基于贝叶斯网络分析的晚期卵巢癌化疗获益新指标的确定。

IF 2.9 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-05-27 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0322130
Shuxiao Ma, Lu Zhou, Yi Liu, Hui Jie, Min Yi, Chenglin Guo, Jiandong Mei, Chuan Li, Lei Zhu, Senyi Deng
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引用次数: 0

摘要

背景:本研究旨在评价晚期卵巢癌患者化疗的疗效并优化治疗策略。方法:基于癌症基因组图谱(Cancer Genome Atlas, TCGA)转录组数据,进行相关分析和贝叶斯网络分析,找出与化疗预后密切相关的关键基因。利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。利用这些基因通过多变量Cox回归分析得出化疗获益指数(Chemotherapy Benefit Index, CBI),并采用随机森林模型对内部和外部验证集(GSE32062和GSE30161)进行验证。随后,我们分析了不同的分子特征,并探索了cbi高亚组和cbi低亚组的额外免疫治疗。结果:基于网络和机器学习分析,CBI由以下10个基因开发:COL6A3、SPI1、HSF1、CD3E、PIK3R4、MZB1、FERMT3、GZMA、PSMB9和RSF1。结论: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治疗方案。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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of a novel chemotherapy benefit index for patients with advanced ovarian cancer based on Bayesian network analysis.

Background: This study aims to evaluate the efficacy of chemotherapy and optimize treatment strategies for patients with advanced ovarian cancer.

Methods: 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.

Results: 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.

Conclusions: 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.

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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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