Machine learning-based integration identifies the ferroptosis hub genes in nonalcoholic steatohepatitis

被引:8
作者
Dai, Longfei [1 ]
Yuan, Wenkang [1 ]
Jiang, Renao [1 ]
Zhan, Zhicheng [1 ]
Zhang, Liangliang [1 ]
Xu, Xinjian [1 ]
Qian, Yuyang [1 ]
Yang, Wenqi [1 ]
Zhang, Zhen [1 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Dept Gen Surg, 218 Jixi Rd, Hefei 230022, Anhui, Peoples R China
关键词
Machine learning; Ferroptosis; NASH; ZFP36; Diagnosis; FATTY LIVER; BINDING;
D O I
10.1186/s12944-023-01988-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BackgroundFerroptosis, is characterized by lipid peroxidation of fatty acids in the presence of iron ions, which leads to cell apoptosis. This leads to the disruption of metabolic pathways, ultimately resulting in liver dysfunction. Although ferroptosis is linked to nonalcoholic steatohepatitis (NASH), understanding the key ferroptosis-related genes (FRGs) involved in NASH remains incomplete. NASH may be targeted therapeutically by identifying the genes responsible for ferroptosis.MethodsTo identify ferroptosis-related genes and develop a ferroptosis-related signature (FeRS), 113 machine-learning algorithm combinations were used.ResultsThe FeRS constructed using the Generalized Linear Model Boosting algorithm and Gradient Boosting Machine algorithms exhibited the best prediction performance for NASH. Eight FRGs, with ZFP36 identified by the algorithms as the most crucial, were incorporated into in FeRS. ZFP36 is significantly enriched in various immune cell types and exhibits significant positive correlations with most immune signatures.ConclusionZFP36 is a key FRG involved in NASH pathogenesis.
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页数:14
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