Ivermectin Synergizes with Modulated Electro-hyperthermia and Improves Its Anticancer Effects in a Triple-Negative Breast Cancer Mouse Model.
Kenan AlossPedro Henrique Leroy VianaSyeda Mahak Zahra BokhariNino GiunashviliCsaba András SchvarczDániel BócsiZoltán KoósZoltán BenyóPeter HamarPublished in: ACS pharmacology & translational science (2024)
Triple-negative breast cancer (TNBC) is the most aggressive breast cancer subtype, with limited treatment options. Modulated electro-hyperthermia (mEHT) is a novel adjuvant cancer therapy that induces selective cancer damage. However, mEHT upregulates heat shock protein beta 1 (HSPB1), a cancer-promoting stress chaperone molecule. Thus, we investigated whether ivermectin (IVM), an anthelmintic drug, may synergize with mEHT and enhance its anticancer effects by inhibiting HSPB1 phosphorylation. Isogenic 4T1 TNBC cells were inoculated into BALB/c mice and treated with mEHT, IVM, or a combination of both. IVM synergistically improved the tumor growth inhibition achieved by mEHT. Moreover, IVM downregulated mEHT-induced HSPB1 phosphorylation. Thus, the strongest cancer tissue damage was observed in the mEHT + IVM-treated tumors, coupled with the strongest apoptosis induction and proliferation inhibition. In addition, there was no significant body weight loss in mice treated with mEHT and IVM, indicating that this combination was well-tolerated. In conclusion, mEHT combined with IVM is a new, effective, and safe option for the treatment of TNBC.
Keyphrases
- heat shock protein
- papillary thyroid
- heat shock
- oxidative stress
- cancer therapy
- squamous cell
- weight loss
- mouse model
- cell cycle arrest
- induced apoptosis
- cell death
- early stage
- drug delivery
- lymph node metastasis
- childhood cancer
- endoplasmic reticulum stress
- drug induced
- squamous cell carcinoma
- high speed
- newly diagnosed
- type diabetes
- young adults
- diabetic rats
- insulin resistance
- skeletal muscle
- electronic health record
- high resolution
- atomic force microscopy
- adverse drug
- protein kinase