Integrative transcriptome-wide analysis of atopic dermatitis for drug repositioningopen access
- Authors
- Song, Jaeseung; Kim, Daeun; Lee, Sora; Jung, Junghyun; Joo, Jong Wha J.; Jang, Wonhee
- Issue Date
- Jun-2022
- Publisher
- Nature Publishing Group
- Keywords
- Transcriptome; Atopic Dermatitis; Drug Repositioning; Genetics; Genome-wide Association Study; Human; Meta Analysis; Metabolism; Procedures; Quality Of Life; Dermatitis, Atopic; Drug Repositioning; Genome-wide Association Study; Humans; Quality Of Life; Transcriptome
- Citation
- Communications Biology, v.5, no.1, pp 1 - 13
- Pages
- 13
- Indexed
- SCIE
SCOPUS
- Journal Title
- Communications Biology
- Volume
- 5
- Number
- 1
- Start Page
- 1
- End Page
- 13
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/2946
- DOI
- 10.1038/s42003-022-03564-w
- ISSN
- 2399-3642
2399-3642
- Abstract
- Integrative genomic and transcriptomic analyses on publicly available data-sets together with in silico drug repositioning identifies alternative therapeutic options to treat atopic dermatitis. Atopic dermatitis (AD) is one of the most common inflammatory skin diseases, which significantly impact the quality of life. Transcriptome-wide association study (TWAS) was conducted to estimate both transcriptomic and genomic features of AD and detected significant associations between 31 expression quantitative loci and 25 genes. Our results replicated well-known genetic markers for AD, as well as 4 novel associated genes. Next, transcriptome meta-analysis was conducted with 5 studies retrieved from public databases and identified 5 additional novel susceptibility genes for AD. Applying the connectivity map to the results from TWAS and meta-analysis, robustly enriched perturbations were identified and their chemical or functional properties were analyzed. Here, we report the first research on integrative approaches for an AD, combining TWAS and transcriptome meta-analysis. Together, our findings could provide a comprehensive understanding of the pathophysiologic mechanisms of AD and suggest potential drug candidates as alternative treatment options.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Life Science and Biotechnology > Department of Life Science > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.