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Integrative Analysis to Explore the Biological Association Between Environmental Skin Diseases and Ambient Particulate Matter

Overview
Journal Sci Rep
Specialty Science
Date 2022 Jun 13
PMID 35697899
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Abstract

Although numerous experimental studies have suggested a significant association between ambient particulate matter (PM) and respiratory damage, the etiological relationship between ambient PM and environmental skin diseases is not clearly understood. Here, we aimed to explore the association between PM and skin diseases through biological big data analysis. Differential gene expression profiles associated with PM and environmental skin diseases were retrieved from public genome databases. The co-expression among them was analyzed using a text-mining-based network analysis software. Activation/inhibition patterns from RNA-sequencing data performed with PM-treated normal human epidermal keratinocytes (NHEK) were overlapped to select key regulators of the analyzed pathways. We explored the adverse effects of PM on the skin and attempted to elucidate their relationships using public genome data. We found that changes in upstream regulators and inflammatory signaling networks mediated by MMP-1, MMP-9, PLAU, S100A9, IL-6, and S100A8 were predicted as the key pathways underlying PM-induced skin diseases. Our integrative approach using a literature-based co-expression analysis and experimental validation not only improves the reliability of prediction but also provides assistance to clarify underlying mechanisms of ambient PM-induced dermal toxicity that can be applied to screen the relationship between other chemicals and adverse effects.

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References
1.
Srimuruganandam B, Nagendra S . Source characterization of PM10 and PM2.5 mass using a chemical mass balance model at urban roadside. Sci Total Environ. 2012; 433:8-19. DOI: 10.1016/j.scitotenv.2012.05.082. View

2.
Kim J, Moon J, Park E, Lee K, Hong Y . Changes in oxidative stress biomarker and gene expression levels in workers exposed to volatile organic compounds. Ind Health. 2010; 49(1):8-14. DOI: 10.2486/indhealth.ms1112. View

3.
Kovaka S, Zimin A, Pertea G, Razaghi R, Salzberg S, Pertea M . Transcriptome assembly from long-read RNA-seq alignments with StringTie2. Genome Biol. 2019; 20(1):278. PMC: 6912988. DOI: 10.1186/s13059-019-1910-1. View

4.
Turovskaya O, Foell D, Sinha P, Vogl T, Newlin R, Nayak J . RAGE, carboxylated glycans and S100A8/A9 play essential roles in colitis-associated carcinogenesis. Carcinogenesis. 2008; 29(10):2035-43. PMC: 2556970. DOI: 10.1093/carcin/bgn188. View

5.
Li N, Sioutas C, Cho A, Schmitz D, Misra C, Sempf J . Ultrafine particulate pollutants induce oxidative stress and mitochondrial damage. Environ Health Perspect. 2003; 111(4):455-60. PMC: 1241427. DOI: 10.1289/ehp.6000. View