Bioinformatics-based analysis of the relationship between plasminogen regulatory genes and photoaging
- PMID: 38634239
- DOI: 10.1111/jocd.16266
Bioinformatics-based analysis of the relationship between plasminogen regulatory genes and photoaging
Abstract
Background: Ultraviolet radiation causes skin photoaging by producing a variety of enzymes, which impact both skin health and hinder beauty. Currently, the early diagnosis and treatment of photoaging remain a challenge. Bioinformatics analysis has strong advantages in exploring core genes and the biological pathways of photoaging.
Aims: To screen and validate key risk genes associated with plasminogen in photoaging and to identify potential target genes for photoaging.
Methods: Two human transcriptome datasets were obtained by searching the Gene Expression Omnibus (GEO) database, and the mRNAs in the GSE131789 dataset were differentially analyzed, and then the weighted gene co-expression network analysis (WGCNA) was performed to find out the strongest correlations. Template genes, interaction analysis of differentially expressed genes (DEGs), modular genes with the most WGCNA correlations, and genecard database genes related to plasminogen were performed, and further Kyoto genes and Genome Encyclopedia (KEGG) pathway analysis. Two different algorithms, least absolute shrinkage and selection operator (LASSO) and support vector machines-recursive feature elimination (SVM-RFE), were used to find key genes. Then the data set (GSE206495) was validated and analyzed. Real-time PCR was performed to validate the expression of key genes through in vitro cellular experiments.
Results: IFI6, IFI44L, HRSP12, and BMP4 were screened from datasets as key genes for photoaging and further analysis showed that these genes have significant diagnostic value for photoaging.
Conclusion: IFI6, IFI44L, HRSP12, and BMP4 play a key role in the pathogenesis of photoaging, and serve as promising potential predictive biomarkers for photoaging.
Keywords: UV; bioinformatics analysis; gene; photoaging; plasminogen.
© 2024 The Authors. Journal of Cosmetic Dermatology published by Wiley Periodicals LLC.
References
REFERENCES
-
- Kammeyer A, Luiten RM. Oxidation events and skin aging. Ageing Res Rev. 2015;21:16‐29. doi:10.1016/j.arr.2015.01.001
-
- Han S, Liu P, Yan Q, et al. Seawater pearl hydrolysate inhibits photoaging via decreasing oxidative stress, autophagy and apoptosis of ultraviolet B‐induced human skin keratinocytes. J Cosmet Dermatol. 2023;23(1):256‐270. doi:10.1111/jocd.15916
-
- Kim H, Jang J, Song MJ, et al. Inhibition of matrix metalloproteinase expression by selective clearing of senescent dermal fibroblasts attenuates ultraviolet‐induced photoaging. Biomed Pharmacother. 2022;150:113034. doi:10.1016/j.biopha.2022.113034
-
- Amano S. Characterization and mechanisms of photoageing‐related changes in skin. Damages of basement membrane and dermal structures. Exp Dermatol. 2016;25(Suppl 3):14‐19. doi:10.1111/exd.13085
-
- IIriyama S, Yasuda M, Nishikawa S, Takai E, Hosoi J, Amano S. Decrease of laminin‐511 in the basement membrane due to photoaging reduces epidermal stem/progenitor cells. Sci Rep. 2020;10(1):12592. doi:10.1038/s41598-020-69558-y
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
