Department of Obstetrics and Gynecology, Institute of Medical Genetics, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Med Sci Monit. 2009 Dec;15(12):SR22-8.
The search for gene candidates in multifactorial diseases such as sarcoidosis can be based on the integration of linkage association data, gene expression data, and protein profile data from genomic, transcriptomic and proteomic studies, respectively.
MATERIAL/METHODS: In this study we performed a literature-based search for studies reporting such data, followed by integration of collected information. Different databases were examined--Medline, HugGE Navigator, ArrayExpress and Gene Expression Omnibus (GEO). Candidate genes were defined as genes which were reported in at least 2 different types of omics studies. Genes previously investigated in sarcoidosis were excluded from further analyses.
We identified 177 genes associated with sarcoidosis as potential new candidate genes. Subsequently, 9 gene candidates identified to overlap in 2 different types of studies (genomic, transcriptomic and/or proteomic) were consistently reported in at least 3 studies: SERPINB1, FABP4, S100A8, HBEGF, IL7R, LRIG1, PTPN23, DPM2 and NUP214. These genes are involved in regulation of immune response, cellular proliferation, apoptosis, inhibition of protease activity, lipid metabolism. Exact biological functions of HBEGF, LRIG1, PTPN23, DPM2 and NUP214 remain to be completely elucidated.
We propose 9 candidate genes: SERPINB1, FABP4, S100A8, HBEGF, IL7R, LRIG1, PTPN23, DPM2 and NUP214, as genes with high potential for association with sarcoidosis.
在结节病等多因素疾病中,基因候选物的寻找可以基于整合连锁关联数据、基因表达数据和来自基因组、转录组和蛋白质组学研究的蛋白质谱数据。
材料/方法:在这项研究中,我们进行了基于文献的研究报告,随后整合了收集的信息。检查了不同的数据库 - Medline、HugGE Navigator、ArrayExpress 和基因表达综合 (GEO)。候选基因被定义为至少在 2 种不同类型的组学研究中报告的基因。先前在结节病中研究过的基因被排除在进一步的分析之外。
我们确定了 177 个与结节病相关的基因作为潜在的新候选基因。随后,在至少 3 项研究中一致报道了在 2 种不同类型的研究(基因组、转录组和/或蛋白质组学)中重叠的 9 个候选基因:SERPINB1、FABP4、S100A8、HBEGF、IL7R、LRIG1、PTPN23、DPM2 和 NUP214。这些基因参与免疫反应、细胞增殖、细胞凋亡、抑制蛋白酶活性、脂质代谢的调节。HBEGF、LRIG1、PTPN23、DPM2 和 NUP214 的确切生物学功能仍有待完全阐明。
我们提出了 9 个候选基因:SERPINB1、FABP4、S100A8、HBEGF、IL7R、LRIG1、PTPN23、DPM2 和 NUP214,作为与结节病高度相关的基因。