AUTHOR=Li Xiaoya , Zhong Shaoping , Sun Yifan , Huang Xinmei , Li Yue , Wang Lihong , Wu Yueyue , Yang Min , Yuan Hai-Xin , Liu Jun , Zang Shufei 

TITLE=Integration analysis identifies the role of metallothionein in the progression from hepatic steatosis to steatohepatitis

JOURNAL=Frontiers in Endocrinology

VOLUME=13

YEAR=2022

URL=https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2022.951093

DOI=10.3389/fendo.2022.951093

ISSN=1664-2392

ABSTRACT=<sec><title>Background</title><p>Non-alcoholic fatty liver disease (NAFLD), a metabolic disorder that develops from non-alcoholic fatty liver (NAFL) to non-alcoholic steatohepatitis (NASH), has become an epidemic of chronic liver dysfunction worldwide. However, mechanisms that govern the transition from NAFL to NASH have not been fully elucidated.</p></sec><sec><title>Methods</title><p>Gene expression profile data of NAFLD liver tissues were obtained from Gene Expression Omnibus (GEO), including three microarray datasets with 60 NAFL and 44 NASH patients. Integrative differentially expressed genes (DEGs) between NAFL and NASH patients were identified using robust rank aggregation (RRA) analysis. Hub genes were identified combined with gene ontology functional annotation and protein–protein interaction network construction and validated using a sequencing dataset. Huh-7 cells with palmitate-induced lipid overload and NAFLD-diet mouse model of different stages were used to verify our findings.</p></sec><sec><title>Results</title><p>RRA analysis determined 70 robust DEGs between NAFL and NASH. The most robustly upregulated genes were <italic>SPP1</italic>, <italic>AKR1B10</italic>, <italic>CHST9</italic>, and <italic>ANXA2</italic>, while the most robustly downregulated DEGs were <italic>SNORD94</italic>, <italic>SCARNA10</italic>, <italic>SNORA20</italic>, and <italic>MT1M</italic>. Cellular response to zinc ion (GO: 0071294) ranked first in GO analysis of downregulated genes, and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment showed that mineral absorption (hsa04978) was significantly enriched. The involvement of the metallothionein pathway was further validated by the decrease of <italic>Mt1</italic> expression during NAFL to NASH progression in NAFLD mice and the protection from lipotoxicity in liver cells by overexpressing MT1M.</p></sec><sec><title>Conclusions</title><p>Our integrated analysis identified novel gene signatures and provided comprehensive molecular mechanisms underlying the transition from NAFL to NASH. Metallothionein might be a potential intervention target for NAFLD progression.</p></sec>