Chemogenomic Study of Carboplatin in Saccharomyces cerevisiae: Inhibition of the NEDDylation Process Overcomes Cellular Resistance Mediated by HuR and Cullin Proteins

PLoS One. 2015 Dec 21;10(12):e0145377. doi: 10.1371/journal.pone.0145377. eCollection 2015.

Abstract

The use of carboplatin in cancer chemotherapy is limited by the emergence of drug resistance. To understand the molecular basis for this resistance, a chemogenomic screen was performed in 53 yeast mutants that had previously presented strong sensitivity to this widely used anticancer agent. Thirty-four mutants were responsive to carboplatin, and from these, 21 genes were selected for further studies because they have human homologues. Sixty percent of these yeast genes possessed human homologues which encoded proteins that interact with cullin scaffolds of ubiquitin ligases, or whose mRNA are under the regulation of Human antigen R (HuR) protein. Both HuR and cullin proteins are regulated through NEDDylation post-translational modification, and so our results indicate that inhibition of this process should sensitise resistant tumour cells to carboplatin. We showed that treatment of a tumour cell line with MLN4924, a NEDDylation inhibitor, overcame the resistance to carboplatin. Our data suggest that inhibition of NEDDylation may be a useful strategy to resensitise tumour cells in patients that have acquired carboplatin resistance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carboplatin / pharmacology*
  • Cell Line, Tumor / drug effects
  • Chromosomes, Human, Pair 1
  • Cullin Proteins / genetics*
  • Cullin Proteins / metabolism
  • Cyclopentanes / pharmacology
  • Drug Resistance, Fungal / drug effects
  • Drug Resistance, Fungal / physiology
  • Drug Resistance, Neoplasm / drug effects
  • Drug Resistance, Neoplasm / genetics*
  • ELAV-Like Protein 1 / genetics*
  • ELAV-Like Protein 1 / metabolism
  • Female
  • Gene Expression Profiling
  • Humans
  • Mutation
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / genetics
  • Pyrimidines / pharmacology
  • Saccharomyces cerevisiae / drug effects*
  • Saccharomyces cerevisiae / genetics*
  • Ubiquitin-Activating Enzymes / antagonists & inhibitors
  • Ubiquitin-Activating Enzymes / genetics
  • Ubiquitin-Activating Enzymes / metabolism

Substances

  • Cullin Proteins
  • Cyclopentanes
  • ELAV-Like Protein 1
  • ELAVL1 protein, human
  • Pyrimidines
  • Carboplatin
  • Ubiquitin-Activating Enzymes
  • NAE protein, human
  • pevonedistat

Grants and funding

This work was supported by GFS received grant by Fundação de Amparo à Pesquisa do Estado de São Paulo - grant number 2011/04173-1 to GFS, and by Fundação de Amparo à Pesquisa do Estado de São Paulo - grant numbers 2009/01303-1 and 2015/07749-2 to GM. DFC, MAL and VMF received no specific funding for this work.