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Combination treatment with doxorubicin and gamitrinib synergistically augments anticancer activity through enhanced activation of Bim

机译:阿霉素和加米替尼联合治疗可通过增强Bim的激活来协同增强抗癌活性

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摘要

Background: A common approach to cancer therapy in clinical practice is the combination of several drugs to boost the anticancer activity of available drugs while suppressing their unwanted side effects. In this regard, we examined the efficacy of combination treatment with the widely-used genotoxic drug doxorubicin and the mitochondriotoxic Hsp90 inhibitor gamitrinib to exploit disparate stress signaling pathways for cancer therapy.Methods: The cytotoxicity of the drugs as single agents or in combination against several cancer cell types was analyzed by MTT assay and the synergism of the drug combination was evaluated by calculating the combination index. To understand the molecular mechanism of the drug synergism, stress signaling pathways were analyzed after drug combination. Two xenograft models with breast and prostate cancer cells were used to evaluate anticancer activity of the drug combination in vivo. Cardiotoxicity was assessed by tissue histology and serum creatine phosphokinase concentration.Results: Gamitrinib sensitized various human cancer cells to doxorubicin treatment, and combination treatment with the two drugs synergistically increased apoptosis. The cytotoxicity of the drug combination involved activation and mitochondrial accumulation of the proapoptotic Bcl-2 family member Bim. Activation of Bim was associated with increased expression of the proapoptotic transcription factor C/EBP-homologous protein and enhanced activation of the stress kinase c-Jun N-terminal kinase. Combined drug treatment with doxorubicin and gamitrinib dramatically reduced in vivo tumor growth in prostate and breast xenograft models without increasing cardiotoxicity.Conclusions: The drug combination showed synergistic anticancer activities toward various cancer cells without aggravating the cardiotoxic side effects of doxorubicin, suggesting that the full therapeutic potential of doxorubicin can be unleashed through combination with gamitrinib.
机译:背景:临床实践中一种常见的癌症治疗方法是几种药物的组合,以增强现有药物的抗癌活性,同时抑制其不良副作用。在这方面,我们研究了广泛使用的遗传毒性药物阿霉素和线粒体毒性Hsp90抑制剂加米替尼联合治疗利用不同的应激信号通路进行癌症治疗的功效。通过MTT分析法分析癌细胞类型,并通过计算组合指数评价药物组合的协同作用。为了了解药物协同作用的分子机制,在药物组合后分析了应激信号通路。使用具有乳腺癌和前列腺癌细胞的两种异种移植模型来评估该药物组合在体内的抗癌活性。通过组织组织学和血清肌酸磷酸激酶浓度评估心脏毒性。结果:加米替尼使各种人类癌细胞对阿霉素治疗敏感,并与两种药物联合治疗协同增加细胞凋亡。药物组合的细胞毒性涉及促凋亡的Bcl-2家族成员Bim的激活和线粒体积累。 Bim的激活与促凋亡转录因子C / EBP同源蛋白的表达增加和应激激酶c-Jun N端激酶的激活增强有关。阿霉素和加米替尼联合药物治疗可显着降低前列腺和乳腺异种移植模型的体内肿瘤生长,而不会增加心脏毒性。与加米替尼联合使用可释放阿霉素的潜力。

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