Synergistic Effects of Lenvatinib (E7080) and MEK Inhibitors against Anaplastic Thyroid Cancer in Preclinical Models.
Keisuke EnomotoShun HirayamaNaoko KumashiroXuefeng JingTakahito KimuraShunji TamagawaIbu MatsuzakiShin-Ichi MurataMuneki HotomiPublished in: Cancers (2021)
E7080, known as lenvatinib, is an oral multitargeted tyrosine kinase inhibitor that has been shown to improve the survival rate of patients with radioiodine-refractory thyroid cancer. However, a majority of patients do not continue lenvatinib intake due to disease progression or significant toxicity. To improve treatment success rates, we propose the combination of lenvatinib with mitogen-activated protein kinase (MEK) inhibitors. To test this hypothesis, we tested the effects of lenvatinib with the MEK inhibitor U0126 in vitro using two human anaplastic thyroid cancer (ATC) cell lines, 8505C and TCO1, and with another MEK inhibitor, selumetinib (AZD6244), in an ATC mouse model. We found that the combination of lenvatinib with MEK inhibitors enhanced the antitumor effects of monotherapy with either agent in vitro and in vivo, and these effects may be through the AKT (Protein Kinase B) and extracellular signal-regulated kinase (ERK) signaling pathways. Furthermore, the combination does not have significant adverse effects in the ATC mouse models in terms of body weight, blood biochemical parameters, and histopathology. In conclusion, the combination of lenvatinib with an MEK inhibitor is a potentially viable therapeutic approach for ATC treatment.
Keyphrases
- pi k akt
- signaling pathway
- mouse model
- protein kinase
- body weight
- cell proliferation
- end stage renal disease
- endothelial cells
- ejection fraction
- newly diagnosed
- combination therapy
- chronic kidney disease
- tyrosine kinase
- prognostic factors
- transcription factor
- patient reported outcomes
- stem cells
- epithelial mesenchymal transition
- drug delivery
- weight loss
- patient reported
- open label
- cancer therapy