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用于胃癌预后预测的代谢相关基因特征的开发与验证

Development and validation of metabolism-related gene signature in prognostic prediction of gastric cancer.

作者信息

Luo Tianqi, Li Yuanfang, Nie Runcong, Liang Chengcai, Liu Zekun, Xue Zhicheng, Chen Guoming, Jiang Kaiming, Liu Ze-Xian, Lin Huan, Li Cong, Chen Yingbo

机构信息

Department of Gastric Surgery, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, China.

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou 510060, China.

出版信息

Comput Struct Biotechnol J. 2020 Oct 17;18:3217-3229. doi: 10.1016/j.csbj.2020.09.037. eCollection 2020.

Abstract

Gastric cancer is one of the most common malignant tumours in the world. As one of the crucial hallmarks of cancer reprogramming of metabolism and the relevant researches have a promising application in the diagnosis treatment and prognostic prediction of malignant tumours. This study aims to identify a group of metabolism-related genes to construct a prediction model for the prognosis of gastric cancer. A large cohort of gastric cancer cases (1121 cases) from public database was included in our analysis and classified patients into training and testing cohorts at a ratio of 7: 3. After identifying a list of metabolism-related genes having prognostic value, we constructed a risk score based on metabolism-related genes using LASSO-COX method. According to the risk score, patients were divided into high- and low-risk groups. Our results revealed that high-risk patients had a significantly worse prognosis than low-risk patients in both the training (high-risk vs low-risk patients; five years overall survival: 37.2% vs 72.2%;  < 0.001) and testing cohorts (high-risk vs low-risk patients; five years overall survival: 42.9% vs 62.9%;  < 0.001). This observation was validated in the external validation cohort (high-risk vs. low-risk patients; five years overall survival: 30.2% vs 40.4%;  = 0.007). To reinforce the predictive ability of the model, we integrated risk score, age, adjuvant chemotherapy, and TNM stage into a nomogram. According to the result of receiver operating characteristic curves and decision curves analysis, we found that the nomogram score had a superior predictive ability than conventional factors, indicating that the risk score combined with clinicopathological features can develop a robust prediction for survival and improve the individualized clinical decision making of the patient. In conclusion, we identified a list of metabolic genes related to survival and developed a metabolism-based predictive model for gastric cancer. Through a series of bioinformatics and statistical analyses, the predictive ability of the model was confirmed.

摘要

胃癌是世界上最常见的恶性肿瘤之一。作为癌症代谢重编程的关键特征之一,相关研究在恶性肿瘤的诊断、治疗及预后预测方面具有广阔的应用前景。本研究旨在识别一组与代谢相关的基因,构建胃癌预后预测模型。我们的分析纳入了来自公共数据库的一大组胃癌病例(1121例),并按7:3的比例将患者分为训练组和测试组。在确定了一组具有预后价值的代谢相关基因后,我们使用LASSO-COX方法基于这些基因构建了风险评分。根据风险评分,将患者分为高风险组和低风险组。我们的结果显示,在训练组(高风险组与低风险组患者;五年总生存率:37.2%对72.2%;<0.001)和测试组(高风险组与低风险组患者;五年总生存率:42.9%对62.9%;<0.001)中,高风险患者的预后均显著差于低风险患者。这一观察结果在外部验证队列中得到了验证(高风险组与低风险组患者;五年总生存率:30.2%对40.4%;=0.007)。为了增强模型的预测能力,我们将风险评分、年龄、辅助化疗和TNM分期整合到一个列线图中。根据受试者工作特征曲线和决策曲线分析结果,我们发现列线图评分比传统因素具有更强的预测能力,这表明风险评分结合临床病理特征能够对生存情况做出可靠的预测,并改善患者的个体化临床决策。总之,我们识别出了一组与生存相关的代谢基因,并构建了基于代谢的胃癌预测模型。通过一系列生物信息学和统计分析,证实了该模型的预测能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfee/7649605/d64735dbfe0e/ga1.jpg

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