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-based development of a cytotoxicity prediction model for NK cell therapy in cancers.
Machine learning-based development of a cytotoxicity prediction model for NK cell therapy in cancers.
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该模型为利用 NK 免疫细胞进行肿瘤精准治疗提供了工具与基础,并可能应用于临床实践。
自然杀伤(NK)细胞通过抑制性和活化性受体的综合信号介导抗肿瘤免疫。由于患者间受体-配体表达存在异质性,NK细胞过继转移疗法的疗效因人而异。本研究旨在基于受体-配体相互作用建立预测模型,评估NK细胞的治疗效果。
研究者分析NK细胞和肿瘤细胞受体-配体表达谱并评估NK细胞细胞毒性;通过数据库挖掘和实验筛选选出11对关键受体-配体,建立基于机器学习的随机森林模型。采用流式细胞术获取受体-配体表达谱,并计算每对分子的联合预测因子。使用独立数据集验证模型,并评估其在不同肿瘤类型中的通用性。
该模型具有显著预测性能,在卵巢癌队列中的准确率为84.2%,曲线下面积(AUC)为0.908。体外实验及临床样本验证了其预测能力,并揭示受体-配体表达与NK细胞杀伤效能之间存在复杂非线性相互作用。研究鉴定出癌症特异性配体表达模式。该模型在所研究癌症类型中表现最佳,对其他癌症的适用性中等,并显示出与转录组数据结合用于预测的潜力。
该模型为利用NK免疫细胞精准治疗肿瘤提供了工具和基础,也可能应用于临床实践。
Natural killer (NK) cells mediate anti-tumor immunity through integrated signaling of inhibitory and activating receptors. The efficacy of NK cell adoptive transfer therapy varies among patients due to heterogeneous receptor-ligand expression. This study aimed to develop a predictive model based on receptor-ligand interactions to determine NK cells' therapeutic effects.
Through analyses of receptor-ligand expression profiles of NK and tumor cells and assessment of NK cell cytotoxicity, we developed a machine learning-based random forest model using 11 key receptor-ligand pairs selected through database mining and experimental screening. Flow cytometry was used to obtain receptor-ligand profiles, and combined predictors were calculated for each pair. The model was validated using independent datasets and evaluated for generalizability across different tumor types.
The model showed significant predictive performance, achieving an accuracy of 84.2% and an area under the curve (AUC) of 0.908 in ovarian cancer cohorts. This predictive capability was validated in both in vitro experiments and clinical samples, revealing complex non-linear interactions between receptor-ligand expression and NK cell killing efficacy. Cancer-specific ligand expression patterns were identified. While showing optimal performance in studied cancer types, it exhibited moderate applicability to other cancers and demonstrated potential compatibility with transcriptomic data for prediction.
This model provides tools and foundations for the precise treatment of tumors using NK immune cells and may be applied in clinical practice.
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