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

被引:4
|
作者
Ju, Donghong [1 ]
Xie, Youming [1 ]
机构
[1] Wayne State Univ, Karmanos Canc Inst, Dept Pathol & Oncol, Sch Med, Detroit, MI 48201 USA
关键词
proteasome; proteasome inhibitor; combined therapy; myeloma; dyclonine; BREAST-CANCER CELLS; SACCHAROMYCES-CEREVISIAE; THERAPY; PATHWAY; YEAST; RESISTANCE; EXPRESSION; NETWORK;
D O I
10.3892/mmr.2014.2522
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:2609 / 2612
页数:4
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