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降低NLRP3炎性小体激活在阿霉素心脏毒性中的有益作用及其抗癌作用。

The beneficial effects of reducing NLRP3 inflammasome activation in the cardiotoxicity and the anti-cancer effects of doxorubicin.

作者信息

Maayah Zaid H, Takahara Shingo, Dyck Jason R B

机构信息

Cardiovascular Research Centre, Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada.

458 Heritage Medical Research Centre, University of Alberta, Edmonton, AB, T6G 2S2, Canada.

出版信息

Arch Toxicol. 2021 Jan;95(1):1-9. doi: 10.1007/s00204-020-02876-2. Epub 2020 Aug 27.

Abstract

Doxorubicin (DOX) is a powerful broad-spectrum anti-neoplastic anthracycline antibiotic. However, DOX may cause a dose-dependent cardiotoxicity that can eventually progress to congestive heart failure and death. Numerous molecular mechanisms have been implicated in the cardiotoxic effect of DOX including topoisomerase IIβ and generation of free radicals. However, targeting these pathways appears to be insufficient to mitigate the cardiotoxic effects of DOX and/or ultimately reduces the anti-tumor activity of DOX. Thus, there remains a crucial need to identify novel pharmacological targets that can alleviate the cardiotoxic effects of DOX without reducing its anti-tumor activity. Recent studies have suggested that the Nucleotide-Binding Domain-Like Receptor Protein 3 (NLRP3) inflammasome is implicated in tumor progression and the chemoresistance of cancer cells to DOX. Of interest, reducing NLRP3 inflammasome activity alleviates DOX-induced cardiotoxicity. Therefore, we postulate that strategies that target the NLRP3 inflammasome can help mitigate the cardiotoxic effects of DOX while maintaining and/or even enhancing its anti-cancer activity. Herein, we review the current knowledge about the potential implication of the NLRP3 inflammasome in the anti-cancer and cardiotoxic effects of DOX.

摘要

阿霉素(DOX)是一种强效的广谱抗肿瘤蒽环类抗生素。然而,DOX可能会导致剂量依赖性心脏毒性,最终可能发展为充血性心力衰竭并导致死亡。DOX的心脏毒性作用涉及多种分子机制,包括拓扑异构酶IIβ和自由基的产生。然而,针对这些途径似乎不足以减轻DOX的心脏毒性作用和/或最终降低DOX的抗肿瘤活性。因此,仍然迫切需要确定新的药理学靶点,这些靶点可以减轻DOX的心脏毒性作用而不降低其抗肿瘤活性。最近的研究表明,核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)炎性小体与肿瘤进展以及癌细胞对DOX的化疗耐药性有关。有趣的是,降低NLRP3炎性小体活性可减轻DOX诱导的心脏毒性。因此,我们推测,靶向NLRP3炎性小体的策略有助于减轻DOX的心脏毒性作用,同时维持和/或甚至增强其抗癌活性。在此,我们综述了目前关于NLRP3炎性小体在DOX的抗癌和心脏毒性作用中潜在影响的知识。

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