CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Significance of CD8(+) T cell infiltration-related biomarkers and the corresponding prediction model for the prognosis of kidney renal clear cell carcinoma.
Significance of CD8(+) T cell infiltration-related biomarkers and the corresponding prediction model for the prognosis of kidney renal clear cell carcinoma.
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表达细胞表面CD8的细胞毒性T细胞在包括肾透明细胞癌(KIRC)在内的抗癌免疫治疗中发挥关键作用。本研究全面分析并评估CD8+ T细胞相关标志物对KIRC患者的意义。研究考察KIRC中的免疫细胞应答,识别肿瘤浸润CD8+ T细胞(TIL-CD8T)中特异性细胞标志物及相关通路,并通过评估预后效能和不同水平下的组间差异,探索这些标志物在TIL-CD8+ T细胞中的预后特征。泛癌分析发现,CD8+ T细胞中63个上调基因有12个、396个下调基因有162个与生存预后显著相关。基于多个数据集的多平台整合分析,研究构建了一个针对TIL-CD8T的六基因风险评分模型。模型显示,TIL-CD8特征评分高与拷贝数变异发生率较高及对索拉非尼药物敏感性相关。此外,即使患者免疫检查点基因表达水平相同或相近,TIL-CD8特征评分仍能区分其预后。
Cytotoxic T cells expressing cell surface CD8 played a key role in anti-cancer immunotherapy, including kidney renal clear cell carcinoma (KIRC).
Here we set out to comprehensively analyze and evaluate the significance of CD8 + T cell-related markers for patients with KIRC.
We checked immune cell response in KIRC and identified cell type-specific markers and related pathways in the tumor-infiltrating CD8 + T (TIL-CD8T) cells.
We used these markers to explore their prognostic signatures in TIL-CD8 + T by evaluating their prognostic efficacy and group differences at various levels. Through pan-cancer analysis, 12 of 63 up-regulated and 162 of 396 down-regulated genes in CD8+ T cells were found to be significantly correlated with the survival prognosis.
Based on our highly integrated multi-platform analyses across multiple datasets, we constructed a 6-gene risk scoring model specific to TIL-CD8T. In this model, high TIL-CD8 sig score was corresponding to a higher incidence frequency of copy number variation and drug sensitivity to sorafenib.
Moreover, the prognosis of patients with the same or similar immune checkpoint gene levels could be distinguished from each other by TIL-CD8 sig score.
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