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Effects and mechanism of arsenic trioxide in combination with rmhTRAIL in multiple myeloma

机译:三氧化二砷联合rmhTRAIL治疗多发性骨髓瘤的作用及其机制

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The anti-tumor potential of arsenic trioxide (ATO) and recombinant mutant human TRAIL (rmhTRAIL) has been confirmed in various kinds of tumors. However, the effects and mechanism of the two drugs in combination in multiple myeloma (MM) have not been established. In this study, we evaluated the proliferation inhibition and apoptosis induction effects of ATO and rmhTRAIL as single agents and in combination on the MM cell lines RPMI8226 and U266. Then, we used high-performance liquid chromatography and mass spectrometry to find differentially expressed proteins before and after drug treatment and to analyze the mechanism underlying the effect of ATO and rmhTRAIL on MM cells. Results indicated that ATO and rmhTRAIL had synergistic or additive effects on proliferation inhibition and apoptosis induction in MM cells, and the mechanism underlying the two-drug combination might involve regulation of the expression of several proteins affected by ATO and rmhTRAIL. Our study provides evidence of a potential new combination treatment strategy for MM. Copyright (C) 2016 ISEH - International Society for Experimental Hematology. Published by Elsevier Inc.
机译:三氧化二砷(ATO)和重组突变型人TRAIL(rmhTRAIL)的抗肿瘤潜力已在各种肿瘤中得到证实。但是,尚未确定两种药物联合治疗多发性骨髓瘤(MM)的作用和机制。在这项研究中,我们评估了ATO和rmhTRAIL作为单一药物以及联合使用对MM细胞系RPMI8226和U266的增殖抑制和凋亡诱导作用。然后,我们使用高效液相色谱和质谱法在药物处理前后发现差异表达的蛋白质,并分析了ATO和rmhTRAIL对MM细胞作用的潜在机制。结果表明,ATO和rmhTRAIL对MM细胞的增殖抑制和凋亡诱导具有协同或累加作用,两种药物组合的潜在机制可能涉及调节受ATO和rmhTRAIL影响的几种蛋白质的表达。我们的研究提供了潜在的新的MM联合治疗策略的证据。版权所有(C)2016 ISEH-国际实验血液学会。由Elsevier Inc.发布

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