Prognostic implications of alcohol dehydrogenases in hepatocellular carcinoma

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 支链α-酮酸脱氢酶复合物 生物化学 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]
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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