Dyclonine enhances the cytotoxic effect of proteasome inhibitor bortezomib in multiple myeloma cells

  • Authors:
    • Donghong Ju
    • Youming Xie
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  • Published online on: August 28, 2014     https://doi.org/10.3892/mmr.2014.2522
  • Pages: 2609-2612
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Abstract

The proteasome has become an important target for cancer therapy with the approval of bortezomib for the treatment of relapsed/refractory multiple myeloma (MM). However, numerous patients with MM do not respond to bortezomib and those responding initially often acquire resistance. Recent clinical studies have also demonstrated that bortezomib is also inefficacious in the treatment of other types of cancer. Therefore, it is imperative to develop novel approaches and agents for proteasome-targeting cancer therapy. In the present study, it was revealed that dyclonine, a major component of the cough droplets Sucrets, markedly enhances the cytotoxic effects of bortezomib and minimizes drug resistance in MM cells. It was demonstrated that a combination of bortezomib and dyclonine markedly induced apoptosis of MM cells. The present study suggests a novel therapeutic use of an over‑the‑counter medicine for the treatment of MM.
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November-2014
Volume 10 Issue 5

Print ISSN: 1791-2997
Online ISSN:1791-3004

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Spandidos Publications style
Ju D and Ju D: Dyclonine enhances the cytotoxic effect of proteasome inhibitor bortezomib in multiple myeloma cells. Mol Med Rep 10: 2609-2612, 2014
APA
Ju, D., & Ju, D. (2014). Dyclonine enhances the cytotoxic effect of proteasome inhibitor bortezomib in multiple myeloma cells. Molecular Medicine Reports, 10, 2609-2612. https://doi.org/10.3892/mmr.2014.2522
MLA
Ju, D., Xie, Y."Dyclonine enhances the cytotoxic effect of proteasome inhibitor bortezomib in multiple myeloma cells". Molecular Medicine Reports 10.5 (2014): 2609-2612.
Chicago
Ju, D., Xie, Y."Dyclonine enhances the cytotoxic effect of proteasome inhibitor bortezomib in multiple myeloma cells". Molecular Medicine Reports 10, no. 5 (2014): 2609-2612. https://doi.org/10.3892/mmr.2014.2522