Plasminogen activator inhibitor-1 as regulator of tumor-initiating cell properties in head and neck cancers

Head Neck. 2016 Apr:38 Suppl 1:E895-904. doi: 10.1002/hed.24124. Epub 2015 Jul 16.

Abstract

Background: The existence of tumor-initiating cells (TICs) has been described in head and neck cancers. Plasminogen activator inhibitor-1 (PAI-1) has been demonstrated to act as a prognostic factor in head and neck cancers.

Methods: Tiplaxtinin (PAI-039), a specific inhibitor of PAI-1, and PAI-1-specific siRNA were used to examine the role of PAI-1 in the self-renewal property of head and neck cancer-TICs by tumorsphere formation. Western blot, real-time polymerase chain reaction, and luciferase-based reporter assay were used to study the effect of PAI-039 in the sex-determining region Y-box 2 (Sox2) expression.

Results: PAI-039 suppressed the self-renewal capability of head and neck cancer-TICs derived from head and neck cancer cell lines through the inhibition of Sox2 expression. PAI-039 decreased the activity of the core promoter and the enhancer of the Sox2 gene in head and neck cancer-TICs. Knockdown of PAI-1 expression also inhibited self-renewal and radioresistance properties of head and neck cancer-TICs.

Conclusion: The inhibition of PAI-1 by PAI-039 or siRNA could suppress head and neck cancer-TICs within head and neck cancer cell lines through the downregulation of Sox2. © 2015 Wiley Periodicals, Inc. Head Neck 38: E895-E904, 2016.

Keywords: Sox2; head and neck cancer; plasminogen activator inhibitor-1 (PAI-1); tiplaxtinin (PAI-039); tumor-initiating cells.

MeSH terms

  • Cell Line, Tumor
  • Enhancer Elements, Genetic
  • Gene Knockdown Techniques
  • Head and Neck Neoplasms / metabolism
  • Head and Neck Neoplasms / pathology*
  • Humans
  • Indoleacetic Acids / pharmacology
  • Neoplastic Stem Cells / metabolism*
  • Plasminogen Activator Inhibitor 1 / metabolism*
  • Promoter Regions, Genetic
  • RNA, Small Interfering / genetics
  • Real-Time Polymerase Chain Reaction
  • SOXB1 Transcription Factors / metabolism*

Substances

  • Indoleacetic Acids
  • Plasminogen Activator Inhibitor 1
  • RNA, Small Interfering
  • SERPINE1 protein, human
  • SOX2 protein, human
  • SOXB1 Transcription Factors
  • tiplaxtinin