Identification of genes related to fatty acid metabolism in type 2 diabetes mellitus

被引:1
作者
Yang, Ji [1 ,2 ]
Zhou, Yikun [2 ]
Zhang, Jiarui [1 ,2 ]
Zheng, Yongqin [2 ]
He, Jundong [1 ,2 ]
机构
[1] Kunming Univ Sci & Technol, Med Sch, Kunming, Yunnan, Peoples R China
[2] Kunming Univ Sci & Technol, Peoples Hosp Yunnan Prov 1, Affiliated Hosp, Dept Endocrinol & Metab, Kunming, Yunnan, Peoples R China
关键词
Type 2 diabetes mellitus; Fatty acid metabolism; Biomarkers for T2DM; TRANSCRIPTION FACTOR SOX4; INSULIN-SECRETION; WIDE ASSOCIATION; PVT1; NEPHROPATHY; PROLIFERATION; FIBROSIS; DISEASE; VARIANT; INJURY;
D O I
10.1016/j.bbrep.2024.101849
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
Aim: Fatty acid metabolism is pivotal for lipid synthesis, cellular signaling, and maintaining cell membrane integrity. However, its diagnostic significance in type 2 diabetes mellitus (T2DM) remains unclear. Materials and methods: Three datasets and fatty acid metabolism-related genes were retrieved. Differential expression analysis, WGCNA, machine learning algorithms, diagnostic analysis, and validation were employed to identify key feature genes. Functional analysis, ceRNA network construction, immune microenvironment assessment, and drug prediction were conducted to explore the underlying molecular mechanisms. Results: Six feature genes were identified with strong diagnostic performance and were involved in processes such as ribosome function and fatty acid metabolism. Immune cells, including dendritic cells, eosinophils, and neutrophils, may play a role in the progression of T2DM. ceRNA and drug-target network analysis revealed potential interactions, such as RP11-miR-29a-YTHDF3 and BPA-MSANTD1. The expression patterns of the feature genes, except for YTHDF3, were consistently upregulated in T2DM, aligning with trends observed in the training set. Conclusion: This study investigated the potential molecular mechanisms of six fatty acid metabolism-related genes in T2DM, offering valuable insights that may guide future research and therapeutic development.
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页数:13
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