Bioinformatics Analysis of Lactylation-related Biomarkers and Potential Pathogenesis Mechanisms in Age-Related Macular Degeneration
Background: Lactylation is increasingly recognized to play a crucial role in human health and diseases. However, its involvement in age-related macular degeneration (AMD) remains largely unclear. Objectives: The aim of this study was to identify and characterize the pivotal lactylation-related genes...
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Published in | Current genomics Vol. 26; no. 3; pp. 191 - 209 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United Arab Emirates
Bentham Science Publishers
01.01.2025
Benham Science Publishers |
Subjects | |
Online Access | Get full text |
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Summary: | Background: Lactylation is increasingly recognized to play a crucial role in human health and diseases. However, its involvement in age-related macular degeneration (AMD) remains largely unclear.
Objectives: The aim of this study was to identify and characterize the pivotal lactylation-related genes and explore their underlying mechanism in AMD.
Methods: Gene expression profiles of AMD patients and control individuals were obtained and integrated from the GSE29801 and GSE50195 datasets. Differentially expressed genes (DEGs) were screened and intersected with lactylation-related genes for lactylation-related DEGs. Machine learning algorithms were used to identify hub genes associated with AMD. Subsequently, the selected hub genes were subject to correlation analysis, and reverse transcription quantitative real-time PCR (RT-qPCR) was used to detect the expression of hub genes in AMD patients and healthy control individuals.
Results: A total of 68 lactylation-related DEGs in AMD were identified, and seven genes, including HMGN2, TOP2B, HNRNPH1, SF3A1, SRRM2, HIST1H1C, and HIST1H2BD were selected as key genes. RT-qPCR analysis validated that all 7 key genes were down-regulated in AMD patients.
Conclusion: We identified seven lactylation-related key genes potentially associated with the progression of AMD, which might deepen our understanding of the underlying mechanisms involved in AMD and provide clues for the targeted therapy. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1389-2029 1875-5488 |
DOI: | 10.2174/0113892029291661241114055924 |