γδ T 细胞调节小细胞肺癌中的抗肿瘤免疫
γδ T cells modulate anti-tumor immunity in small cell lung cancer.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Development of a prognostic signature based on anoikis-related genes in hepatocellular carcinoma with the utilization of LASSO-cox method.
Development of a prognostic signature based on anoikis-related genes in hepatocellular carcinoma with the utilization of LASSO-cox method.
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构建基于失巢凋亡相关基因(ARGs)的预后特征模型,用于预测肝细胞癌(HCC)患者的预后,并阐明其涉及的分子机制。
本研究应用生物信息学算法,整合并分析了来自癌症基因组图谱和国际癌症基因组联盟数据库的777例HCC RNA-seq样本。通过最小绝对收缩和选择算子-cox回归方法构建预后特征模型。为评估该特征模型预测事件的准确性,采用了多种技术手段,如Kaplan-Meier生存曲线、受试者工作特征曲线分析、列线图构建以及单因素和多因素Cox回归研究。我们分别使用基因集富集分析和CIBERSORT R包研究了该特征模型潜在的分子生物学机制和免疫机制。同时,利用从人类蛋白质图谱获取的免疫组化染色结果,验证了参与预后特征模型的核心基因的差异表达水平。
我们构建了一个包含5个ARGs的HCC预后特征模型,并在测试队列和验证队列中成功评估和验证了其预后价值。由该预后特征模型计算得出的风险评分被证明是总生存期的独立不良预后因素。建立了一套基于风险评分的列线图,并发现其在预测OS方面有效。对潜在分子生物学机制和免疫机制的进一步研究表明,该特征模型可能与肿瘤中的代谢失调和gamma delta T细胞浸润有关。
失巢凋亡相关预后特征模型可预测HCC患者的生存预后,并为个体化HCC治疗提供了有价值的参考。
To develop a signature based on anoikis-related genes (ARGs) for predicting the prognosis of patients with hepatocellular carcinoma (HCC), and to elucidate the molecular mechanisms involved. In this study, bioinformatic algorithms were applied to integrate and analyze 777 HCC RNA-seq samples from the cancer genome atlas and international cancer genome consortium repositories.
A prognostic signature was developed via the least absolute shrinkage and selection operator-cox regression method. To evaluate the accuracy of the signature in predicting events, multi-type technical means, such as Kaplan-Meier plots, receiver operating characteristic curve analysis, nomogram construction, and univariate and multivariate Cox regression studies were performed.
We investigated the underlying molecular biological mechanisms and immune mechanisms of the signature using gene set enrichment analysis and the CIBERSORT R package, respectively. Meanwhile, immunohistochemical staining acquired from the human protein atlas was used to confirm the differential expression levels of hub genes involved in the prognostic signature.
We developed an HCC prognostic signature with a collection of 5 ARGs, and the prognostic value was successfully assessed and verified in both the test and validation cohorts. The risk scores calculated by the prognostic signature were proved to be an independent negative prognostic factor for overall survival. A set of nomograms based on risk scores was established and found to be effective in predicting OS.
Further investigation of the underlying molecular biological mechanisms and immune mechanisms indicated that the signature may be relevant to metabolic dysregulation and infiltration of gamma delta T cells in the tumor. The survival prognosis of HCC patients can be predicted by the anoikis-related prognostic signature, and it serves as a valuable reference for individualized HCC therapy.
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