Combining a GSI and BCL-2 inhibitor to overcome melanoma's resistance to current treatments

Oncotarget. 2016 Dec 20;7(51):84594-84607. doi: 10.18632/oncotarget.13141.

Abstract

Major limitations of current melanoma treatments are for instances of relapse and the lack of therapeutic options for BRAF wild-type patients who do not respond to immunotherapy. Many studies therefore focus on killing resistant subpopulations, such as Melanoma Initiating Cells (MICs) to prevent relapse. Here we examined whether combining a GSI (γ-Secretase Inhibitor) with ABT-737 (a small molecule BCL-2/BCL-XL/BCL-W inhibitor) can kill both the non-MICs (bulk of melanoma) and MICs. To address the limitations of melanoma therapies, we included multiple tumor samples of patients relapsed from current treatments, with a diverse genetic background (with or without the common BRAF, NRAS or NF1 mutations) in these studies. Excitingly, the combination treatment reduced cell viability and induced apoptosis of the non-MICs; disrupted primary spheres, decreased the ALDH+ cells, and inhibited the self-renewability of the MICs in multiple melanoma cell lines and relapsed patient samples. Using a low-cell-number mouse xenograft model, we demonstrated that the combination significantly reduced the tumor initiating ability of MIC-enriched cultures from relapsed patient samples. Mechanistic studies also indicate that cell death is NOXA-dependent. In summary, this combination may be a promising strategy to address treatment relapse and for triple wild-type patients who do not respond to immunotherapy.

Keywords: ABT-737; BRAF-WT melanoma; GSI-I; melanoma initiating cells; melanoma stem cells.

MeSH terms

  • Amyloid Precursor Protein Secretases / antagonists & inhibitors
  • Animals
  • Apoptosis / drug effects
  • Biphenyl Compounds / pharmacology*
  • Cell Line, Tumor
  • Cell Self Renewal / drug effects
  • Drug Resistance, Neoplasm
  • Drug Synergism
  • Drug Therapy, Combination*
  • Female
  • GTP Phosphohydrolases / genetics
  • Humans
  • Melanoma / drug therapy*
  • Melanoma / genetics
  • Melanoma / pathology
  • Membrane Proteins / genetics
  • Mice
  • Mice, Nude
  • Mutation / genetics
  • Neoplasm Recurrence, Local
  • Neoplastic Stem Cells / drug effects*
  • Neoplastic Stem Cells / physiology
  • Neurofibromin 1 / genetics
  • Nitrophenols / pharmacology*
  • Oligopeptides / pharmacology*
  • Piperazines / pharmacology
  • Proto-Oncogene Proteins B-raf / genetics
  • Proto-Oncogene Proteins c-bcl-2 / antagonists & inhibitors
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Sulfonamides / pharmacology*
  • Xenograft Model Antitumor Assays

Substances

  • ABT-737
  • Biphenyl Compounds
  • Membrane Proteins
  • Neurofibromin 1
  • Nitrophenols
  • Oligopeptides
  • PMAIP1 protein, human
  • Piperazines
  • Proto-Oncogene Proteins c-bcl-2
  • Sulfonamides
  • benzyloxycarbonyl-leucyl-leucyl-norleucinal
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • Amyloid Precursor Protein Secretases
  • GTP Phosphohydrolases
  • NRAS protein, human