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杀伤细胞免疫球蛋白样受体及其配体基因与上皮性卵巢癌的相关性。

Associations between genes for killer immunoglobulin-like receptors and their ligands in patients with epithelial ovarian cancer.

机构信息

Department of Bone Marrow Transplantation and Onco-Hematology, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice Branch, Gliwice, Poland.

Department of Clinical and Experimental Oncology, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Gliwice Branch, Gliwice, Poland.

出版信息

Hum Immunol. 2014 Jun;75(6):508-13. doi: 10.1016/j.humimm.2014.04.002. Epub 2014 Apr 19.

Abstract

Killer immunoglobulin-like receptors (KIRs) regulate function of NK cells and subsets of T cells. HLA class I molecules are ligands for inhibitory KIRs while specificity of activating KIRs is mainly unknown. Both KIR and HLA genotypes are highly polymorphic. In this study we analyzed associations of KIR and KIR ligand genes with the incidence and clinical course of epithelial ovarian cancer. DNA of 142 patients was analyzed for KIR genes and 103 samples were typed for HLA class I. Control group consisted of 200 healthy individuals, including 83 women, analyzed separately. The frequency of KIR genes in patients and controls were comparable. HLA-C group 1 (ligand for KIR2DL2/3) was more frequent in patients than in controls (86.4% vs. 67.5%, p=0.002). The frequency of KIR2DS4fl was higher in patients with endometrioid cancer (72.3%) compared with other histological subtypes (36.5%, p=0.004) and controls (29.5%, p=0.0001). KIR and KIR ligand genotype did not influence significantly the clinical course of the disease. We conclude that the genotype of KIR ligands is strongly associated with the incidence of epithelial ovarian cancer while KIR2DS4fl confers susceptibility to endometrioid subtype of the disease.

摘要

杀伤细胞免疫球蛋白样受体(KIRs)调节 NK 细胞和 T 细胞亚群的功能。HLA I 类分子是抑制性 KIR 的配体,而激活性 KIR 的特异性主要未知。KIR 和 HLA 基因型均高度多态。在这项研究中,我们分析了 KIR 和 KIR 配体基因与上皮性卵巢癌的发病和临床病程的关系。对 142 例患者的 DNA 进行了 KIR 基因分析,对 103 例样本进行了 HLA I 类分型。对照组由 200 名健康个体组成,其中包括 83 名女性,单独进行分析。患者和对照组的 KIR 基因频率相似。与对照组(67.5%)相比,HLA-C 组 1(KIR2DL2/3 的配体)在患者中更为常见(86.4%,p=0.002)。与其他组织学亚型(36.5%,p=0.004)和对照组(29.5%,p=0.0001)相比,KIR2DS4fl 在子宫内膜样癌患者中更为常见。KIR 和 KIR 配体基因型并未显著影响疾病的临床病程。我们得出结论,KIR 配体的基因型与上皮性卵巢癌的发病密切相关,而 KIR2DS4fl 则使子宫内膜样亚型的疾病易感性增加。

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