Skinomics: past, present and future for diagnostic microarray studies in dermatology

被引:9
作者
Blumenberg, Miroslav [1 ]
机构
[1] NYU, Sch Med, NYU Langone Med Ctr,RO Perelman Dept Dermatol, Dept Biochem & Mol Pharmacol,NYU Canc Inst, New York, NY 10016 USA
关键词
bioinformatics; disease markers; epidermal differentiation; melanoma; non-invasive; psoriasis; stem cells; UV damage; GENOME-WIDE ASSOCIATION; PSORIASIS SUSCEPTIBILITY LOCI; GENE-EXPRESSION PATTERNS; MERKEL CELL-CARCINOMA; HUMAN EPIDERMAL-KERATINOCYTES; NF-KAPPA-B; HUMAN SKIN; STEM-CELLS; IN-VIVO; TRANSCRIPTIONAL PROGRAM;
D O I
10.1586/14737159.2013.846827
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
Easily accessible, skin was among the first targets analyzed using omics' and dermatology embraced the approaches very early. Microarrays have been used to define disease markers, identify transcriptional changes and even trace the course of treatment. Melanoma and psoriasis have been explored using microarrays. Particularly noteworthy is the multinational mapping of psoriasis susceptibility loci. The transcriptional changes in psoriasis have been identified using hundreds of biopsies. Epidermal keratinocytes have been studied because they respond to UV light, infections, inflammatory and immunomodulating cytokines, toxins and so on. Epidermal differentiation genes are being characterized and are expressed in human epidermal stem cells. Exciting discoveries defining human skin microbiomes have opened a new field of research with great medical potential. Specific to dermatology, the non-invasive skin sampling for microarray studies, using tape stripping, has been developed; it promises to advance dermatology toward omics' techniques directly applicable to the personalized medicine of the future.
引用
收藏
页码:885 / 894
页数:10
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