Experimental and computational assessment of the synergistic pharmacodynamic drug-drug interactions of a triple combination therapy in refractory HER2-positive breast cancer cells

J Pharmacokinet Pharmacodyn. 2022 Apr;49(2):227-241. doi: 10.1007/s10928-021-09795-4. Epub 2021 Nov 13.

Abstract

The development of innate and/or acquired resistance to human epidermal growth factor receptor type-2 (HER2)-targeted therapy in HER2-positive breast cancer (HER2 + BC) is a major clinical challenge that needs to be addressed. One of the main mechanisms of resistance includes aberrant activation of the HER2 and phosphatidylinositol 3-kinase/AKT8 virus oncogene cellular homolog/mammalian target of rapamycin (PI3K/Akt/mTOR) pathways. In the present work, we propose to use a triple combination therapy to combat this resistance phenomenon. Our strategy involves evaluation of two targeted small molecule agents, everolimus and dasatinib, with complementary inhibitory circuitries in the PI3K/Akt/mTOR pathway, along with a standard cytotoxic agent, paclitaxel. Everolimus inhibits mTOR, while dasatinib inhibits Src, which is a protein upstream of Akt. An over-activation of these two proteins has been implicated in approximately 50% of HER2 + BC cases. Hence, we hypothesize that their simultaneous inhibition may lead to enhanced cell-growth inhibition. Moreover, the potent apoptotic effects of paclitaxel may help augment the overall cytotoxicity of the proposed triple combination in HER2 + BC cells. To this end, we investigated experimentally and assessed computationally the in vitro pharmacodynamic drug-drug interactions of the various dual and triple combinations to assess their subsequent combinatorial effects (synergistic/additive/antagonistic) in a HER2-therapy resistant BC cell line, JIMT-1. Our proposed triple combination therapy demonstrated synergism in JIMT-1 cells, thus corroborating our hypothesis. This effort may form the basis for further investigation of the triple combination therapy in vivo at a mechanistic level in HER2-therapy resistant BC cells.

Keywords: Breast cancer; Drug–drug interactions; HER2-therapy resistance; Pharmacodynamics.

MeSH terms

  • Antineoplastic Agents* / pharmacology
  • Antineoplastic Agents* / therapeutic use
  • Breast Neoplasms* / drug therapy
  • Breast Neoplasms* / metabolism
  • Cell Line, Tumor
  • Dasatinib / pharmacology
  • Dasatinib / therapeutic use
  • Drug Interactions
  • Drug Resistance, Neoplasm
  • Everolimus / pharmacology
  • Everolimus / therapeutic use
  • Female
  • Humans
  • Paclitaxel / pharmacology
  • Phosphatidylinositol 3-Kinases / pharmacology
  • Phosphatidylinositol 3-Kinases / therapeutic use
  • Proto-Oncogene Proteins c-akt / metabolism
  • Proto-Oncogene Proteins c-akt / pharmacology
  • Receptor, ErbB-2
  • TOR Serine-Threonine Kinases / metabolism
  • Trastuzumab / therapeutic use

Substances

  • Antineoplastic Agents
  • Everolimus
  • Receptor, ErbB-2
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • Trastuzumab
  • Paclitaxel
  • Dasatinib