Integrin-β4 is a novel transcriptional target of TAp73

Cell Cycle. 2018;17(5):589-594. doi: 10.1080/15384101.2017.1403684. Epub 2018 Feb 8.

Abstract

As a member of p53 family, p73 has attracted intense investigations due to its structural and functional similarities to p53. Among more than ten p73 variants, the transactivation (TA) domain-containing isoform TAp73 is the one that imitates the p53's behavior most. TAp73 induces apoptosis and cell cycle arrest, which endows it the capacity of tumour suppression. Also, it can exert diverse biological influences on cells through activating a complex and context dependent transcriptional programme. The transcriptional activities further broaden its roles in more intricate biological processes. In this article, we report that p73 is a positive regulator of a cell adhesion related gene named integrin β4 (ITGB4). This finding may have implications for the dissection of the biological mechanisms underlining p73 functions.

Keywords: Integrins; adhesion and migration; cancer cells; cell interaction; oncogenes and tumor suppressors; oncosupression; p53 family; p73; transcription factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Checkpoints
  • Cell Line, Tumor
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • HEK293 Cells
  • Humans
  • Integrin beta4 / genetics
  • Integrin beta4 / metabolism*
  • Promoter Regions, Genetic
  • Protein Binding
  • Transcription, Genetic*
  • Transfection
  • Tumor Protein p73 / genetics
  • Tumor Protein p73 / metabolism*

Substances

  • Cyclin-Dependent Kinase Inhibitor p21
  • Integrin beta4
  • Tumor Protein p73