AXL Downstream Targeting Unravels Synergistic Drug Combinations in Ovarian Carcinoma Cells

Anticancer Res. 2019 Jul;39(7):3803-3808. doi: 10.21873/anticanres.13529.

Abstract

Background: Platinum-based therapy represents the main pharmacological treatment for ovarian carcinoma. Since molecular targeting of receptor tyrosine kinases (RTK) affects factors that may modulate drug response, the aim of this study was to examine whether downstream targets of AXL RTK could be exploited to improve cell response to cisplatin.

Materials and methods: Inhibitors of p38 (SB203580) and of signal transducer and activator of transcription 3 (stattic) were employed in combination with cisplatin in ovarian carcinoma cell lines. Apoptosis assay and western blot analysis were performed to evaluate cell response after treatment.

Results: SB203580 produced a synergistic effect in combination with cisplatin in cisplatin-resistant IGROV-1/Pt1 cells. In addition, a favorable drug interaction was observed in A2780 cells when pre-incubated with cisplatin prior to stattic. The analysis of cell response after combined treatment showed down-regulation of the pro-apoptotic protein BCL2-associated agonist of cell death (BAD).

Conclusion: Our results support the notion that downstream targets of AXL in ovarian carcinoma cells can be exploited to increase cisplatin activity in ovarian carcinoma models.

Keywords: AXL; Ovarian carcinoma; cisplatin; p38 MAPK.

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Axl Receptor Tyrosine Kinase
  • Cell Line, Tumor
  • Cisplatin / pharmacology*
  • Drug Synergism
  • Female
  • Humans
  • Imidazoles / pharmacology*
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / metabolism*
  • Protein Kinase Inhibitors / pharmacology*
  • Proto-Oncogene Proteins / antagonists & inhibitors*
  • Proto-Oncogene Proteins / metabolism
  • Pyridines / pharmacology*
  • Receptor Protein-Tyrosine Kinases / antagonists & inhibitors*
  • Receptor Protein-Tyrosine Kinases / metabolism
  • STAT3 Transcription Factor
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors*

Substances

  • Antineoplastic Agents
  • Imidazoles
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins
  • Pyridines
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Receptor Protein-Tyrosine Kinases
  • p38 Mitogen-Activated Protein Kinases
  • SB 203580
  • Cisplatin
  • Axl Receptor Tyrosine Kinase
  • AXL protein, human