• Published in: Hepatology research Vol. 52; no. 5; pp. 433 - 448
• Main Authors: Yeh, Matthew M, Shi, Xiuhui, Yang, Jingxuan, Li, Min, Fung, Kar‐Ming, Daoud, Sayed S.
• Format: Journal Article
• Language: English
• Published: Netherlands Wiley Subscription Services, Inc 01.05.2022
• Subjects: Catenin; Fatty liver; Genomes; Immunoblotting; Liver diseases; MalE protein; Molecular modelling; Myc protein; non‐alcoholic fatty liver disease; non‐alcoholic steatohepatitis; Polymerase chain reaction; Post-menopause; RNA‐seq; RT2‐profiler PCR arrays; Sexual dimorphism; Signal transduction; Wnt protein; Wnt/β‐catenin; RT2-profiler PCR arrays; non-alcoholic fatty liver disease; RNA-seq; Wnt/β-catenin; sexual dimorphism; non-alcoholic steatohepatitis
• ISSN: 1386-6346; 1872-034X
• DOI: 10.1111/hepr.13754

Aims The prevalence of non‐alcoholic fatty liver disease (NAFLD) and its progression to non‐alcoholic steatohepatitis (NASH) is higher in postmenopausal women than men. The aim of this study was to determine the molecular mechanisms underlying this sexual dimorphism in NAFLD. Methods A total of 24 frozen liver samples of both sexes (normal and NAFLD/NASH) were used in this study. Total RNAseq was first used to identify differentially expressed genes (DEGs) between samples. Enrichment analysis of Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and Reactome were used to analyze biological pathways. RT2 profiler polymerase chain reaction (PCR) arrays were used to identify genes associated with the biological pathways. Immunoblotting was used to validate protein expression of certain genes. Results We identified 4362 genes that are differentially expressed between NAFLD/NASH and normal samples; of those 745 genes were characterized as sex specific in NAFLD/NASH. Multiple pathway analysis platforms showed that Wnt‐signaling is a candidate shared for a common biological pathway‐associated with NAFLD/NASH. Using Wnt pathway focused PCR array we identified many genes involved in canonical pathway (Wnt/β‐catenin activation) such as CTNNB1, c‐Myc and CCND2 are overexpressed in female cases, whereas these genes are either not detected or downregulated in male cases. Immunoblot analysis validated the expression of CTNNB1 in female cases but not in male protein samples. Conclusions Our study suggests, for the first time, that the activation of canonical Wnt signaling could be one of the main pathways associated with sexual dimorphism in NAFLD and NASH.