Prognostic and metabolic characteristics of a novel cuproptosis-related signature in patients with hepatocellular carcinoma

被引:0
|
作者
Qu, Xin [1 ]
Meng, Ling-cui [1 ]
Lu, Xi [2 ]
Chen, Xian [3 ]
Li, Yong [1 ]
Zhou, Rui [1 ]
Zhu, Yan-juan [4 ]
Luo, Yi-chang [1 ]
Huang, Jin-tao [5 ]
Shi, Xiao-liang [6 ]
Zhang, Hai-Bo [6 ,7 ]
机构
[1] Guangzhou Univ Chinese Med, Affiliated Hosp 2, Guangdong Prov Hosp Tradit Chinese Med, Dept Oncol, Guangzhou 510120, Peoples R China
[2] Guangzhou Univ Chinese Med, Affiliated Hosp 2, Guangdong Prov Hosp Tradit Chinese Med, Dept Ultrasound, Guangzhou 510120, Peoples R China
[3] Guangzhou Univ Tradit Chinese Med, Guangzhou Hosp Tradit Chinese Med, Guangzhou 510405, Peoples R China
[4] Guangzhou Univ Chinese Med, Clin Med Sch 2, Guangzhou 510120, Peoples R China
[5] Guangzhou Med Univ, Guangzhou Univ Tradit Chinese Med, Hosp Tradit Chinese Med, Guangzhou Hosp Tradit Chinese Med,Dept Oncol, Guangzhou 510130, Peoples R China
[6] Shanghai OrigiMed Co Ltd, Shanghai 201114, Peoples R China
[7] Guangdong Prov Hosp Tradit Chinese Med, Dept Oncol, 111 Dade Rd, Guangzhou 510120, Guangdong, Peoples R China
关键词
Cuproptosis; HCC; Metabolism; Prognosis; Treatment; PROGRESSION; SORAFENIB; APOPTOSIS; PATHWAY;
D O I
10.1016/j.heliyon.2023.e23686
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cuproptosis is a novel discovered mode of programmed cell death. To identify the molecular regulatory patterns related to cuproptosis, this study was designed for exploring the correlation between cuproptosis-related genes (CRGs) and the prognosis, metabolism, and treatment of hepatocellular carcinoma (HCC). Cancer Genome Atlas (TCGA) database was used to screen 363 HCC samples, which were categorized into 2 clusters based on the expression of CRGs. Survival analysis demonstrated that overall survival (OS) was better in Cluster 1 than Cluster 2 which might to be relevant to differences in metabolic based on functional analysis. With LASSO regression analysis and univariate COX regression, 8 prognosis-related genes were screened, a differently expressed genes (DEGs) were then constructed (HCC patients' DEGs)-based signature. The signature's stability was also validated in the 2 independent cohorts and test cohorts (GSE14520, HCC dataset in PCAWG). The 1-year, 3-year, and 5-year area under the curve (AUC) were 0.756, 0.706, and 0.722, respectively. The signature could also well predict the response to chemotherapy, targeted and transcatheter arterial chemoembolization (TACE) by providing a risk score. Moreover, the correlation was uncovered by the research between the metabolism and risk score. In conclusion, a unique cuproptosis-related signature that be capable of predicting patients' prognosis with HCC, and offered valuable insights into chemotherapy, TACE and targeted therapies for these patients has been developed.
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页数:13
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