Identification of autophagy-related signatures in nonalcoholic fatty liver disease and correlation with non-parenchymal cells of the liver.
Kaiwei ChenLing WeiShengnan YuNingning HeFengjuan ZhangPublished in: Molecular omics (2024)
Non-alcoholic fatty liver disease (NAFLD) is a chronic hepatic disease. The incidence and prevalence of NAFLD have increased greatly in recent years, and there is still a lack of effective drugs. Autophagy plays an important role in promoting liver metabolism and maintaining liver homeostasis, and defects in autophagy levels are considered to be related to the development of NAFLD. However, the molecular mechanisms of autophagy in NAFLD still remain unknown. In this study, we identified 6 autophagy-associated hub genes using gene expression profiles obtained from the GSE48452 and GSE89632 datasets. Biomarkers were screened according to gene significance (GS) and module membership (MM) using weighted gene co-expression network analysis (WGCNA), and the immune infiltration landscape of the liver in NAFLD patients was explored using the CIBERSORT algorithm. Subsequently, we analyzed the relationship between liver non-parenchymal cells and autophagy-related hub genes using scRNA-seq data (GSE129516). Finally, we separated the NAFLD patients into two groups based on 6 hub genes by consensus clustering and screened 10 potential autophagy-related small molecules based on the cMAP database.
Keyphrases
- endoplasmic reticulum stress
- cell death
- genome wide
- network analysis
- induced apoptosis
- signaling pathway
- bioinformatics analysis
- oxidative stress
- cell cycle arrest
- end stage renal disease
- genome wide identification
- ejection fraction
- chronic kidney disease
- copy number
- dna methylation
- magnetic resonance imaging
- peritoneal dialysis
- genome wide analysis
- magnetic resonance
- pi k akt
- transcription factor
- emergency department
- climate change
- patient reported outcomes
- contrast enhanced