4.6 Article

Identification and validation of a prognostic four-genes signature for hepatocellular carcinoma: integrated ceRNA network analysis

期刊

HEPATOLOGY INTERNATIONAL
卷 13, 期 5, 页码 618-630

出版社

SPRINGER
DOI: 10.1007/s12072-019-09962-3

关键词

Hepatocellular carcinoma; Overall survival; Competing endogenous RNA; Least absolute shrinkage and selection operator; Global transcriptome

资金

  1. National Natural Science Foundation of China [81572407, 81602112, 81672405]
  2. Key project of Natural Science Foundation of Guangdong Province, China [4210016041]
  3. Science and Technology Program of Guangdong Province, China [2015A030313096, 2016A030313184]
  4. Natural Science Foundation of Guangzhou, China [4250016043]
  5. Key Laboratory of Malignant Tumor Molecular Mechanism and Translational Medicine of Guangzhou Bureau of Science and Information Technology [[2013] 163]
  6. Key Laboratory of Malignant Tumor Gene Regulation and Target Therapy of Guangdong Higher Education Institutes [KLB09001]

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Background Hepatocellular carcinoma (HCC) is one of the most aggressive malignant tumors, with a poor long-term prognosis worldwide. The functional deregulations of global transcriptome were associated with the genesis and development of HCC, but lacks systematic research and validation. Methods A total of 519 postoperative HCC patients were included. We built an interactive and visual competing endogenous RNA network. The prognostic signature was established with the least absolute shrinkage and selection operator algorithm. Multivariate Cox regression analysis was used to screen for independent prognostic factors for HCC overall survival. Results In the training set, we identified a four-gene signature (PBK, CBX2, CLSPN, and CPEB3) and effectively predicted the overall survival. The survival times of patients in the high-score group were worse than those in the low-score group (p = 0.0004), and death was also more likely in the high-score group (HR 2.444, p < 0.001). The results were validated in internal validation set (p = 0.0057) and two external validation cohorts (HR 2.467 and 2.6). The signature (AUCs of 1, 2, 3 years were 0.716, 0.726, 0.714, respectively) showed high prognostic accuracy in the complete TCGA cohort. Conclusions In conclusion, we successfully built a more extensive ceRNA network for HCC and then identified a four-gene-based signature, enabling prediction of the overall survival of patients with HCC.

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