Metformin-induced caveolin-1 expression promotes T-DM1 drug efficacy in breast cancer cells

Sci Rep. 2018 Mar 2;8(1):3930. doi: 10.1038/s41598-018-22250-8.

Abstract

Trastuzumab emtansine (T-DM1) is an antibody drug conjugate (ADC) that was recently approved for the treatment of HER-2-positive metastatic breast cancer. The drug sensitivity of ADCs depends mainly on the internalization efficiency of the drug. Caveolin-1 was shown to promote T-DM1 internalization and enhance drug sensitivity. Whether caveolin-1 can be overexpressed to improve T-DM1 efficacy is interesting and has the potential for clinical application. In this study, diabetes drug metformin was investigated in terms of induction of caveolin-1 expression for increased efficacy of subsequent T-DM1 application. BT-474 cells were pretreated with metformin, followed by combined therapy with metformin and T-DM1. The T-DM1 internalization and drug efficacy were determined, and the protein expressions for signal transduction were also monitored. Caveolin-1 shRNA was applied to suppress endogenous caveolin-1 expression, and the ability of metformin to promote T-DM1 efficacy was investigated. Result showed that in BT-474 cells pretreated with metformin, cellular caveolin-1 overexpression was induced, which then promoted drug efficacy by enhancing T-DM1 internalization. As cellular caveolin-1 was suppressed by shRNA, the effect of metformin-enhanced T-DM1 cytotoxicity was decreased. This study demonstrated that metformin can be applied prior to T-DM1 treatment to improve the clinical efficacy of T-DM1 by enhancing caveolin-1-mediated endocytosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ado-Trastuzumab Emtansine
  • Antineoplastic Agents, Immunological / pharmacology*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Caveolin 1 / metabolism*
  • Drug Resistance, Neoplasm*
  • Drug Synergism
  • Endocytosis
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Immunoconjugates / pharmacology
  • Maytansine / analogs & derivatives*
  • Maytansine / pharmacology
  • Metformin / pharmacology*
  • Receptor, ErbB-2 / metabolism
  • Signal Transduction
  • Trastuzumab / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents, Immunological
  • CAV1 protein, human
  • Caveolin 1
  • Hypoglycemic Agents
  • Immunoconjugates
  • Maytansine
  • Metformin
  • Receptor, ErbB-2
  • Trastuzumab
  • Ado-Trastuzumab Emtansine