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Tumor microenvironment immune subtypes for classification of novel clear cell renal cell carcinoma profiles with prognostic and therapeutic implications

机译:肿瘤微环境免疫亚型,用于分类新型透明细胞肾细胞癌细胞,具有预后和治疗意义

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ABSTRACT:Currently, no effective prognostic model of clear cell renal cell carcinoma (ccRCC) based on immune cell infiltration has been developed. Recent studies have identified 6 immune groups (IS) in 33 solid tumors. We aimed to characterize the expression pattern of IS in ccRCC and evaluate the potential in predicting patient prognosis. The clinical information, immune subgroup, somatic mutation, copy number variation, and methylation score of patients with TCGA ccRCC cohort were downloaded from UCSC Xena for further analysis. The most dominant IS in ccRCC was the inflammatory subgroup (immune C3) (86.5%), regardless of different pathological stages, pathological grades, and genders. In the C3 subgroup, stage IV (69.1%) and grade 4 (69.9%) were the least presented. Survival analysis showed that the IS could effectively predict the overall survival (OS) (P??.0001) and disease-specific survival (DSS) (P??.0001) of ccRCC alone, of which group C3 (OS, HR?=?2.3, P??.001; DSS, HR?=?2.84, P??.001) exhibited the best prognosis. Among the most frequently mutated ccRCC genes, only VHL and PBRM1 were found to be common in the C3 group. The homologous recombination deficiency score was also lower. High heterogeneity was observed in immune cells and immunoregulatory genes of IS. Notably, CD4 memory resting T cells were highly infiltrating, regulatory T cells (Treg) showed low infiltration, and most immunoregulatory genes (such as CX3CL1, IFNA2, TLR4, SELP, HMGB1, and TNFRSF14) were highly expressed in the C3 subgroup than in other subgroups. Enrichment analysis showed that adipogenesis, apical junction, hypoxia, IL2 STAT5 signaling, TGF-beta signaling, and UV response DN were activated, whereas E2F targets, G2M checkpoint, and MYC targets V2 were downregulated in the C3 group. Immune classification can more accurately classify ccRCC patients and predict OS and DSS. Thus, IS-based classification may be a valuable tool that enables individualized treatment of patients with ccRCC.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:摘要:目前,已经开发了基于免疫细胞浸润的透明细胞肾细胞癌(CCRCC)的有效预后模型。最近的研究已经确定了33种实体瘤中的6种免疫基团(是)。我们的目标是表征在CCRCC中的表达模式,并评估预测患者预后的潜力。从UCSC Xena下载了TCGA CCRCC队患者的临床信息,免疫亚组,体细胞突变,拷贝数变异和甲基化评分,以进一步分析。最常用的是CCRCC是炎症亚组(免疫C3)(86.5%),无论不同的病理阶段,病理成绩和人均。在C3亚组中,最少提出阶段IV(69.1%)和4级(69.9%)。生存分析表明,可以有效地预测整体存活(OS)(p≤0001)和单独的CCRCC的特异性存活(DSS)(P 1S)(p≤00),其中C3组( OS,HR?=?2.3,P?& 001; dss,hr?=Δ=Δ=Δ= 3. 001)表现出最佳预后。在最常突变的CCRCC基因中,发现VHL和PBRM1在C3组中常见。同源重组缺乏评分也降低。在免疫细胞中观察到高异质性,并且是IS的免疫调节基因。值得注意的是,CD4记忆静止T细胞高度浸润,调节性T细胞(Treg)显示出低浸润,并且大多数免疫导致基因(如CX3Cl1,IFNA2,TLR4,SELP,HMGB1和TNFRSF14)在C3亚组中高于C3亚组高度表达其他亚组。富集分析表明,激活脂肪生成,顶端结,缺氧,IL2 STAT5信号,TGF-β发信号和UV响应DN,而E2F靶标,G2M检查点和MYC靶标V2在C3组中下调。免疫分类可以更准确地分类CCRCC患者和预测OS和DSS。因此,基于基于的分类可以是一种有价值的工具,其能够使CCRCC.copyright患者的个体化治疗? 2021提交人。由Wolters Kluwer Health,Inc。出版

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