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Identification of pyroptosis-related gene signature in nonalcoholic steatohepatitis.
Mao, Fei; Wang, E; Fu, Li; Fan, Wenhua; Zhou, Jing; Yan, Guofeng; Liu, Tiemin; Li, Yao.
Affiliation
  • Mao F; Ministry of Education Key Laboratory of Metabolism and Molecular Medicine, Department of Endocrinology and Metabolism, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
  • Wang E; Department of Laboratory Animal Science, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China.
  • Fu L; Department of Laboratory Animal Science, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China.
  • Fan W; Department of Laboratory Animal Science, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China.
  • Zhou J; Department of Laboratory Animal Science, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China.
  • Yan G; Department of Laboratory Animal Science, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, China.
  • Liu T; Human Phenome Institute, Fudan University, Shanghai, 200032, China. tiemin_liu@fudan.edu.cn.
  • Li Y; Key Laboratory of Genetic Engineering, School of Life Sciences, Zhongshan Hospital, Fudan University, Shanghai, 200032, China. tiemin_liu@fudan.edu.cn.
Sci Rep ; 14(1): 3175, 2024 02 07.
Article in En | MEDLINE | ID: mdl-38326642
ABSTRACT
Non-alcoholic fatty liver disease (NAFLD) has emerged as one of the major causes of liver-related morbidity and mortality globally. It ranges from simple steatosis to non-alcoholic steatohepatitis (NASH) characterized by ballooning and hepatic inflammation. In the past few years, pyroptosis has been shown as a type of programmed cell death that triggers inflammation and plays a role in the development of NASH. However, the roles of pyroptosis-related genes (PRGs) in NASH remained unclear. In this study, we studied the expression level of pyroptosis-related genes (PRGs) in NASH and healthy controls, developed a diagnostic model of NASH based on PRGs and explored the pathological mechanisms associated with pyroptosis. We further compared immune status between NASH and healthy controls, analyzed immune status in different subtypes of NASH. We identified altogether twenty PRGs that were differentially expressed between NASH and normal liver tissues. Then, a novel diagnostic model consisting of seven PRGs including CASP3, ELANE, GZMA, CASP4, CASP9, IL6 and TP63 for NASH was constructed with an area under the ROC curve (AUC) of 0.978 (CI 0.965-0.99). Obvious variations in immune status between healthy controls and NASH cases were detected. Subsequently, the consensus clustering method based on differentially expressed PRGs was constructed to divide all NASH cases into two distinct pyroptosis subtypes with different immune and biological characteristics. Pyroptosis-related genes may play an important role in NASH and can provide new insights into the diagnosis and underlying mechanisms of NASH.
Subject(s)

Full text: 1 Collection: 01-internacional Health context: 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Non-alcoholic Fatty Liver Disease Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Sci Rep Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Non-alcoholic Fatty Liver Disease Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: Sci Rep Year: 2024 Document type: Article