Document Type
Article
Publication Date
3-1-2021
Abstract
Objective: Accumulating evidence suggests the critical role of autophagy in the pathogenesis of diabetic retinopathy (DR). In the current study, we aim to identify autophagy genes involved in DR via microarray analyses.
Methods: Gene microarrays were performed to identify differentially expressed lncRNAs/mRNAs between normal and DR retinas. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses of lncRNA-coexpressed mRNAs were used to determine the related pathological pathways and biological modules. Real-time polymerase chain reactions (PCR) were conducted to validate the microarray analyses.
Results: A total of 2474 significantly dysregulated lncRNAs and 959 differentially expressed mRNAs were identified in the retina of DR. Based upon Signalnet analysis, Bcl2, Gabarapl2, Atg4c, and Atg16L1 participated the process of cell death in DR. Moreover, real-time PCR revealed significant upregulation of Atg16L1.
Conclusion: This study indicated the importance and potential role of Atg16L1, one of the autophagy genes, as a biomarker in DR development and progression.
Recommended Citation
Gao, Xinxiao; Du, Yunhui; Lau, Wayne Bond; Li, Yu; Zhu, Siquan; and Ma, Xin-Liang, "Atg16L1 as a Novel Biomarker and Autophagy Gene for Diabetic Retinopathy." (2021). Department of Emergency Medicine Faculty Papers. Paper 134.
https://jdc.jefferson.edu/emfp/134
Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.
PubMed ID
33791389
Language
English
Comments
This is the final full text article from the Journal of Diabetes Research, Volume 2021, Article ID 5398645,
The full text is also available at the journal's webiste: https://doi.org/10.1155/2021/5398645
Copyright. The Authors.