Modularity of the metabolic gene network as a prognostic biomarker for hepatocellular carcinoma

ORAL

Abstract

Abnormal metabolism is an emerging hallmark of cancer. Cancer cells utilize both aerobic glycolysis and oxidative phosphorylation for energy production and biomass synthesis. In this work, we analyzed the expression patterns of metabolism genes in terms of modularity for 371 hepatocellular carcinoma (HCC) samples from the Cancer Genome Atlas (TCGA). We found that higher modularity significantly correlated with glycolytic phenotype, later tumor stages, higher metastatic potential, and cancer recurrence, all of which contributed to poorer prognosis. Furthermore, we developed metrics to calculate individual modularity, which was shown to be predictive of cancer recurrence and patients’ survival and therefore may serve as a prognostic biomarker. Our overall conclusion is that more aggressive HCC tumors, as judged by decreased host survival probability, had more modular expression patterns of metabolic genes.

*Fengdan Ye and Michael Deem are supported by NSF grant PHY-1427654. Dongya Jia is supported by PHY-1427654, DMS-1361411 and PHY-1605817. Herbert Levine is supported by PHY-1427654, DMS-1361411, PHY-1605817 and CPRIT grants R1111. Mingyang Lu is supported by the National Cancer Institute of the National Institutes of Health grant P30CA034196.

Presenters

  • Fengdan Ye

    • Rice University

Authors

  • Fengdan Ye

    • Rice University
  • Dongya Jia

    • Rice University
  • Mingyang Lu

    • The Jackson Laboratory
  • Herbert Levine

    • Department of Bioengineering, Rice University, Houston, Texas, Center for Theoretical Biological Physics, Rice University, Houston, Texas
    • Rice University
  • Michael W Deem

    • Rice University