Academic Journal

Bioinformatics analysis identifies potential ferroptosis key genes in the pathogenesis of diabetic peripheral neuropathy

التفاصيل البيبلوغرافية
العنوان: Bioinformatics analysis identifies potential ferroptosis key genes in the pathogenesis of diabetic peripheral neuropathy
المؤلفون: Ming Tian, Jin Yong Zhi, Fan Pan, Yong Zhu Chen, Ai Zhong Wang, Hui Ying Jia, Rong Huang, Wen Hui Zhong
المصدر: Frontiers in Endocrinology, Vol 14 (2023)
بيانات النشر: Frontiers Media S.A., 2023.
سنة النشر: 2023
المجموعة: LCC:Diseases of the endocrine glands. Clinical endocrinology
مصطلحات موضوعية: diabetic peripheral neuropathy, ferroptosis, bioinformatics, oxidative stress, immune-environment, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
الوصف: BackgroundDiabetic peripheral neuropathy (DPN) is a serious complication in Diabetes Mellitus (DM) patients and the underlying mechanism is yet unclear. Ferroptosis has been recently intensively researched as a key process in the pathogenesis of diabetes but there yet has been no related bioinformatics-based studies in the context of DPNMethodsWe used data mining and data analysis techniques to screen differentially expressed genes (DEGs) and immune cell content in patients with DPN, DM patients and healthy participants (dataset GSE95849). These DEGs were then intersected with the ferroptosis dataset (FerrDb) to obtain ferroptosis DEGs and the associated key molecules and miRNAs interactions were predicted.ResultsA total of 33 ferroptosis DEGs were obtained. Functional pathway enrichment analysis revealed 127 significantly related biological processes, 10 cellular components, 3 molecular functions and 30 KEGG signal pathways. The biological processes that were significantly enriched were in response to extracellular stimulus and oxidative stress. Key modules constructed by the protein–protein interaction network analysis led to the confirmation of the following genes of interest: DCAF7, GABARAPL1, ACSL4, SESN2 and RB1. Further miRNA interaction prediction revealed the possible involvement of miRNAs such as miR108b-8p, miR34a-5p, mir15b-5p, miR-5838-5p, miR-192-5p, miR-222-3p and miR-23c. Immune-environment content of samples between DM and DPN patients revealed significant difference in the levels of endothelial cells and fibroblasts, which further speculates their possible involvement in the pathogenesis of DPN.ConclusionOur findings could provide insight for investigations about the role of ferroptosis in the development of DPN.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1664-2392
Relation: https://www.frontiersin.org/articles/10.3389/fendo.2023.1048856/full; https://doaj.org/toc/1664-2392
DOI: 10.3389/fendo.2023.1048856
URL الوصول: https://doaj.org/article/d8384df40f2342888a3e301b5f8114a4
رقم الانضمام: edsdoj.8384df40f2342888a3e301b5f8114a4
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16642392
DOI:10.3389/fendo.2023.1048856