ADH1B型                        
                
                                
                        
                            小桶                        
                
                                
                        
                            肝细胞癌                        
                
                                
                        
                            肿瘤科                        
                
                                
                        
                            比例危险模型                        
                
                                
                        
                            恶性肿瘤                        
                
                                
                        
                            医学                        
                
                                
                        
                            内科学                        
                
                                
                        
                            外科肿瘤学                        
                
                                
                        
                            生存分析                        
                
                                
                        
                            生物信息学                        
                
                                
                        
                            生物                        
                
                                
                        
                            基因                        
                
                                
                        
                            基因表达                        
                
                                
                        
                            遗传学                        
                
                                
                        
                            转录组                        
                
                                
                        
                            生物化学                        
                
                                
                        
                            支链α-酮酸脱氢酶复合物                        
                
                                
                        
                            酶                        
                
                                
                        
                            脱氢酶                        
                
                        
                    
            作者
            
                Xiangye Liu,Tingting Li,Delong Kong,Hongjuan You,Fanyun Kong,Renxian Tang            
         
                    
            出处
            
                                    期刊:BMC Cancer
                                                         [BioMed Central]
                                                        日期:2020-12-01
                                                        卷期号:20 (1)
                                                        被引量:49
                                 
         
        
    
            
            标识
            
                                    DOI:10.1186/s12885-020-07689-1
                                    
                                
                                 
         
        
                
            摘要
            
            Abstract Background Hepatocellular carcinoma (HCC) is a malignancy with high incidence and mortality rates worldwide. Alcohol dehydrogenases (ADHs) are huge family of dehydrogenase enzymes and associated with the prognosis of various cancers. However, comprehensive analysis of prognostic implications related to ADHs in HCC is still lacking and largely unknown. Methods The expression profiles and corresponding clinical information of HCC were obtained from The Cancer Genome Atlas (TCGA). Wilcoxon signed-rank test was employed to evaluate the expression of ADHs. Cox regression and Kaplan-Meier analyses were used to investigate the association between clinicopathological characteristics and survival. GO (Gene Ontology) and KEGG (Kyoto Encyclopedia of Genes and Genomes) enrichment analyses were performed and visualized using R/BiocManager package. Results We found that the expression of ADH1A, ADH1B, ADH1C, ADH4, and ADH6 was significantly downregulated in HCC samples compared to normal liver samples. Our univariate and multivariate Cox regression analyses results showed that high expression of ADH1A, ADH1B, ADH1C, ADH4, and ADH6 was considered as an independent factor with an improved prognosis for the survival of HCC patients. Moreover, our Kaplan-Meier analysis results also revealed that high expression of AHD1A, ADH1B, ADH1C, ADH4, and ADH6 was significantly associated with good survival rate in HCC patients. In addition, GO, KEGG, and GSEA analyses unveiled several oncogenic signaling pathways were negatively associated high expression of ADHs in HCC. Conclusion In the present study, our results provide the potential prognostic biomarkers or molecular targets for the patients with HCC.
         
            
 
                 
                
                    
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