Ma Shuxiao, Zhou Lu, Liu Yi, Jie Hui, Yi Min, Guo Chenglin, Mei Jiandong, Li Chuan, Zhu Lei, Deng Senyi
Department of Thoracic Surgery and Institute of Thoracic Oncology, West China Hospital, Sichuan University, Chengdu, China.
PLoS One. 2025 May 27;20(5):e0322130. doi: 10.1371/journal.pone.0322130. eCollection 2025.
This study aims to evaluate the efficacy of chemotherapy and optimize treatment strategies for patients with advanced ovarian cancer.
Based on The Cancer Genome Atlas (TCGA) transcriptome data, we conducted correlation and Bayesian network analyses to identify key genes strongly associated with chemotherapy prognosis. Reverse Transcription Quantitative Polymerase Chain Reaction (RT-qPCR) was used to verify the expression of these key genes. The Chemotherapy Benefit Index (CBI) was developed using these genes via multivariable Cox regression analysis, and validated using both internal and external validation sets (GSE32062 and GSE30161) with a random forest model. Subsequently, we analyzed distinct molecular characteristics and explored additional immunotherapy in CBI-high and CBI-low subgroups.
Based on the network and machine learning analyses, CBI was developed from the following ten genes: COL6A3, SPI1, HSF1, CD3E, PIK3R4, MZB1, FERMT3, GZMA, PSMB9 and RSF1. Significant differences in overall survival were observed among the CBI-high, medium, and low subgroups (P < 0.001), which were consistent with the two external validation sets (P < 0.001 and P = 0.003). The AUC of internal validation and two external validation cohorts were 0.87, 0.71 and 0.70, respectively. Molecular function analysis indicated that the CBI-low subgroup is characterized by the activation of cancer-related signaling pathways, immune-related biological processes, higher TP53 mutation rate, particularly with a better response to immune checkpoint blockade (ICB) treatment, while the CBI-high subgroup is characterized by inhibition of cell cycle, less response to ICB treatment, and potential therapeutic targets.
This study provided a novel CBI for patients with advanced ovarian cancer through network analyses and machine learning. CBI could serve as a prognostic prediction tool for patients with advanced ovarian cancer, and also as a potential indicator for immunotherapy.
本研究旨在评估化疗对晚期卵巢癌患者的疗效并优化治疗策略。
基于癌症基因组图谱(TCGA)转录组数据,我们进行了相关性和贝叶斯网络分析,以确定与化疗预后密切相关的关键基因。采用逆转录定量聚合酶链反应(RT-qPCR)验证这些关键基因的表达。通过多变量Cox回归分析,利用这些基因构建化疗获益指数(CBI),并使用随机森林模型在内部和外部验证集(GSE32062和GSE30161)中进行验证。随后,我们分析了不同的分子特征,并在CBI高和CBI低亚组中探索了额外的免疫治疗方法。
基于网络和机器学习分析,CBI由以下十个基因构建而成:COL6A3、SPI1、HSF1、CD3E、PIK3R4、MZB1、FERMT3、GZMA、PSMB9和RSF1。在CBI高、中、低亚组之间观察到总生存期存在显著差异(P < 0.001),这与两个外部验证集的结果一致(P < 0.001和P = 0.003)。内部验证和两个外部验证队列的AUC分别为0.87、0.71和0.70。分子功能分析表明,CBI低亚组的特征是癌症相关信号通路激活、免疫相关生物学过程、较高的TP53突变率,特别是对免疫检查点阻断(ICB)治疗反应较好,而CBI高亚组的特征是细胞周期抑制、对ICB治疗反应较小以及潜在的治疗靶点。
本研究通过网络分析和机器学习为晚期卵巢癌患者提供了一种新的CBI。CBI可作为晚期卵巢癌患者的预后预测工具,也可作为免疫治疗的潜在指标。