CDC20 maintains tumor initiating cells

Oncotarget. 2015 May 30;6(15):13241-54. doi: 10.18632/oncotarget.3676.

Abstract

Glioblastoma is the most prevalent and lethal primary intrinsic brain tumor. Glioblastoma displays hierarchical arrangement with a population of self-renewing and tumorigenic glioma tumor initiating cells (TICs), or cancer stem cells. While non-neoplastic neural stem cells are generally quiescent, glioblastoma TICs are often proliferative with mitotic control offering a potential point of fragility. Here, we interrogate the role of cell-division cycle protein 20 (CDC20), an essential activator of anaphase-promoting complex (APC) E3 ubiquitination ligase, in the maintenance of TICs. By chromatin analysis and immunoblotting, CDC20 was preferentially expressed in TICs relative to matched non-TICs. Targeting CDC20 expression by RNA interference attenuated TIC proliferation, self-renewal and in vivo tumor growth. CDC20 disruption mediated its effects through induction of apoptosis and inhibition of cell cycle progression. CDC20 maintains TICs through degradation of p21CIP1/WAF1, a critical negative regulator of TICs. Inhibiting CDC20 stabilized p21CIP1/WAF1, resulting in repression of several genes critical to tumor growth and survival, including CDC25C, c-Myc and Survivin. Transcriptional control of CDC20 is mediated by FOXM1, a central transcription factor in TICs. These results suggest CDC20 is a critical regulator of TIC proliferation and survival, linking two key TIC nodes-FOXM1 and p21CIP1/WAF1-elucidating a potential point for therapeutic intervention.

Keywords: CDC20; cancer stem cell; glioblastoma; glioma; tumor initiating cell.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / pathology
  • Cdc20 Proteins / metabolism*
  • Cell Proliferation / physiology
  • Cell Survival / physiology
  • Chromatin Immunoprecipitation
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • Forkhead Box Protein M1
  • Forkhead Transcription Factors / metabolism
  • Glioblastoma / metabolism*
  • Glioblastoma / pathology
  • Heterografts
  • Humans
  • Mice
  • Mice, Inbred NOD
  • Neoplastic Stem Cells / metabolism*
  • Tumor Cells, Cultured

Substances

  • CDKN1A protein, human
  • Cdc20 Proteins
  • Cyclin-Dependent Kinase Inhibitor p21
  • FOXM1 protein, human
  • Forkhead Box Protein M1
  • Forkhead Transcription Factors
  • CDC20 protein, human