为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Integrating TCGA and Single-Cell Sequencing Data for Hepatocellular Carcinoma: A Novel Glycosylation (GLY)/Tumor Microenvironment (TME) Classifier to Predict Prognosis and Immunotherapy Response.
Integrating TCGA and Single-Cell Sequencing Data for Hepatocellular Carcinoma: A Novel Glycosylation (GLY)/Tumor Microenvironment (TME) Classifier to Predict Prognosis and Immunotherapy Response.
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肝细胞癌(HCC)是主要的肝癌亚型。研究表明,HCC 中TIL(肿瘤浸润淋巴细胞)(TILs)的存在与较好的预后相关。然而,驱动肿瘤微环境(TME)中免疫细胞变异的分子通路仍知之甚少。糖基化(GLY)相关基因在包括 HCC 在内的多种肿瘤发病机制中具有重要功能。
本研究旨在基于糖基化相关基因评分和肿瘤微环境评分构建 GLY/TME 分类器,以提供一种新的预后模型来改善临床结局的预测。使用受试者工作特征(ROC)和生存分析评估了特征标签的可靠性,并通过外部数据集进行了验证。
此外,还研究了糖基化相关基因与免疫环境中其他细胞的相关性、GLY/TME 分类器的免疫特征以及免疫治疗的疗效。基于免疫相关分子和癌细胞信号机制的显著差异,GLY 评分低/TME 评分高亚组显示出良好的预后和治疗反应。
我们评估了 GLY/TME 分类器的预后作用,该分类器在治疗前对预后和治疗反应具有总体预后意义,这可能为患者制定最佳治疗方案提供新的选择。
The major liver cancer subtype is hepatocellular carcinoma (HCC). Studies have indicated that a better prognosis is related to the presence of tumor-infiltrating lymphocytes (TILs) in HCC.
However, the molecular pathways that drive immune cell variation in the tumor microenvironment (TME) remain poorly understood. Glycosylation (GLY)-related genes have a vital function in the pathogenesis of numerous tumors, including HCC.
This study aimed to develop a GLY/TME classifier based on glycosylation-related gene scores and tumor microenvironment scores to provide a novel prognostic model to improve the prediction of clinical outcomes. The reliability of the signatures was assessed using receiver operating characteristic (ROC) and survival analyses and was verified with external datasets.
Furthermore, the correlation between glycosylation-related genes and other cells in the immune environment, the immune signature of the GLY/TME classifier, and the efficacy of immunotherapy were also investigated. The GLY score low/TME score high subgroup showed a favorable prognosis and therapeutic response based on significant differences in immune-related molecules and cancer cell signaling mechanisms.
We evaluated the prognostic role of the GLY/TME classifier that demonstrated overall prognostic significance for prognosis and therapeutic response before treatment, which may provide new options for creating the best possible therapeutic approaches for patients.
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