Chen Jie, Chen Bo, Zhu Mengli, Huang Yin, Ning Shu, Li Jinze, Li Jin, Chen Zeyu, Wang Puze, Ran Biao, Yang Jiahao, Wei Qiang, Ai Jianzhong, Liu Liangren, Cao Dehong
Oncol Res Treat. 2025 Sep 8:1-20. doi: 10.1159/000548124.
Clear cell renal cell carcinoma (ccRCC) is the most common subtype of kidney cancer and is associated with poor prognosis in advanced stages. This study aims to develop a prognostic model for patients with ccRCC based on a lysosome-related gene signature.
The clinical and transcriptomic data of Kidney Renal Clear Cell Carcinoma (KIRC) patients were downloaded from TCGA, cBioportal and GEO databases, and lysosome-related gene sets were acquired in the previous study. TCGA data was used as a training set to investigate the prognostic role of lysosomal-related genes in ccRCC, and cBioportal and GEO databases were used for validation. After the lysosome-related differentially expressed genes were found, machine learning method was used to construct a risk model, and Kaplan-Meier (K-M) and receiver operating characteristic curves (ROC) were used to evaluate the performance of the model.
Machine learning methods were utilized to identify seven gene signatures related to lysosome, which accurately predict the prognosis of ccRCC. Patients with higher risk scores demonstrate poorer overall survival (HR: 2.467, 95%CI: 1.642-3.706, P<0.001), and significant disparities in immune infiltration, immune score, and response to anticancer drugs are observed between the high-risk group and the low-risk group (P<0.001).
The prognostic model developed in this study demonstrates a high efficacy in accurately predicting the overall survival (OS) of ccRCC patients, thereby offering a novel perspective for the advancement of ccRCC treatment.
透明细胞肾细胞癌(ccRCC)是最常见的肾癌亚型,晚期预后较差。本研究旨在基于溶酶体相关基因特征开发一种ccRCC患者的预后模型。
从TCGA、cBioportal和GEO数据库下载肾透明细胞癌(KIRC)患者的临床和转录组数据,并在前一项研究中获取溶酶体相关基因集。将TCGA数据用作训练集,以研究溶酶体相关基因在ccRCC中的预后作用,并使用cBioportal和GEO数据库进行验证。在发现溶酶体相关差异表达基因后,采用机器学习方法构建风险模型,并使用Kaplan-Meier(K-M)曲线和受试者工作特征曲线(ROC)评估模型性能。
利用机器学习方法鉴定出7个与溶酶体相关的基因特征,可准确预测ccRCC的预后。风险评分较高的患者总生存期较差(HR:2.467,95%CI:1.642-3.706,P<0.001),高风险组和低风险组在免疫浸润、免疫评分和抗癌药物反应方面存在显著差异(P<0.001)。
本研究开发的预后模型在准确预测ccRCC患者的总生存期(OS)方面显示出高效性,从而为ccRCC治疗的进展提供了新的视角。