Genome-wide transcriptional profiling of chronic cutaneous lupus erythematosus (CCLE) peripheral blood identifies systemic alterations relevant to the skin manifestation

被引:27
作者
Dey-Rao, R. [1 ]
Sinha, A. A. [1 ]
机构
[1] SUNY Buffalo, Dept Dermatol, Buffalo, NY 14203 USA
关键词
Microarray; Cutaneous lupus; Blood; Gene-expression; Interferon; Apoptosis; GENE-EXPRESSION; DISEASE-ACTIVITY; INTERFERON-ALPHA; RHEUMATOID-ARTHRITIS; MONONUCLEAR-CELLS; ASIAN POPULATIONS; ALOPECIA-AREATA; SOLUBLE CD14; ASSOCIATION; SERUM;
D O I
10.1016/j.ygeno.2014.11.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Major gaps remain regarding pathogenetic mechanisms underlying clinical heterogeneity in lupus erythematosus (LE). As systemic changes are likely to underlie skin specific manifestation, we analyzed global gene expression in peripheral blood of a small cohort of chronic cutaneous LE (CCLE) patients and healthy individuals. Unbiased hierarchical clustering distinguished patients fromcontrols revealing a "disease" based signature. Functional annotation of the differentially expressed genes (DEGs) highlight enrichment of interferon related immune response and apoptosis signatures, along with other key pathways. There is a 26% overlap of the blood and lesional skin transcriptional profile from a previous analysis by our group. We identified four transcriptional "hot spots" at chromosomal regions harboring statistically increased numbers of DEGs which offer prioritized potential loci for downstream fine mapping studies in the search for CCLE specific susceptibility loci. Additionally, we uncover evidence to support both shared and distinct mechanisms for cutaneous and systemic manifestations of lupus. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:90 / 100
页数:11
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