Y. Murakami, K. Kanda, K. Yokota, H. Kanayama, S. Kagawa
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引用次数: 18
摘要
我们的目的是阐明“免疫蛋白体”在肾细胞癌(RCC)中的临床作用,它参与了主要组织相容性复合体(MHC) i类限制性抗原呈递系统的加速途径。使用RT-PCR分析研究了54例rcc中6个蛋白体亚基(现有的X、Y和Z亚基以及免疫蛋白体亚基LMP7、LMP2和MECL1)的相对表达,并与包括患者预后在内的临床病理指标进行了比较。LMP7和LMP2基因在高级别肿瘤中表达明显低,LMP7和MECL1基因在高级别肿瘤中表达明显低。低水平的LMP7、LMP2和MECL1表达与缩短生存期密切相关(LMP7: P = 0.0002, LMP2: P < 0.0001, MECL1: P < 0.0047)。亚单位X、Y和Z的水平与这些测量无显著相关。这些发现表明,低水平的免疫蛋白体亚基表达的rcc在其抗原呈递系统中存在障碍。因此,它们可能会逃避免疫监视并使患者预后恶化。
Prognostic significance of immuno-proteosome subunit expression in patients with renal-cell carcinoma: a preliminary study.
Our purpose was to elucidate the clinical roles of the "immuno-proteosome," which is involved in the accelerated pathway of the major histocompatibility complex (MHC) class I-restricted antigen presentation system, in renal cell carcinoma (RCC). The relative expression of six proteosome subunits (existing subunits X, Y, and Z and immunoproteosome subunits LMP7, LMP2, and MECL1) in 54 RCCs was investigated using RT-PCR analysis and was compared with clinicopathological measures, including patient outcome. Expression of the LMP7 and LMP2 genes was significantly low in high-grade tumors, and that of the LMP7 and MECL1 genes was significantly low in high-stage tumors. Low levels of LMP7, LMP2, and MECL1 expression were strongly associated with shortened survival (LMP7: P = 0.0002, LMP2: P < 0.0001, MECL1: P < 0.0047). The levels of subunits X, Y, and Z had no significant correlation with those measures. These findings suggest that RCCs with low level of immuno-proteosome subunit expression have a disorder in their antigen-presentation system. As a consequence, they may escape from immune surveillance and worsen patient outcome.