Premium
Comparisons of gene expression in normal, lesional, and non‐lesional psoriatic skin using DNA microarray techniques
Author(s) -
Xie Shaoqiong,
Chen Zhongjian,
Wang Qingliang,
Song Xun,
Zhang Linglin
Publication year - 2014
Publication title -
international journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 93
eISSN - 1365-4632
pISSN - 0011-9059
DOI - 10.1111/ijd.12476
Subject(s) - psoriasis , gene expression , gene , microarray , biopsy , pathology , medicine , dna microarray , skin biopsy , biology , immunology , genetics
Objectives This study was designed to explore the pathogenesis of psoriasis and to identify potential bio‐targets. Genome array technology was used to analyze the gene expression profiles of lesional and non‐lesional psoriatic skin samples and normal skin samples. Methods Gene expression profile GSE 14905 was downloaded from the Gene Expression Omnibus ( GEO ) database. This included skin biopsy samples from normal healthy donors ( n = 21), lesional skin biopsy samples from psoriasis patients ( n = 33), and non‐lesional skin biopsy samples from psoriasis patients ( n = 28). Differentially expressed genes ( DEG s) were identified using the Limma package in R language. Functions of specific DEG s were predicted by Gene Ontology ( GO ) enrichment analysis. A protein–protein interaction network was constructed to display the interactions among common DEG s. Finally, DAVID and WebGestalt were used to achieve a functional analysis of common DEG s. Results Totals of 1020, 562, and 643 genes, respectively, were identified as being differentially expressed in normal versus lesional, normal versus non‐lesional, and lesional versus non‐lesional samples. The specific DEG s in the three groups were enriched for several GO terms, including mitotic cell cycle , immune response , and response to organic matter . The 40 common DEG s in the three groups may be involved in the defense response pathway in the development of psoriasis. Furthermore, three genes ( RGS 1 , SOCS 3 , and NAMPT ) may play key roles in distinguishing lesional and non‐lesional tissues from normal tissues, and 10 genes ( PTRRC , ALDH 1A3 , SAMSA 1 , C15orf48 , ZC 3H12A , SOD 2 , IL 8 , LTF , RHCG , and IL 7R ) may play key roles in distinguishing non‐lesional from normal and lesional samples. Conclusions These genes may be considered as potential diagnostic markers and targets of therapeutics in psoriasis.