Use of dual mTOR inhibitor MLN0128 against everolimus-resistant breast cancer

Breast Cancer Res Treat. 2018 Aug;170(3):499-506. doi: 10.1007/s10549-018-4779-x. Epub 2018 Apr 5.

Abstract

Purpose: HR+/HER2- aromatase inhibitor-resistant metastatic breast cancer can be treated with everolimus and a second AI until the cancer recurs. Targeting these everolimus-resistant patients with the latest standard of care, CDK4/6 inhibitors, has not been clearly addressed. Understanding the signaling transduction pathways, which everolimus resistance activates, will elucidate the mechanisms and offer treatment strategies of everolimus resistance.

Methods: To mimic the clinical setting, letrozole-resistant cells were used to generate an everolimus-resistant model (RAD-R). Reverse phase protein array (RPPA) was performed to reveal changes in the signaling transduction pathways, and expression levels of key proteins were analyzed. Inhibitors targeting the major signaling pathways, a CDK4/6 inhibitor palbociclib and a mTORC1/2 inhibitor (MLN0128), were evaluated to establish resistance mechanisms of RAD-R.

Results: RPPA results from RAD-R indicated changes to significant regulatory pathways and upregulation of p-AKT expression level associating with everolimus resistance. MLN0128, that inhibits the AKT phosphorylation, effectively suppressed the proliferation of RAD-R cells while treatment with palbociclib had no effect.

Conclusion: Among the many signaling transduction pathways, which are altered post everolimus resistance, targeting dual mTORC1/2 is a possible option for patients who have recurrent disease from previous everolimus treatment.

Keywords: AI resistance; Everolimus; MLN0128; MTOR inhibitors.

MeSH terms

  • Benzoxazoles / pharmacology*
  • Biomarkers
  • Breast Neoplasms / metabolism*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Drug Resistance, Neoplasm*
  • Everolimus / pharmacology*
  • Female
  • Humans
  • Inhibitory Concentration 50
  • Phosphorylation / drug effects
  • Protein Kinase Inhibitors / pharmacology*
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism
  • Pyrimidines / pharmacology*
  • Receptors, Estrogen / metabolism
  • Signal Transduction / drug effects
  • TOR Serine-Threonine Kinases / antagonists & inhibitors*

Substances

  • Benzoxazoles
  • Biomarkers
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Receptors, Estrogen
  • Everolimus
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • sapanisertib