首页|肝细胞癌双硫死亡相关长链非编码RNA预后风险模型的构建与评估

肝细胞癌双硫死亡相关长链非编码RNA预后风险模型的构建与评估

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目的 探讨双硫死亡相关长链非编码RNA(DRlncRNA)在肝细胞癌(HCC)中的预后价值,构建肝细胞癌DRlncRNA的预后风险模型.方法 从TCGA数据库中下载377例HCC患者的RNA测序数据以及临床数据(包括374个HCC组织和50个癌旁组织),使"R"软件进行共表达分析确定DRlncRNA,并在癌组织及癌旁组织中进行差异性分析.预处理临床数据得到343例合格的样本,并随机分为训练集(train)172例、测试集(test)171例,在训练集中通过单因素Cox、最小绝对收缩和选择算法(LASSO)、多因素Cox分析确定预后风险模型,计算出风险评分并根据风险评分的中位值将患者分为高、低风险组;对两组患者进行生存分析并绘制受试者工作特征(ROC)曲线进行效能评估.在测试集和整个队列中验证.进一步分析高、低风险组间生物学富集通路和免疫相关功能的差异.两组间比较通过Wilcoxon检验完成.结果 提取lncRNA数据并进行共表达分析以及差异分析后共得到211个DRlncRNA,将差异分析后的DRlncRNA与临床样本合并后最终筛选出4个DRlncRNA用来构建预后风险模型,该模型中高风险组患者的生存率明显低于低风险组(P<0.05),训练集患者1年、3年和5年的生存预测性能曲线下面积(AUC)值分别为0.790、0.601、0.690.测试集和整个队列中也具有良好的预测效能.进一步分析表明高、低风险组在生物学富集通路和免疫相关功能方面差异有统计学意义(P<0.05).结论 DRlncRNA在HCC中具有较高的预后价值,且以4个DRlncRNA构建的预后风险模型可以有效预测HCC患者的生存预后.
Construction and evaluation of a prognostic risk model for hepatocellular carcinoma based on disul-fidptosis-related long non-coding RNA
Objective To investigate the prognostic value of disulfidptosis-related long non-coding RNA(DRlncRNA)in hepatocellular carcinoma(HCC)and to establish a prognostic risk model for DRlncRNA in HCC.Methods RNA sequencing data and clinical data of 377 HCC patients(including 374 HCC tissues and 50 para-cancerous tissues)were downloaded from the TCGA database,and"R"software was used for co-expression analysis to identify DRlncRNA,and differences in cancer tissues and para-can-cerous tissues were analyzed.After preprocessing clinical data,343 qualified samples were obtained,and randomly divided into a training set(train)of 172 cases and a test set(test)of 171 cases.Univariate Cox,least absolute shrinkage and selection operator(LASSO),and multivariate Cox analyses were employed to determine the prognostic risk model in the training set.Risk scores were calculated,and patients were clas-sified into high and low-risk groups based on the median risk score.Survival analysis was performed in both groups and receiver operating characteristic(ROC)curves were plotted to evaluate efficacy.The test set and the entire queue were validated.Further analysis explored biological enrichment pathways and differ-ences in immune-related functions between high and low-risk groups.The comparison between the two groups was performed by Wilcoxon test.Results A total of 211 DRlncRNAs were obtained after lncRNA data were extracted and co-expression analysis and difference analysis were performed.After combining the DRlncRNAs after difference analysis with clinical samples,4 DRlncRNAs were finally selected to build a prognostic risk model.In this model,the survival rate of high-risk group was significantly lower than that of low-risk group(P<0.05).The area under curve(AUC)values of 1-year,3-year and 5-year survival pre-diction for patients in the training set were 0.790,0.601 and 0.690,respectively.It also had good predic-tive performance in the test set and the whole queue.Further analysis showed that the high and low risk groups also had statistically significant difference in biological enrichment pathway and immune-related functions(P<0.05).Conclusion DRlncRNA has high prognostic value in HCC,and the prognostic risk model constructed with four DRlncRNA can effectively predict the survival prognosis of HCC patients.

Hepatocellular carcinomaLong non-coding RNADisulfidptosisPrognosis

郝定盈、肖俊豪、庹云、裴捷、黄杰钰、苑伟、吴帆、王百林

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贵州医科大学临床医学院,贵阳 550004

暨南大学附属广州红十字会医院普通外科,广州 510220

肝细胞癌 双硫死亡 长链非编码RNA 预后

国家自然科学基金广东省自然科学基金

819744422020A1515010799

2024

中华实验外科杂志
中华医学会

中华实验外科杂志

CSTPCD
影响因子:0.759
ISSN:1001-9030
年,卷(期):2024.41(4)
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