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基于TCGA数据的早期和晚期肝细胞癌免疫浸润的预后分析及生物标志物鉴定

Prognostic Analysis and Biomarkers Identification of Immune Infiltration in Early and Late Stage Hepatocellular Carcinoma Based on TCGA Data.

作者信息

Jiang Wenying, Wang Yunxing, Yu Changtao, Sui Deling, Du Gang, Li Youchun

机构信息

Department of General Surgery, The Second People's Hospital of Liaocheng Affiliated to Shandong First Medical University, Liaocheng, Shandong, People's Republic of China.

Department of General Surgery, Qilu Hospital of Shandong University, Jinan, Shandong, People's Republic of China.

出版信息

Int J Gen Med. 2023 Jun 16;16:2519-2530. doi: 10.2147/IJGM.S420458. eCollection 2023.

Abstract

BACKGROUND

Hepatocellular carcinoma (HCC) is a major cause of cancer death in the world. The aim of this study was to establish a new model to predict the prognosis of HCC.

MATERIALS AND METHODS

The mRNA, miRNA and lncRNA expression profiles of early (stage I-II) and late (stage III-IV) stage HCC patients were acquired from The Cancer Genome Atlas (TCGA) database. The differentially expressed mRNAs (DEmRNAs), miRNAs (DEmiRNAs) and lncRNAs (DElncRNAs) were identified between early and late stage HCC. Key molecules associated with the prognosis, and important immune cell types in HCC were identified. The nomogram based on incorporating age, gender, stage, and all important factors was constructed to predict the survival of HCC.

RESULTS

A total of 1516 DEmRNAs, 97 DEmiRNAs and 87 DElncRNAs were identified. A DElncRNA-DEmiRNA-DEmRNA regulatory network including 78 mRNAs, 50 miRNAs and 1 lncRNA was established. Among the regulatory network, 11 molecules were significantly correlated with the prognosis of HCC based on Lasso regression analysis. Then, Preadipocytes and 3 survival-associated DEmRNAs were identified as crucial biomarkers. Subsequently, a nomogram with a differentiation degree of 0.758, including 1 immune cell, 11 mRNAs and 3 miRNAs, was generated.

CONCLUSION

Our study constructed a model by incorporating clinical information, significant biomarkers and immune cells to predict the survival of HCC, which achieved a good performance.

摘要

背景

肝细胞癌(HCC)是全球癌症死亡的主要原因。本研究的目的是建立一种预测HCC预后的新模型。

材料与方法

从癌症基因组图谱(TCGA)数据库中获取早期(I-II期)和晚期(III-IV期)HCC患者的mRNA、miRNA和lncRNA表达谱。鉴定早期和晚期HCC之间差异表达的mRNA(DEmRNA)、miRNA(DEmiRNA)和lncRNA(DElncRNA)。确定与预后相关的关键分子以及HCC中的重要免疫细胞类型。构建包含年龄、性别、分期和所有重要因素的列线图以预测HCC的生存率。

结果

共鉴定出1516个DEmRNA、97个DEmiRNA和87个DElncRNA。建立了一个包含78个mRNA、50个miRNA和1个lncRNA的DElncRNA-DEmiRNA-DEmRNA调控网络。在调控网络中,基于套索回归分析,11个分子与HCC的预后显著相关。然后,前脂肪细胞和3个与生存相关的DEmRNA被确定为关键生物标志物。随后,生成了一个分化度为0.758的列线图,包括1种免疫细胞、11个mRNA和3个miRNA。

结论

我们的研究通过整合临床信息、重要生物标志物和免疫细胞构建了一个预测HCC生存率的模型,该模型具有良好的性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ae3/10281275/17891aab3c6f/IJGM-16-2519-g0001.jpg

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