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Article

Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines

  • Authors:
    • Tomoko Takahashi
    • Naoko Abe
    • Hiroyuki Kanoh
    • Yoshiko Banno
    • Mariko Seishima
  • View Affiliations / Copyright

    Affiliations: Department of Dermatology, Gifu University Graduate School of Medicine, Gifu 501‑1194, Japan
  • Pages: 5151-5158
    |
    Published online on: October 8, 2018
       https://doi.org/10.3892/mmr.2018.9537
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Abstract

Vemurafenib, a selective inhibitor of mutated BRAF, is used to treat late‑stage melanoma. However, resistance to vemurafenib is urgently required as it can have fatal consequences. Fingolimod (FTY720), a sphingosine‑1‑phosphate receptor modulator, has been used for the treatment of several malignant neoplasms in clinical trials. The present study investigated the effects of FTY720 and vemurafenib combination treatment on cell death induction, and defined the molecular mechanisms in vemurafenib‑resistant melanoma cells. The combination treatment with FTY720 and vemurafenib reduced cell viability, and the expression of apoptosis‑associated cleaved poly (adenosine diphosphate‑ribose) polymerase (PARP) was increased when compared with treatment with vemurafenib alone in WM‑115 cells, a vemurafenib‑resistant human melanoma cell line. In addition, the protein expression of phosphorylated extracellular signal‑related kinase (ERK) in WM‑115 cells was decreased by this combination treatment. Vemurafenib‑resistant SK‑Mel‑28 cells (R‑SK‑Mel) were established by culturing SK‑Mel‑28 cells, which are the most sensitive to vemurafenib, in the presence of vemurafenib. Similar to WM‑155 cells, the viability of R‑SK‑Mel cells was reduced and the expression of cleaved PARP was increased by the combination treatment with FTY720 and vemurafenib. In addition, the expression of phosphorylated ERK and Akt was also reduced by this treatment. These results suggested that FTY720 and vemurafenib synergistically induced cell death by downregulating proliferation and survival signalling pathways in vemurafenib‑resistant melanoma cells.
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Copy and paste a formatted citation
Spandidos Publications style
Takahashi T, Abe N, Kanoh H, Banno Y and Seishima M: Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines. Mol Med Rep 18: 5151-5158, 2018.
APA
Takahashi, T., Abe, N., Kanoh, H., Banno, Y., & Seishima, M. (2018). Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines. Molecular Medicine Reports, 18, 5151-5158. https://doi.org/10.3892/mmr.2018.9537
MLA
Takahashi, T., Abe, N., Kanoh, H., Banno, Y., Seishima, M."Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines". Molecular Medicine Reports 18.6 (2018): 5151-5158.
Chicago
Takahashi, T., Abe, N., Kanoh, H., Banno, Y., Seishima, M."Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines". Molecular Medicine Reports 18, no. 6 (2018): 5151-5158. https://doi.org/10.3892/mmr.2018.9537
Copy and paste a formatted citation
x
Spandidos Publications style
Takahashi T, Abe N, Kanoh H, Banno Y and Seishima M: Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines. Mol Med Rep 18: 5151-5158, 2018.
APA
Takahashi, T., Abe, N., Kanoh, H., Banno, Y., & Seishima, M. (2018). Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines. Molecular Medicine Reports, 18, 5151-5158. https://doi.org/10.3892/mmr.2018.9537
MLA
Takahashi, T., Abe, N., Kanoh, H., Banno, Y., Seishima, M."Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines". Molecular Medicine Reports 18.6 (2018): 5151-5158.
Chicago
Takahashi, T., Abe, N., Kanoh, H., Banno, Y., Seishima, M."Synergistic effects of vemurafenib and fingolimod (FTY720) in vemurafenib‑resistant melanoma cell lines". Molecular Medicine Reports 18, no. 6 (2018): 5151-5158. https://doi.org/10.3892/mmr.2018.9537
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