RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Machine learning-derived natural killer cell signature predicts prognosis and therapeutic response in clear cell renal cell carcinoma.
Machine learning-derived natural killer cell signature predicts prognosis and therapeutic response in clear cell renal cell carcinoma.
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研究描绘了 NK 细胞与各类细胞亚群之间复杂的信号相互作用,并阐明了 NK 细胞的发育轨迹。
NK 细胞与患者预后和治疗应答相关,在肿瘤免疫微环境中发挥关键作用,可能成为肾细胞癌潜在的新型预测生物标志物。
从癌症基因组图谱(TCGA)数据库获取透明细胞肾细胞癌转录组及相应临床数据,从基因表达综合数据库(GEO)获取单细胞测序数据。整合10种不同机器学习算法,建立101种组合模型。选择平均C指数最高的模型开展后续分析,并采用列线图、时间依赖性受试者工作特征(ROC)分析和Kaplan-Meier生存分析进行评估。研究比较高低风险组的免疫浸润比例、临床病理特征,以及对不同靶向治疗和免疫治疗的应答。此外,采用qRT-PCR、免疫组织化学(IHC)、克隆形成实验、CCK-8检测和流式细胞术,在本研究患者样本和肾癌细胞系中探究ARHGAP9的表达模式及功能。
共鉴定出156个NK细胞相关基因和5,189个预后相关基因,其中36个交集基因具有预后价值。采用CoxBoost联合plsRcox建立包含18个基因的风险模型,可准确预测透明细胞肾细胞癌患者预后。风险评分与肿瘤恶性程度及免疫细胞浸润显著相关。此外,结合肿瘤突变负荷和风险评分可能进一步提高临床结局预测准确性。高风险组患者更可能对靶向治疗应答,但对免疫治疗无应答。
研究描绘了NK细胞与多种细胞亚群间复杂的信号互作,并阐明NK细胞发育轨迹。所建立的NK细胞相关风险模型可提供可靠的预后信息,并识别更可能从治疗中获益的患者。
Natural killer cells, interconnected with patient prognosis and treatment response, play a pivotal role in the tumor immune microenvironment and may serve as potential novel predictive biomarkers for renal cell carcinoma.
Clear cell renal cell carcinoma transcriptome data and the corresponding clinical data were obtained from the Cancer Genome Atlas (TCGA) database. Single-cell sequencing data were sourced from the Gene Expression Omnibus (GEO) database. A risk model was established by integrating ten different machine learning algorithms, which resulted in 101 combined models. The model with the highest average C-index was selected for further analysis, and was assessed using nomogram, time-dependent receiver operating characteristics (ROC) and Kaplan-Meier survival analysis. The differences in immune infiltration fractions, clinicopathological features, and response to various targeted therapies and immunotherapy between high- and low-risk groups were investigated. Furthermore, qRT-PCR, IHC, colony formation test, CCK8 assay and flow cytometry were conducted to explore the expression pattern and function of ARHGAP9 in our own patient samples and renal cancer cell lines.
Totally, 156 NK cell-related genes and 5189 prognosis-related genes were identified, and 36 genes of their intersection demonstrated prognostic value. A risk model with 18 genes was established by Coxboost plus plsRcox, which can accurately predict the prognosis of ccRCC patients. Significant correlations were determined between risk score and tumor malignancy and immune cell infiltration. Meanwhile, a combination of tumor mutation burden plus risk score could have higher accuracy of predicting clinical outcomes. Moreover, high-risk group patients were more likely to be responsive to targeted therapy but show no response to immunotherapy.
Intricate signaling interactions between NK cells and various cellular subgroups were depicted and the developmental trajectory of NK cells was elucidated. A NK cells-related risk model was established, which can provide reliable prognostic information and identified patients with more probability of benefiting from therapy.
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