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Cited 3 time in webofscience Cited 1 time in scopus
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Functional study of acetaldehyde dehydrogenase 1 (ALDH1) in keratinocytes: microarray integrating bioinformatics approaches

Authors
Yin, SJ[Yin, Shang-Jun]Park, MW[Park, Min-Woo]Lee, BN[Lee, Bit-Na]Yang, JM[Yang, Jun-Mo]Park, YD[Park, Yong-Doo]Qian, GY[Qian, Guo-Ying]
Issue Date
31-Mar-2021
Publisher
TAYLOR & FRANCIS INC
Keywords
ALDH1; keratinocytes; microarray; antibody array; PPI maps
Citation
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, v.39, no.6, pp.2133 - 2151
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS
Volume
39
Number
6
Start Page
2133
End Page
2151
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/7491
DOI
10.1080/07391102.2020.1745281
ISSN
0739-1102
Abstract
The function of acetaldehyde dehydrogenase 1 (ALDH1) has been gradually elucidated in several diseases, especially in various cancers. However, the role of ALDH1 in skin-related diseases has been mostly unknown. Previously, we found that ALDH1 is involved in the pathogenesis of atopic dermatitis (AD). In this study, we used high-throughput screening (HTS) approaches to identify critical factors associated with ALDH1 in human keratinocytes to reveal its functions in skin. We overexpressed ALDH1 in human HaCaT keratinocytes and then conducted serial HTS studies, a DNA microarray and antibody array integrated with bioinformatics algorithms. Together, those tests identified several novel genes associated with the function of ALDH1 in keratinocytes, as well as AD, including CTSG and CCL11. In particular, GNB3, GHSR, TAS2R9, FFAR1, TAS2R16, CCL21, GPR32, NPFFR1, GPR15, FBXW12, CCL19, EDNRA, FFAR3, and RXFP3 proteins were consistently detected as hub proteins in the PPI maps. By integrating the datasets obtained from these HTS studies and using the strengths of each method, we obtained new insights into the functional role of ALDH1 in skin keratinocytes. The approach used here could contribute to the clinical understanding of ALDH1-associated applications for the treatment of AD. Communicated by Ramaswamy H. Sarma
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