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几种自噬相关基因与肝癌预后价值的相关性研究:基于 TCGA、GEPIA 和 HPA 数据库的研究。

The association between several autophagy-related genes and their prognostic values in hepatocellular carcinoma: a study on the foundation of TCGA, GEPIA and HPA databases.

机构信息

College of Biological Sciences and Biotechnology, Beijing Forestry University, 100083, Beijing, China.

Department of Clinical Laboratory, Beijing Ditan Hospital, Capital Medical University, 100015, Beijing, China.

出版信息

Mol Biol Rep. 2022 Nov;49(11):10269-10277. doi: 10.1007/s11033-022-07426-w. Epub 2022 Sep 12.

Abstract

BACKGROUND

The purpose of this study was to investigate the relationship between the expression of autophagy-related genes and prognosis in hepatocellular carcinoma (HCC).

METHODS AND RESULTS

We selected three autophagy-related genes (ATG3, ATG7, and ATG9A) from gene expression data of liver cancer patients in The Cancer Genome Atlas (TCGA) database by Kaplan-Meier survival analysis, univariate and multivariate Cox regression analysis, and Gene Set Enrichment Analysis (GSEA). Human Protein Atlas (HPA) and Gene Expression Profiling Interactive Analysis (GEPIA) databases were applied to testify the credibility of our results. The expression levels of ATG3, ATG7, and ATG9A were verified by real-time quantitative PCR (RT-qPCR) in normal liver cells (L02) and three HCC cell lines (HepG2, Hep3b, and Li-7). Data analysis results from TCGA showed high ATG3, ATG7, ATG9A expression in HCC tumor tissues. Kaplan-Meier survival analysis showed that the survival rate of the high expression group of ATG3, ATG7, and ATG9A was all significantly lower than the low expression group. GSEA analysis showed that many signaling pathways (such as the regulation of autophagy, glycine serine and threonine metabolism, pathways in cancer, mitogen-activated protein kinase (MAPK) signaling pathway, mammalian target of rapamycin (mTOR) signaling pathway, as well as P53 signaling pathway) were differentially enriched in HCCs with ATG3, ATG7, and ATG9A expression. GEPIA and RT-qPCR also identified that the mRNA expression level of ATG3, ATG7, and ATG9A in normal liver cells were significantly lower than in HCC cells. High protein expression of ATG3, ATG7, and ATG9A was displayed in HCCs from the HPA database.

CONCLUSIONS

The ATG3, ATG7, ATG9A might be utilized as prognostic biomarkers for liver cancer.

摘要

背景

本研究旨在探讨自噬相关基因的表达与肝细胞癌(HCC)预后之间的关系。

方法和结果

我们通过 Kaplan-Meier 生存分析、单因素和多因素 Cox 回归分析以及基因集富集分析(GSEA),从癌症基因组图谱(TCGA)数据库中肝癌患者的基因表达数据中选择了三个自噬相关基因(ATG3、ATG7 和 ATG9A)。人类蛋白质图谱(HPA)和基因表达谱交互式分析(GEPIA)数据库被用于验证我们结果的可信度。通过实时定量 PCR(RT-qPCR)在正常肝细胞(L02)和三个 HCC 细胞系(HepG2、Hep3b 和 Li-7)中验证了 ATG3、ATG7 和 ATG9A 的表达水平。TCGA 的数据分析结果显示 HCC 肿瘤组织中 ATG3、ATG7 和 ATG9A 的表达水平较高。Kaplan-Meier 生存分析表明,ATG3、ATG7 和 ATG9A 高表达组的生存率均明显低于低表达组。GSEA 分析表明,在 ATG3、ATG7 和 ATG9A 表达的 HCC 中,许多信号通路(如自噬的调控、甘氨酸丝氨酸和苏氨酸代谢、癌症途径、丝裂原活化蛋白激酶(MAPK)信号通路、哺乳动物雷帕霉素(mTOR)信号通路以及 P53 信号通路)存在差异富集。GEPIA 和 RT-qPCR 还确定了 ATG3、ATG7 和 ATG9A 在正常肝细胞中的 mRNA 表达水平明显低于 HCC 细胞。HPA 数据库显示 HCC 中存在 ATG3、ATG7 和 ATG9A 的高蛋白质表达。

结论

ATG3、ATG7、ATG9A 可能作为肝癌的预后生物标志物。

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