Integrin β1-Mediated Cell⁻Cell Adhesion Augments Metformin-Induced Anoikis

Int J Mol Sci. 2019 Mar 7;20(5):1161. doi: 10.3390/ijms20051161.

Abstract

Cell⁻cell adhesion plays an important role in regulation of cell proliferation, migration, survival, and drug sensitivity. Metformin, a first line drug for type 2 diabetes, has been shown to possess anti-cancer activities. However, whether cell⁻cell adhesion affects metformin anti-cancer activity is unknown. In this study, Microscopic and FACS analyses showed that metformin induced cancer cell⁻cell adhesion exemplified by cell aggregation and anoikis under glucose restriction. Furthermore, western blot and QPCR analyses revealed that metformin dramatically upregulated integrin β1 expression. Silencing of integrin β1 significantly disrupted cell aggregation and reduced anoikis induced by metformin. Moreover, we showed that p53 family member ΔNp63α transcriptionally suppressed integrin β1 expression and is responsible for metformin-mediated upregulation of integrin β1. In summary, this study reveals a novel mechanism for metformin anticancer activity and demonstrates that cell⁻cell adhesion mediated by integrin β1 plays a critical role in metformin-induced anoikis.

Keywords: anoikis; cell adhesion; integrin β1; metformin; ΔNp63α.

MeSH terms

  • Anoikis
  • Cell Adhesion / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Gene Expression Regulation, Neoplastic / drug effects
  • Gene Silencing
  • Glucose / pharmacology*
  • HEK293 Cells
  • Humans
  • Integrin beta1 / genetics*
  • Integrin beta1 / metabolism*
  • Metformin / pharmacology*
  • Neoplasms / drug therapy
  • Neoplasms / genetics
  • Neoplasms / metabolism*
  • Transcription Factors / metabolism
  • Tumor Suppressor Proteins / metabolism
  • Up-Regulation

Substances

  • Integrin beta1
  • TP63 protein, human
  • Transcription Factors
  • Tumor Suppressor Proteins
  • Metformin
  • Glucose