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碳水化合物代谢相关模型的建立与验证及其在肝癌患者预后与免疫图谱预测中的价值

Development and Validation of a Carbohydrate Metabolism-Related Model for Predicting Prognosis and Immune Landscape in Hepatocellular Carcinoma Patients.

机构信息

Department of Oncology, The First Affiliated Hospital of Nanchang University, Nanchang, 330006, China.

Jiangxi Institute of Respiratory Disease, The First Affiliated Hospital of Nanchang University, Nanchang, 330006, China.

出版信息

Curr Med Sci. 2024 Aug;44(4):771-788. doi: 10.1007/s11596-024-2886-y. Epub 2024 Aug 3.

Abstract

OBJECTIVE

The activities and products of carbohydrate metabolism are involved in key processes of cancer. However, its relationship with hepatocellular carcinoma (HCC) is unclear.

METHODS

The cancer genome atlas (TCGA)-HCC and ICGC-LIRI-JP datasets were acquired via public databases. Differentially expressed genes (DEGs) between HCC and control samples in the TCGA-HCC dataset were identified and overlapped with 355 carbohydrate metabolism-related genes (CRGs) to obtain differentially expressed CRGs (DE-CRGs). Then, univariate Cox and least absolute shrinkage and selection operator (LASSO) analyses were applied to identify risk model genes, and HCC samples were divided into high/low-risk groups according to the median risk score. Next, gene set enrichment analysis (GSEA) was performed on the risk model genes. The sensitivity of the risk model to immunotherapy and chemotherapy was also explored.

RESULTS

A total of 8 risk model genes, namely, G6PD, PFKFB4, ACAT1, ALDH2, ACYP1, OGDHL, ACADS, and TKTL1, were identified. Moreover, the risk score, cancer status, age, and pathologic T stage were strongly associated with the prognosis of HCC patients. Both the stromal score and immune score had significant negative/positive correlations with the risk score, reflecting the important role of the risk model in immunotherapy sensitivity. Furthermore, the stromal and immune scores had significant negative/positive correlations with risk scores, reflecting the important role of the risk model in immunotherapy sensitivity. Eventually, we found that high-/low-risk patients were more sensitive to 102 drugs, suggesting that the risk model exhibited sensitivity to chemotherapy drugs. The results of the experiments in HCC tissue samples validated the expression of the risk model genes.

CONCLUSION

Through bioinformatic analysis, we constructed a carbohydrate metabolism-related risk model for HCC, contributing to the prognosis prediction and treatment of HCC patients.

摘要

目的

碳水化合物代谢的活性和产物参与了癌症的关键过程。然而,其与肝细胞癌(HCC)的关系尚不清楚。

方法

通过公共数据库获取癌症基因组图谱(TCGA)-HCC 和 ICGC-LIRI-JP 数据集。在 TCGA-HCC 数据集中,鉴定 HCC 和对照样本之间的差异表达基因(DEGs),并与 355 个碳水化合物代谢相关基因(CRGs)重叠,以获得差异表达的 CRGs(DE-CRGs)。然后,应用单变量 Cox 和最小绝对值收缩和选择算子(LASSO)分析来识别风险模型基因,并根据中位风险评分将 HCC 样本分为高/低风险组。接下来,对风险模型基因进行基因集富集分析(GSEA)。还探讨了风险模型对免疫治疗和化疗的敏感性。

结果

共鉴定出 8 个风险模型基因,即 G6PD、PFKFB4、ACAT1、ALDH2、ACYP1、OGDHL、ACADS 和 TKTL1。此外,风险评分、癌症状态、年龄和病理 T 期与 HCC 患者的预后密切相关。基质评分和免疫评分与风险评分均呈显著负/正相关,反映了风险模型在免疫治疗敏感性中的重要作用。此外,基质和免疫评分与风险评分呈显著负/正相关,反映了风险模型在免疫治疗敏感性中的重要作用。最终,我们发现高/低风险患者对 102 种药物更敏感,提示风险模型对化疗药物具有敏感性。HCC 组织样本的实验结果验证了风险模型基因的表达。

结论

通过生物信息学分析,我们构建了一个与 HCC 相关的碳水化合物代谢相关风险模型,有助于预测 HCC 患者的预后和治疗。

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