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基于代谢途径表型的肝细胞癌新型预后标志物

Novel Prognostic Signatures of Hepatocellular Carcinoma Based on Metabolic Pathway Phenotypes.

作者信息

Ye Tingbo, Lin Leilei, Cao Lulu, Huang Weiguo, Wei Shengzhe, Shan Yunfeng, Zhang Zhongjing

机构信息

Department of Hepatobiliary Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

Key Laboratory of Diagnosis and Treatment of Severe Hepato-Pancreatic Diseases of Zhejiang Province, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.

出版信息

Front Oncol. 2022 May 23;12:863266. doi: 10.3389/fonc.2022.863266. eCollection 2022.

Abstract

Hepatocellular carcinoma is a disastrous cancer with an aberrant metabolism. In this study, we aimed to assess the role of metabolism in the prognosis of hepatocellular carcinoma. Ten metabolism-related pathways were identified to classify the hepatocellular carcinoma into two clusters: Metabolism_H and Metabolism_L. Compared with Metabolism_L, patients in Metabolism_H had lower survival rates with more mutated TP53 genes and more immune infiltration. Moreover, risk scores for predicting overall survival based on eleven differentially expressed metabolic genes were developed by the least absolute shrinkage and selection operator (LASSO)-Cox regression model in The Cancer Genome Atlas (TCGA) dataset, which was validated in the International Cancer Genome Consortium (ICGC) dataset. The immunohistochemistry staining of liver cancer patient specimens also identified that the 11 genes were associated with the prognosis of liver cancer patients. Multivariate Cox regression analyses indicated that the differentially expressed metabolic gene-based risk score was also an independent prognostic factor for overall survival. Furthermore, the risk score (AUC = 0.767) outperformed other clinical variables in predicting overall survival. Therefore, the metabolism-related survival-predictor model may predict overall survival excellently for HCC patients.

摘要

肝细胞癌是一种具有异常代谢的灾难性癌症。在本研究中,我们旨在评估代谢在肝细胞癌预后中的作用。确定了10条与代谢相关的途径,将肝细胞癌分为两个簇:代谢_H和代谢_L。与代谢_L相比,代谢_H中的患者生存率较低,TP53基因发生更多突变,免疫浸润也更多。此外,通过最小绝对收缩和选择算子(LASSO)-Cox回归模型在癌症基因组图谱(TCGA)数据集中开发了基于11个差异表达代谢基因的预测总生存的风险评分,并在国际癌症基因组联盟(ICGC)数据集中进行了验证。肝癌患者标本的免疫组织化学染色也表明这11个基因与肝癌患者的预后相关。多变量Cox回归分析表明,基于差异表达代谢基因的风险评分也是总生存的独立预后因素。此外,风险评分(AUC = 0.767)在预测总生存方面优于其他临床变量。因此,代谢相关的生存预测模型可能对肝癌患者的总生存具有出色的预测能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/9168273/850e46c862ce/fonc-12-863266-g001.jpg

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