A Unique Metastasis Gene Signature Enables Prediction of Tumor Relapse in Early-Stage Hepatocellular Carcinoma Patients

  • Stephanie Roessler
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Hu-Liang Jia
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Anuradha Budhu
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Marshonna Forgues
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Qing-Hai Ye
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Ju-Seog Lee
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Snorri S. Thorgeirsson
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Zhongtang Sun
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Zhao-You Tang
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Lun-Xiu Qin
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China
  • Xin Wei Wang
    Authors' Affiliations: 1Laboratory of Human Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; 2Liver Cancer Institute & Zhongshan Hospital, Fudan University, Shanghai, China; 3Laboratory of Experimental Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; and 4National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences, Beijing, China

書誌事項

公開日
2010-12-14
DOI
  • 10.1158/0008-5472.can-10-2607
公開者
American Association for Cancer Research (AACR)

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<jats:title>Abstract</jats:title> <jats:p>Metastasis-related recurrence often occurs in hepatocellular carcinoma (HCC) patients who receive curative therapies. At present, it is challenging to identify patients with high risk of recurrence, which would warrant additional therapies. In this study, we sought to analyze a recently developed metastasis-related gene signature for its utility in predicting HCC survival, using 2 independent cohorts consisting of a total of 386 patients who received radical resection. Cohort 1 contained 247 predominantly HBV-positive cases analyzed with an Affymetrix platform, whereas cohort 2 contained 139 cases with mixed etiology analyzed with the NCI Oligo Set microarray platform. We employed a survival risk prediction algorithm with training, test, and independent cross-validation strategies and found that the gene signature is predictive of overall and disease-free survival. Importantly, risk was significantly predicted independently of clinical characteristics and microarray platform. In addition, survival prediction was successful in patients with early disease, such as small (&lt;5 cm in diameter) and solitary tumors, and the signature predicted particularly well for early recurrence risk (&lt;2 years), especially when combined with serum alpha fetoprotein or tumor staging. In conclusion, we have shown in 2 independent cohorts with mixed etiologies and ethnicity that the metastasis gene signature is a useful tool to predict HCC outcome, suggesting the general utility of this classifier. We recommend the use of this classifier as a molecular diagnostic test to assess the risk that an HCC patient will develop tumor relapse within 2 years after surgical resection, particularly for those with early-stage tumors and solitary presentation. Cancer Res; 70(24); 10202–12. ©2010 AACR.</jats:p>

収録刊行物

  • Cancer Research

    Cancer Research 70 (24), 10202-10212, 2010-12-14

    American Association for Cancer Research (AACR)

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