1. Academic Validation
  2. Everolimus selectively targets vemurafenib resistant BRAFV600E melanoma cells adapted to low pH

Everolimus selectively targets vemurafenib resistant BRAFV600E melanoma cells adapted to low pH

  • Cancer Lett. 2017 Nov 1;408:43-54. doi: 10.1016/j.canlet.2017.08.010.
Jessica Ruzzolini 1 Silvia Peppicelli 1 Elena Andreucci 1 Francesca Bianchini 1 Francesca Margheri 1 Anna Laurenzana 1 Gabriella Fibbi 1 Nicola Pimpinelli 2 Lido Calorini 3
Affiliations

Affiliations

  • 1 Department of Experimental and Clinical Biomedical Sciences "Mario Serio", Section of Experimental Pathology and Oncology, University of Florence, Italy.
  • 2 Department of Surgery and Translational Medicine (DCMT), University of Florence, Italy.
  • 3 Department of Experimental and Clinical Biomedical Sciences "Mario Serio", Section of Experimental Pathology and Oncology, University of Florence, Italy; Istituto Toscano Tumori, Center of Excellence for the Study at Molecular and Clinical Level of Chronic, Degenerative and Neoplastic Diseases to Develop Novel Therapies (DENOTHE), Italy. Electronic address: lido.calorini@unifi.it.
Abstract

Vemurafenib, a BRaf Inhibitor, elicits in ∼80% of BRafV600E-mutant melanoma patients a transient anti-tumor response which precedes the emergence of resistance. We tested whether an acidic tumor microenvironment may favor a BRaf Inhibitor resistance. A375M6 BRafV600E melanoma cells, either exposed for a short period or chronically adapted to an acidic medium, showed traits compatible with an epithelial-mesenchymal transition, reduced proliferation and high resistance to Apoptosis. Both types of acidic cells treated with vemurafenib did not change their proliferation, distribution in cell cycle and level of p-AKT, in contrast to cells grown at standard pH, which showed reduced proliferation, cell cycle arrest and ERK/Akt inhibition. Even after treatment with trametinib (MEK Inhibitor) acidic cell features did not change. Then, since both types of acidic cells exhibited high p-p70S6K, i.e. active mTOR signaling, we tested everolimus, an mTOR Inhibitor, which was efficient in inducing Apoptosis in acidic cells without affecting melanoma cells grown at standard pH. Our results indicate that an acidic microenvironment may cooperate in inducing a BRaf Inhibitor resistance in melanoma cells and a combined therapy with everolimus could be used to overcome that resistance.

Keywords

Acidosis; BRAF(V600E) melanoma cells; Everolimus; Trametinib; Tumor microenvironment; Vemurafenib.

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