Development and validation of robust metabolism-related gene signature in the prognostic prediction of hepatocellular carcinoma

被引:2
|
作者
Pan, Yangxun [1 ]
Zhang, Deyao [1 ]
Chen, Yuheng [2 ,3 ]
Li, Huake [4 ]
Wang, Jiongliang [1 ]
Yuan, Ze [1 ]
Sun, Liyang [1 ]
Zhou, Zhongguo [1 ]
Chen, Minshan [1 ,5 ]
Zhang, Yaojun [1 ,5 ]
Hu, Dandan [1 ,5 ]
机构
[1] Sun Yat sen Univ, Canc Ctr, Dept Liver Surg, State Key Lab Oncol South China, Guangzhou, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Hepatobiliary Ctr, Nanjing, Peoples R China
[3] Chinese Acad Med Sci, Res Unit Liver Transplantat & Transplant Immunol, Nanjing, Peoples R China
[4] Changning Cty Peoples Hosp, Dept Oncol, Baoshan, Peoples R China
[5] Sun Yat Sen Univ, Canc Ctr, Dept Liver Surg, 651 Dongfeng East Rd, Guangzhou 510060, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatocellular carcnioma; metabolic studies; nomogram; prognosis; CELLS; IMPACT; TUMORS; LIVER;
D O I
10.1111/jcmm.17718
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hepatocellular carcinoma (HCC) is one of the most common malignant tumours worldwide. Given metabolic reprogramming in tumours was a crucial hallmark, several studies have demonstrated its value in the diagnostics and surveillance of malignant tumours. The present study aimed to identify a cluster of metabolism-related genes to construct a prediction model for the prognosis of HCC. Multiple cohorts of HCC cases (466 cases) from public datasets were included in the present analysis. (GEO cohort) After identifying a list of metabolism-related genes associated with prognosis, a risk score based on metabolism-related genes was formulated via the LASSO-Cox and LASSO-pcvl algorithms. According to the risk score, patients were stratified into low- and high-risk groups, and further analysis and validation were accordingly conducted. The results revealed that high-risk patients had a significantly worse 5-year overall survival (OS) than low-risk patients in the GEO cohort. (30.0% vs. 57.8%; hazard ratio [HR], 0.411; 95% confidence interval [95% CI], 0.302-0.651; p < 0.001) This observation was confirmed in the external TCGA-LIHC cohort. (34.5% vs. 54.4%; HR 0.452; 95% CI, 0.299-0.681; p < 0.001) To promote the predictive ability of the model, risk score, age, gender and tumour stage were integrated into a nomogram. According to the results of receiver operating characteristic curves and decision curves analysis, the nomogram score possessed a superior predictive ability than conventional factors, which indicate that the risk score combined with clinicopathological features was able to achieve a robust prediction for OS and improve the individualized clinical decision making of HCC patients. In conclusion, the metabolic genes related to OS were identified and developed a metabolism-based predictive model for HCC. Through a series of bioinformatics and statistical analyses, the predictive ability of the model was approved.
引用
收藏
页码:1006 / 1020
页数:15
相关论文
共 50 条
  • [1] Development and Validation of a Propionate Metabolism-Related Gene Signature for Prognostic Prediction of Hepatocellular Carcinoma
    Xiao, Jincheng
    Wang, Jing
    Zhou, Chaoqun
    Luo, Junpeng
    JOURNAL OF HEPATOCELLULAR CARCINOMA, 2023, 10 : 1673 - 1687
  • [2] Development and validation of metabolism-related gene signature in prognostic prediction of gastric cancer
    Luo, Tianqi
    Li, Yuanfang
    Nie, Runcong
    Liang, Chengcai
    Liu, Zekun
    Xue, Zhicheng
    Chen, Guoming
    Jiang, Kaiming
    Liu, Ze-Xian
    Lin, Huan
    Li, Cong
    Chen, Yingbo
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2020, 18 : 3217 - 3229
  • [3] Establishment and validation of a cholesterol metabolism-related prognostic signature for hepatocellular carcinoma
    Tang, Linsong
    Wei, Rongli
    Chen, Ronggao
    Fan, Guanghan
    Zhou, Junbin
    Qi, Zhetuo
    Wang, Kai
    Wei, Qiang
    Wei, Xuyong
    Xu, Xiao
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2022, 20 : 4402 - 4414
  • [4] Establishment and validation of a cholesterol metabolism-related prognostic signature for hepatocellular carcinoma
    Tang, Linsong
    Wei, Rongli
    Chen, Ronggao
    Fan, Guanghan
    Zhou, Junbin
    Qi, Zhetuo
    Wang, Kai
    Wei, Qiang
    Wei, Xuyong
    Xu, Xiao
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2022, 20 : 4402 - 4414
  • [5] Establishment and validation of a cholesterol metabolism-related prognostic signature for hepatocellular carcinoma
    Tang, Linsong
    Wei, Rongli
    Chen, Ronggao
    Fan, Guanghan
    Zhou, Junbin
    Qi, Zhetuo
    Wang, Kai
    Wei, Qiang
    Wei, Xuyong
    Xu, Xiao
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2022, 20 : 4402 - 4414
  • [6] Prognostic Implication of a Novel Metabolism-Related Gene Signature in Hepatocellular Carcinoma
    Yuan, Chaoyan
    Yuan, Mengqin
    Chen, Mingqian
    Ouyang, Jinhua
    Tan, Wei
    Dai, Fangfang
    Yang, Dongyong
    Liu, Shiyi
    Zheng, Yajing
    Zhou, Chenliang
    Cheng, Yanxiang
    FRONTIERS IN ONCOLOGY, 2021, 11
  • [7] Identification of fatty acids synthesis and metabolism-related gene signature and prediction of prognostic model in hepatocellular carcinoma
    Ai Zhengdong
    Xing Xiaoying
    Fu Shuhui
    Liang Rui
    Tang Zehui
    Song Guanbin
    Yang Li
    Tang Xi
    Liu Wanqian
    Cancer Cell International, 24
  • [8] Identification of fatty acids synthesis and metabolism-related gene signature and prediction of prognostic model in hepatocellular carcinoma
    Ai, Zhengdong
    Xing, Xiaoying
    Fu, Shuhui
    Liang, Rui
    Tang, Zehui
    Song, Guanbin
    Yang, Li
    Xi, Tang
    Liu, Wanqian
    CANCER CELL INTERNATIONAL, 2024, 24 (01)
  • [9] A novel metabolism-related gene signature in patients with hepatocellular carcinoma
    Ru, Bin
    Hu, Jiaqi
    Zhang, Nannan
    Wan, Quan
    PEERJ, 2023, 11
  • [10] Development and Verification of a Combined Immune- and Metabolism-Related Prognostic Signature for Hepatocellular Carcinoma
    Guo, Yuanyuan
    Yang, Jing
    Gao, Hua
    Tian, Xin
    Zhang, Xiaojian
    Kan, Quancheng
    FRONTIERS IN IMMUNOLOGY, 2022, 13