Temporal changes in gene expression in the skin of patients treated with isotretinoin provide insight into its mechanism of action.
Publication/Presentation Date
5-1-2009
Abstract
Isotretinoin (13-cis RA) is the most potent agent in the treatment of acne. Insights into its mechanism of action can lead to drug discovery of alternative compounds with comparable efficacy but improved safety. The goal of this study is to compare the temporal changes in gene expression in the skin of acne patients after 1 week and 8 weeks of treatment with isotretinoin. Microarray analysis was performed on skin biopsies taken from eight acne patients prior to and at 8 weeks of treatment with isotretinoin. Results were compared with data obtained from seven acne patients biopsied at one week of treatment in a prior study. Distinctly different patterns of gene expression were noted. At 8 weeks, genes encoding extracellular matrix proteins were upregulated and numerous genes encoding lipid metabolizing enzymes were downregulated. At 1 week, genes encoding differentiation markers, tumor suppressors and serine proteases were upregulated. Only three genes were commonly downregulated. The temporal changes in gene expression in patient skin noted with isotretinoin substantiate many previously reported effects of isotretinoin and other retinoids, suggesting a model wherein isotretinoin induces apoptosis leading to reduced sebaceous gland size, decreased expression of lipid metabolizing enzymes and increased matrix remodeling during acne resolution.
Volume
1
Issue
3
First Page
177
Last Page
187
ISSN
1938-1980
Published In/Presented At
Nelson, A. M., Zhao, W., Gilliland, K. L., Zaenglein, A. L., Liu, W., & Thiboutot, D. M. (2009). Temporal changes in gene expression in the skin of patients treated with isotretinoin provide insight into its mechanism of action. Dermato-endocrinology, 1(3), 177–187. https://doi.org/10.4161/derm.1.3.8258
Disciplines
Medicine and Health Sciences
PubMedID
20436886
Department(s)
Department of Medicine
Document Type
Article