Ovarian cancer cells cisplatin sensitization agents selected by mass cytometry target ABCC2 inhibition

Future Med Chem. 2018 Jun 1;10(11):1349-1360. doi: 10.4155/fmc-2017-0308. Epub 2018 May 31.

Abstract

Aim: Cisplatin resistance in ovarian cancer remains a complex problem as tumors frequently develop resistance against drugs, a mechanism sometimes mediated by ATP-Binding Cassette transporters. Our goal was to find compounds restricting their inhibition capacity to the cisplatin efflux mediated by ABCC2 pump, among previously identified inhibitors, derived from the 2- indolylmethylenebenzofuranones. Methodology & results: An original method setup allows direct quantitation of platinum by employing cyTOF mass cytometry. Among tested derivatives, some led to a full platinum accumulation and efficiently resensitized cisplatin-resistant A2780 cells to cisplatin while preserving most of the calcein efflux activity.

Conclusion: CyTOF is therefore a powerful and promising method to quantify cisplatin accumulation that may be used in the clinical setting to improve and personalize cancer treatment.

Keywords: ABCC2 aurones; cisplatin resistance; cyTOF inhibitors; mass cytometry; multidrug resistance; ovarian cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Benzofurans / chemical synthesis
  • Benzofurans / pharmacology*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Cisplatin / pharmacology*
  • Drug Resistance, Neoplasm / drug effects*
  • Female
  • Fluoresceins / metabolism
  • Humans
  • Multidrug Resistance-Associated Protein 2
  • Multidrug Resistance-Associated Proteins / antagonists & inhibitors*
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / pathology*

Substances

  • ABCC2 protein, human
  • Antineoplastic Agents
  • Benzofurans
  • Fluoresceins
  • Multidrug Resistance-Associated Protein 2
  • Multidrug Resistance-Associated Proteins
  • Cisplatin
  • fluorexon