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免疫相关风险预后模型在透明细胞肾细胞癌中的应用:对免疫治疗的启示。

Immune-related risk prognostic model for clear cell renal cell carcinoma: Implications for immunotherapy.

机构信息

Clinical Medical College of Weifang Medical University, Weifang, China.

Department of Oncology, People's Hospital of Rizhao, Rizhao, China.

出版信息

Medicine (Baltimore). 2023 Aug 25;102(34):e34786. doi: 10.1097/MD.0000000000034786.

DOI:10.1097/MD.0000000000034786
PMID:37653791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10470711/
Abstract

Clear cell renal cell carcinoma (ccRCC) is associated with complex immune interactions. We conducted a comprehensive analysis of immune-related differentially expressed genes in patients with ccRCC using data from The Cancer Genome Atlas and ImmPort databases. The immune-related differentially expressed genes underwent functional and pathway enrichment analysis, followed by COX regression combined with LASSO regression to construct an immune-related risk prognostic model. The model comprised 4 IRGs: CLDN4, SEMA3G, CAT, and UCN. Patients were stratified into high-risk and low-risk groups based on the median risk score, and the overall survival rate of the high-risk group was significantly lower than that of the low-risk group, confirming the reliability of the model from various perspectives. Further comparison of immune infiltration, tumor mutation load, and immunophenoscore (IPS) comparison between the 2 groups indicates that the high-risk group could potentially demonstrate a heightened sensitivity towards immunotherapy checkpoints PD-1, CTLA-4, IL-6, and LAG3 in ccRCC patients. The proposed model not only applies to ccRCC but also shows potential in developing into a prognostic model for renal cancer, thus introducing a novel approach for personalized immunotherapy in ccRCC.

摘要

透明细胞肾细胞癌(ccRCC)与复杂的免疫相互作用有关。我们使用来自癌症基因组图谱(TCGA)和 ImmPort 数据库的数据,对 ccRCC 患者的免疫相关差异表达基因进行了全面分析。对免疫相关差异表达基因进行了功能和通路富集分析,然后进行 COX 回归和 LASSO 回归相结合构建免疫相关风险预后模型。该模型包含 4 个 IRGs:CLDN4、SEMA3G、CAT 和 UCN。根据中位数风险评分将患者分为高风险组和低风险组,高风险组的总生存率明显低于低风险组,从多个角度验证了模型的可靠性。进一步比较两组之间的免疫浸润、肿瘤突变负荷和免疫表型评分(IPS),表明高风险组在 ccRCC 患者中对免疫检查点 PD-1、CTLA-4、IL-6 和 LAG3 可能具有更高的敏感性。该模型不仅适用于 ccRCC,而且在开发肾肿瘤的预后模型方面也具有潜力,从而为 ccRCC 的个性化免疫治疗提供了一种新方法。

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本文引用的文献

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Mediators Inflamm. 2023 Apr 4;2023:1075265. doi: 10.1155/2023/1075265. eCollection 2023.
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CDK4/6 inhibition triggers ICAM1-driven immune response and sensitizes LKB1 mutant lung cancer to immunotherapy.CDK4/6 抑制触发 ICAM1 驱动的免疫反应,并使 LKB1 突变型肺癌对免疫治疗敏感。
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Computational construction of TME-related lncRNAs signature for predicting prognosis and immunotherapy response in clear cell renal cell carcinoma.
肾细胞癌中的细胞应激与皮肤表现——一篇叙述性综述
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基于 TME 相关 lncRNAs 的计算构建用于预测透明细胞肾细胞癌的预后和免疫治疗反应的标志物。
J Clin Lab Anal. 2022 Aug;36(8):e24582. doi: 10.1002/jcla.24582. Epub 2022 Jul 8.
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Urocortin stimulates ERK1/2 phosphorylation and proliferation but reduces ATP production of MCF7 breast cancer cells.尿皮质素可刺激 ERK1/2 磷酸化和增殖,但减少 MCF7 乳腺癌细胞的 ATP 生成。
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