Prognostic and predictive role of a metabolic rate-limiting enzyme signature in hepatocellular carcinoma

被引:9
|
作者
Wang, Zhangding [1 ]
Fu, Yao [2 ]
Xia, Anliang [3 ]
Chen, Chen [4 ]
Qu, Jiamu [3 ]
Xu, Guifang [1 ]
Zou, Xiaoping [1 ]
Wang, Qiang [3 ]
Wang, Shouyu [3 ,4 ,5 ]
机构
[1] Nanjing Univ, Med Sch, Dept Gastroenterol, Affiliated Drum Tower Hosp, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Univ, Med Sch, Dept Pathol, Affiliated Drum Tower Hosp, Nanjing, Peoples R China
[3] Nanjing Univ, Med Sch, Dept Hepatobiliary Surg, Affiliated Drum Tower Hosp, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Univ, Jiangsu Key Lab Mol Med, Med Sch, Nanjing, Peoples R China
[5] Nanjing Univ, Ctr Publ Hlth Res, Med Sch, Nanjing, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
hepatocellular carcinoma; metabolism; prognosis; rate-limiting enzymes; signature; CANCER; RRM1; IDENTIFICATION; SURVIVAL; CELLS;
D O I
10.1111/cpr.13117
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objectives Abnormal expression of metabolic rate-limiting enzymes drives the occurrence and progression of hepatocellular carcinoma (HCC). This study aimed to elucidate the comprehensive model of metabolic rate-limiting enzymes associated with the prognosis of HCC. Materials and Methods HCC animal model and TCGA project were used to screen out differentially expressed metabolic rate-limiting enzyme. Cox regression, least absolute shrinkage and selection operation (LASSO) and experimentally verification were performed to identify metabolic rate-limiting enzyme signature. The area under the receiver operating characteristic curve (AUC) and prognostic nomogram were used to assess the efficacy of the signature in the three HCC cohorts (TCGA training cohort, internal cohort and an independent validation cohort). Results A classifier based on three rate-limiting enzymes (RRM1, UCK2 and G6PD) was conducted and serves as independent prognostic factor. This effect was further confirmed in an independent cohort, which indicated that the AUC at year 5 was 0.715 (95% CI: 0.653-0.777) for clinical risk score, whereas it was significantly increased to 0.852 (95% CI: 0.798-0.906) when combination of the clinical with signature risk score. Moreover, a comprehensive nomogram including the signature and clinicopathological aspects resulted in significantly predict the individual outcomes. Conclusions Our results highlighted the prognostic value of rate-limiting enzymes in HCC, which may be useful for accurate risk assessment in guiding clinical management and treatment decisions.
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页数:14
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