首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Key Immunological Functions Involved in the Progression of Epithelial Ovarian Serous Carcinoma Discovered by the Gene Ontology-Based Immunofunctionome Analysis
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Key Immunological Functions Involved in the Progression of Epithelial Ovarian Serous Carcinoma Discovered by the Gene Ontology-Based Immunofunctionome Analysis

机译:基于基因本体论的免疫功能组分析发现上皮性卵巢浆液性癌进展的关键免疫功能

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摘要

Serous carcinoma (SC) is the most common and lethal subtype of epithelial ovarian carcinoma; immunotherapy is a potential treatment for SC, however, the global immunological functions of SC as well as their change during the progression of SC have not been investigated in detail till now. We conducted a genome-wide integrative analysis to investigate the immunofunctionomes of SC at four tumor stages by quantifying the immunological functions defined by the Gene Ontology gene sets. DNA microarray gene expression profiles of 1100 SCs and 136 normal ovarian tissue controls were downloaded from the Gene Expression Omnibus database and converted to the functionome. Then the immunofunctionomes were reconstructed by extracting the offspring from the functionome for the four SC staging groups. The key immunological functions extracted from immunofunctionomes with a series of filters revealed that the immunopathy of SC consisted of a group of deregulated functions with the core members including B cell activation and differentiation, regulation of leukocyte chemotaxis/cellular extravasation, antigen receptor mediated signaling pathway, T helper mediated immunity and macrophage activation; and the auxiliary elements included leukocyte mediated immunity, regulation of inflammatory response, T cell differentiation, mononuclear cell migration, megakaryocyte differentiation, complement activation and cytokine production. These deregulated immunological functions reveal the candidates to target in the immunotherapy.
机译:浆液性癌(SC)是上皮性卵巢癌中最常见和致命的亚型。免疫疗法是SC的一种潜在治疗方法,但是,迄今为止,尚未对SC的整体免疫功能及其在SC进展过程中的变化进行详细研究。我们进行了全基因组整合分析,以通过量化由基因本体论基因组定义的免疫功能来研究SC在四个肿瘤阶段的免疫功能组。从Gene Expression Omnibus数据库下载了1100个SC和136个正常卵巢组织对照的DNA微阵列基因表达谱,并将其转换为功能组。然后通过从四个SC分期组的功能组中提取后代来重建免疫功能组。使用一系列过滤器从免疫功能组中提取的关键免疫功能表明,SC的免疫病由一组功能失调的核心成员组成,包括B细胞活化和分化,白细胞趋化性/细胞外渗调节,抗原受体介导的信号传导途径, T辅助介导的免疫和巨噬细胞激活;辅助元素包括白细胞介导的免疫,调节炎症反应,T细胞分化,单核细胞迁移,巨核细胞分化,补体激活和细胞因子产生。这些失调的免疫功能揭示了免疫疗法中靶向的候选药物。

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