ZBTB7A acts as a tumor suppressor through the transcriptional repression of glycolysis

Xue Song Liu, Jenna E. Haines, Elie K. Mehanna, Matthew D. Genet, Issam Ben-Sahra, John M. Asara, Brendan D. Manning, Zhi Min Yuan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

61 Scopus citations

Abstract

Elevated glycolysis is a common metabolic trait of cancer, but what drives such metabolic reprogramming remains incompletely clear. We report here a novel transcriptional repressor-mediated negative regulation of glycolysis. ZBTB7A, a member of the POK (POZ/BTB and Krüppel) transcription repressor family, directly binds to the promoter and represses the transcription of critical glycolytic genes, including GLUT3, PFKP, and PKM. Analysis of The Cancer Genome Atlas (TCGA) data sets reveals that the ZBTB7A locus is frequently deleted in many human tumors. Significantly, reduced ZBTB7A expression correlates with up-regulation of the glycolytic genes and poor survival in colon cancer patients. Remarkably, while ZBTB7A-deficient tumors progress exceedingly fast, they exhibit an unusually heightened sensitivity to glycolysis inhibition. Our study uncovers a novel tumor suppressor role of ZBTB7A in directly suppressing glycolysis.

Original languageEnglish (US)
Pages (from-to)1917-1928
Number of pages12
JournalGenes and Development
Volume28
Issue number17
DOIs
StatePublished - Sep 1 2014

Keywords

  • GLUT3
  • Glycolysis
  • PFKP
  • PKM
  • Tumor suppressor
  • ZBTB7A

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology

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