[YARS1在肝细胞癌中的表达及其预后影响]。

Q3 Medicine
L H Hu, J Pan, H Cheng, T T Yao, J D Qian, L J Cao, M Chai, J Y Chai, G Q Wang, Y Wang
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引用次数: 0

摘要

目的:探讨基于蛋白的tRNA合成酶(YARS1)亚型YARS1在肝细胞癌中的表达及其对基因集富集分析的预后影响。方法:通过挖掘Cancer Genome Atlas数据库,比较并记录肝细胞癌患者肿瘤组织样本(374例)和癌旁组织样本(50例)中YARS1基因的表达情况。根据这些数据将肝细胞癌患者分为高表达组和低表达组。采用Logistic回归分析YARS1与肝细胞癌患者临床病理特征的关系。采用Kaplan-Meier法和log-rank检验分析YARS1表达对肝癌患者预后的影响。采用单因素和多因素Cox回归分析YARS1基因对肝细胞癌的预后价值。通过基因集富集分析,探讨YARS1在肝细胞癌发生发展中的相关基因通路。结果:YARS1基因在肝细胞癌组织中的表达高于正常组织(PYARS1与患者的分级相关(p < 0.05))。kapan - meier法和对数秩检验结果显示,YARS1基因高表达患者的生存率低于YARS1基因低表达患者(PYARS1被作为肝细胞癌的独立预后因素[危险比=1.10,95%可信区间(1.050-1.156)],PYARS1参与嘧啶代谢、嘌呤代谢、氨酰基tRNA生物合成、脂肪酸代谢、ppar信号转导通路、卵细胞减数分裂、氨基酸和核苷酸糖代谢、RNA降解、补体途径、缬氨酸和异亮氨酸降解、剪接体等途径。结论:YARS1的高表达与肝细胞癌的进展和预后有关。因此,该基因有望成为一种新的生物标志物和肝癌生物治疗的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Expression of YARS1 in hepatocellular carcinoma and its prognostic effect].

Objective: To explore the expression of YARS1, the subform of protein-based tRNA synthase (YARS1), and its prognostic effect on the analysis of gene set enrichment in hepatocellular carcinoma Methods: The expressional condition of the YARS1 gene in tumor tissue samples (374 cases) and adjacent tissue samples (50 cases) of hepatocellular carcinoma patients was compared and recorded by mining the Cancer Genome Atlas database. Hepatocellular carcinoma patients were divided into high expression and low expression groups according to this data. Logistic regression was used to analyze the relationship between YARS1 and the clinical pathological characteristics of hepatocellular carcinoma patients. The effect of YARS1 expression on the prognosis of hepatocellular carcinoma patients was analyzed by the Kaplan-Meier method and log-rank test. The prognostic value of the YARS1 gene for hepatocellular carcinoma was analyzed by univariate and multivariate Cox regression. Gene set enrichment analysis was used to evaluate the gene pathways related to YARS1 in the occurrence and development of hepatocellular carcinoma. Results: The expression of the YARS1 gene was higher in hepatocellular carcinoma tissue than in normal tissue (P<0.001). The expression level of YARS1 was correlated with the grade of patients (P<0.05), but not with age, gender, TNM stage, and others (P>0.05). The results of Kaplan-Meier method and log-rank test showed that the survival rate was lower in patients with high YARS1 gene expression than that of patients with low YARS1 gene expression (P<0.001). The results of multivariate Cox regression analysis showed that YARS1 was used as an independent prognostic factor for hepatocellular carcinoma [hazard ratio=1.10, 95% confidence interval (1.050-1.156), P<0.001]. The results of gene set enrichment analysis showed that YARS1 was involved in pyrimidine metabolism, purine metabolism, aminoacyl tRNA biosynthesis, fatty acid metabolism, ppar signal transduction pathway, oocyte meiosis, amino acid and nucleotide sugar metabolism, RNA degradation, complement pathway, valine and isoleucine degradation, spliceosome, and other pathways. Conclusion: The high expression of YARS1 is associated with the progression and prognosis of hepatocellular carcinoma. Therefore, this gene is expected to become a novel biomarker and a sort of target for biological therapy in hepatocellular carcinoma.

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来源期刊
中华肝脏病杂志
中华肝脏病杂志 Medicine-Medicine (all)
CiteScore
1.20
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0.00%
发文量
7574
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