Bioinformatics Analysis Explores Potential Hub Genes in Nonalcoholic Fatty Liver Disease

Background: Nonalcoholic fatty liver disease (NAFLD) is now recognized as the most prevalent chronic liver disease worldwide. However, the dysregulated gene expression for NAFLD is still poorly understood.Material and methods: We analyzed two public datasets (GSE48452 and GSE89632) to identify diffe...

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Main Authors: Chutian Wu, Yun Zhou, Min Wang, Guolin Dai, Xiongxiu Liu, Leizhen Lai, Shaohui Tang
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-10-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2021.772487/full
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author Chutian Wu
Yun Zhou
Yun Zhou
Min Wang
Guolin Dai
Xiongxiu Liu
Leizhen Lai
Shaohui Tang
author_facet Chutian Wu
Yun Zhou
Yun Zhou
Min Wang
Guolin Dai
Xiongxiu Liu
Leizhen Lai
Shaohui Tang
author_sort Chutian Wu
collection DOAJ
description Background: Nonalcoholic fatty liver disease (NAFLD) is now recognized as the most prevalent chronic liver disease worldwide. However, the dysregulated gene expression for NAFLD is still poorly understood.Material and methods: We analyzed two public datasets (GSE48452 and GSE89632) to identify differentially expressed genes (DEGs) in NAFLD. Then, we performed a series of bioinformatics analyses to explore potential hub genes in NAFLD.Results: This study included 26 simple steatosis (SS), 34 nonalcoholic steatohepatitis (NASH), and 13 healthy controls (HC). We observed 6 up- and 19 down-regulated genes in SS, and 13 up- and 19 down-regulated genes in NASH compared with HC. Meanwhile, the overlapping pathways between SS and NASH were PI3K-Akt signaling pathway and pathways in cancer. Then, we screened out 10 hub genes by weighted Gene Co-Expression Network Analysis (WGCNA) and protein-protein interaction (PPI) networks. Eventually, we found that CYP7A1/GINS2/PDLIM3 were associated with the prognosis of hepatocellular carcinoma (HCC) in the TCGA database.Conclusion: Although further validation is still needed, we provide useful and novel information to explore the potential candidate genes for NAFLD prognosis and therapeutic options.
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spelling doaj.art-2d0053aeecd34dff87ebf9a877e084de2022-12-21T18:37:27ZengFrontiers Media S.A.Frontiers in Genetics1664-80212021-10-011210.3389/fgene.2021.772487772487Bioinformatics Analysis Explores Potential Hub Genes in Nonalcoholic Fatty Liver DiseaseChutian Wu0Yun Zhou1Yun Zhou2Min Wang3Guolin Dai4Xiongxiu Liu5Leizhen Lai6Shaohui Tang7Department of Gastroenterology, The First Affiliated Hospital, Jinan University, Guangzhou, ChinaDepartment of Gastroenterology, The First Affiliated Hospital, Jinan University, Guangzhou, ChinaDepartment of Gastroenterology, The First Affiliated Hospital, Gannan Medical University, Ganzhou, ChinaDepartment of Gastroenterology, The First Affiliated Hospital, Jinan University, Guangzhou, ChinaDepartment of Gastroenterology, The First Affiliated Hospital, Jinan University, Guangzhou, ChinaDepartment of Gastroenterology, The First Affiliated Hospital, Jinan University, Guangzhou, ChinaDepartment of Gastroenterology, The First Affiliated Hospital, Jinan University, Guangzhou, ChinaDepartment of Gastroenterology, The First Affiliated Hospital, Jinan University, Guangzhou, ChinaBackground: Nonalcoholic fatty liver disease (NAFLD) is now recognized as the most prevalent chronic liver disease worldwide. However, the dysregulated gene expression for NAFLD is still poorly understood.Material and methods: We analyzed two public datasets (GSE48452 and GSE89632) to identify differentially expressed genes (DEGs) in NAFLD. Then, we performed a series of bioinformatics analyses to explore potential hub genes in NAFLD.Results: This study included 26 simple steatosis (SS), 34 nonalcoholic steatohepatitis (NASH), and 13 healthy controls (HC). We observed 6 up- and 19 down-regulated genes in SS, and 13 up- and 19 down-regulated genes in NASH compared with HC. Meanwhile, the overlapping pathways between SS and NASH were PI3K-Akt signaling pathway and pathways in cancer. Then, we screened out 10 hub genes by weighted Gene Co-Expression Network Analysis (WGCNA) and protein-protein interaction (PPI) networks. Eventually, we found that CYP7A1/GINS2/PDLIM3 were associated with the prognosis of hepatocellular carcinoma (HCC) in the TCGA database.Conclusion: Although further validation is still needed, we provide useful and novel information to explore the potential candidate genes for NAFLD prognosis and therapeutic options.https://www.frontiersin.org/articles/10.3389/fgene.2021.772487/fullnonalcoholic fatty liver diseasenonalcoholic steatohepatitisdifferentially expressed geneshepatocellular carcinomabioinformatics analysis
spellingShingle Chutian Wu
Yun Zhou
Yun Zhou
Min Wang
Guolin Dai
Xiongxiu Liu
Leizhen Lai
Shaohui Tang
Bioinformatics Analysis Explores Potential Hub Genes in Nonalcoholic Fatty Liver Disease
Frontiers in Genetics
nonalcoholic fatty liver disease
nonalcoholic steatohepatitis
differentially expressed genes
hepatocellular carcinoma
bioinformatics analysis
title Bioinformatics Analysis Explores Potential Hub Genes in Nonalcoholic Fatty Liver Disease
title_full Bioinformatics Analysis Explores Potential Hub Genes in Nonalcoholic Fatty Liver Disease
title_fullStr Bioinformatics Analysis Explores Potential Hub Genes in Nonalcoholic Fatty Liver Disease
title_full_unstemmed Bioinformatics Analysis Explores Potential Hub Genes in Nonalcoholic Fatty Liver Disease
title_short Bioinformatics Analysis Explores Potential Hub Genes in Nonalcoholic Fatty Liver Disease
title_sort bioinformatics analysis explores potential hub genes in nonalcoholic fatty liver disease
topic nonalcoholic fatty liver disease
nonalcoholic steatohepatitis
differentially expressed genes
hepatocellular carcinoma
bioinformatics analysis
url https://www.frontiersin.org/articles/10.3389/fgene.2021.772487/full
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