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近期关于对抗阿霉素诱导毒性的十年进展

A recent decade update on combating doxorubicin-induced toxicities.

作者信息

Sritharan Sruthi, Sivalingam Nageswaran

机构信息

Department of Biotechnology, School of Bioengineering, College of Engineering and Technology, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu District, Tamil Nadu, 603203, India.

出版信息

Arch Toxicol. 2025 Jul 2. doi: 10.1007/s00204-025-04112-1.

DOI:10.1007/s00204-025-04112-1
PMID:40600983
Abstract

The gradual rise in global cancer rates every year instills the need for a reliable therapeutic strategy. Chemotherapy alone or in combination with surgery, radiation, or adjuvant therapy is still the preferred treatment option for a wide range of cancers. Doxorubicin (dox) is an extensively used chemotherapeutic anthracycline for combating a broad range of solid and soft-tissue tumors. However, dox therapy is often associated with undesirable side effects, mainly cardiotoxicity, limiting its clinical application. Over the years, many strategies have been developed to overcome these toxicities and improve the drug's therapeutic potential. This review is focused on discussing the recent investigations into natural compounds, nanoformulations, miRNAs, and physical exercise in protecting against dox-mediated cardiotoxicity, hepatotoxicity, nephrotoxicity, and neurotoxicity.

摘要

全球癌症发病率逐年逐渐上升,这凸显了对可靠治疗策略的需求。单独化疗或与手术、放疗或辅助治疗联合使用,仍然是多种癌症的首选治疗方案。阿霉素(dox)是一种广泛使用的化疗蒽环类药物,用于对抗多种实体和软组织肿瘤。然而,阿霉素治疗常常伴有不良副作用,主要是心脏毒性,这限制了其临床应用。多年来,人们已开发出许多策略来克服这些毒性并提高该药物的治疗潜力。本综述重点讨论了关于天然化合物、纳米制剂、微小RNA以及体育锻炼在预防阿霉素介导的心脏毒性、肝毒性、肾毒性和神经毒性方面的最新研究。

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1
A recent decade update on combating doxorubicin-induced toxicities.近期关于对抗阿霉素诱导毒性的十年进展
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2
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本文引用的文献

1
Self-assembled doxorubicin prodrug riding on the albumin express train enable tumor targeting and bio-activation.搭载白蛋白“快车”的自组装阿霉素前药可实现肿瘤靶向和生物激活。
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Natural epigallocatechin-3-gallocarboxylate nanoformulation loaded doxorubicin to construct a novel and low cardiotoxicity chemotherapeutic drug for high-efficiency breast cancer therapy.负载表没食子儿茶素-3-没食子酸酯的纳米制剂载多柔比星,构建一种新型低心脏毒性的化疗药物用于高效乳腺癌治疗。
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Extract Mitigates Doxorubicin-Induced Hepatotoxicity in Male Rats.
提取物减轻阿霉素诱导的雄性大鼠肝毒性。
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Oxyresveratrol and/or Dapagliflozin Attenuate Doxorubicin-Induced Nephrotoxicity via Modulation of PPAR-γ/Nrf-2/HO-1, NF-κB/TNF-α/Keap-1, and Bcl-2/Caspase-3/ATG-5 signaling pathways in rats.氧化白藜芦醇和/或达格列净通过调节大鼠体内的PPAR-γ/Nrf-2/HO-1、NF-κB/TNF-α/Keap-1以及Bcl-2/Caspase-3/ATG-5信号通路减轻阿霉素诱导的肾毒性。
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Novel PLGA-based nanoformulation decreases doxorubicin-induced cardiotoxicity.新型 PLGA 纳米制剂可降低阿霉素所致心脏毒性。
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8
Evaluate the in vitro effect of anthracycline and alkylating cytophosphane chemotherapeutics on dopaminergic neurons.评价蒽环类和烷化细胞毒化疗药物对多巴胺能神经元的体外作用。
Cancer Rep (Hoboken). 2024 Apr;7(4):e2074. doi: 10.1002/cnr2.2074.
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Eriodictyol attenuates doxorubicin-induced nephropathy by activating the AMPK/Nrf2 signalling pathway.圣草酚通过激活AMPK/Nrf2信号通路减轻阿霉素诱导的肾病。
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10
Cationic Vitamin E-TPGS Mixed Micelles of Berberine to Neutralize Doxorubicin-Induced Cardiotoxicity via Amelioration of Mitochondrial Dysfunction and Impeding Apoptosis.小檗碱的阳离子维生素E-TPGS混合胶束通过改善线粒体功能障碍和抑制细胞凋亡来中和阿霉素诱导的心脏毒性。
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