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:Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer.
Natural killer cell-related prognostic risk model predicts prognosis and treatment outcomes in triple-negative breast cancer.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
5-NK 细胞相关基因特征展现出卓越的预测性能,为评估免疫治疗的成功提供了新视角。它将为未来实现 TNBC 的精准和综合治疗提供新见解。
自然杀伤(NK)细胞对肿瘤的发生、识别和预后至关重要。NK细胞相关基因在肿瘤免疫微环境(TIME)和免疫治疗中的作用尚不清楚。三阴性乳腺癌(TNBC)是一种高度侵袭性的恶性肿瘤。因此,本研究旨在开发一个可靠的NK细胞相关风险模型,并为预测TNBC的预后提供一种新的系统。
从既往研究中收集NK细胞相关基因。基于TCGA和GEO数据库,采用单因素和LASSO cox回归分析建立NK细胞相关基因特征。将TNBC患者分为高风险组和低风险组。之后,进行生存分析,并基于该特征评估免疫治疗反应。此外,使用"oncoPredict" R包评估一些传统化疗药物的药物敏感性。另外,通过qRT-PCR在TNBC细胞系中验证该特征所涉及基因的表达水平。
根据5-NK细胞相关基因特征的中位风险评分,将TNBC患者分为高风险组和低风险组。低风险组与更好的临床结局相关。此外,不同风险组之间的差异表达基因富集于与免疫相关的生物学活动。发现低风险组中肿瘤免疫细胞高度浸润。根据TIDE评分和免疫检查点相关基因表达分析,低风险组的TNBC患者被提示对免疫治疗有更好的反应。最终,一些经典抗肿瘤药物在高风险组中的疗效低于低风险组。
Natural killer (NK) cells are crucial to the emergence, identification, and prognosis of cancers. The roles of NK cell-related genes in the tumor immune microenvironment (TIME) and immunotherapy treatment are unclear. Triple-negative breast cancer (TNBC) is a highly aggressive malignant tumor. Hence, this study was conducted to develop a reliable risk model related to NK cells and provide a novel system for predicting the prognosis of TNBC.
NK cell-related genes were collected from previous studies. Based on TCGA and GEO database, univariate and LASSO cox regression analysis were used to establish the NK cell-related gene signature. The patients with TNBC were separated to high-risk and low-risk groups. After that, survival analysis was conducted and the responses to immunotherapies were evaluated on the basis of the signature. Moreover, the drug sensitivity of some traditional chemotherapeutic drugs was assessed by using the "oncoPredict" R package. In addition, the expression levels of the genes involved in the signature were validated by using qRT-PCR in TNBC cell lines.
The patients with TNBC were divided into high- and low-risk groups according to the median risk score of the 5-NK cell-related gene signature. The low-risk group was associated with a better clinical outcome. Besides, the differentially expressed genes between the different risk groups were enriched in the biological activities associated with immunity. The tumor immune cells were found to be highly infiltrated in the low-risk groups. In accordance with the TIDE score and immune checkpoint-related gene expression analysis, TNBC patients in the low-risk groups were suggested to have better responses to immunotherapies. Eventually, some classical anti-tumor drugs were shown to be less effective in high-risk groups than in low-risk groups.
The 5-NK cell-related gene signature exhibit outstanding predictive performance and provide fresh viewpoints for evaluating the success of immunotherapy. It will provide new insights to achieve precision and integrated treatment for TNBC in the future.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。