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新型铂类治疗药物通过触发细胞内 ROS 风暴诱导癌细胞快速死亡。

Novel platinum therapeutics induce rapid cancer cell death through triggering intracellular ROS storm.

机构信息

Department of Nanomedicine, Houston Methodist Academic Institute, Houston, TX, 77030, USA.

Department of Nanomedicine, Houston Methodist Academic Institute, Houston, TX, 77030, USA.

出版信息

Biomaterials. 2025 Mar;314:122835. doi: 10.1016/j.biomaterials.2024.122835. Epub 2024 Sep 11.

Abstract

Induction of reactive oxygen species (ROS) production in cancer cells plays a critical role for cancer treatment. However, therapeutic efficiency remains challenging due to insufficient ROS production of current ROS inducers. We designed a novel platinum (Pt)-based drug named "carrier-platin" that integrates ultrasmall Pt-based nanoparticles uniformly confined within a poly(amino acids) carrier. Carrier-platin dramatically triggered a burst of ROS in cancer cells, leading to cancer cell death as quick as 30 min. Unlike traditional Pt-based drugs which induce cell apoptosis through DNA intercalation, carrier-platin with superior ROS catalytic activities induces a unique pattern of cancer cell death that is neither apoptosis nor ferroptosis and operates independently of DNA damage. Importantly, carrier-platin demonstrates superior anti-tumor efficacy against a broad spectrum of cancers, particularly those with multidrug resistance, while maintaining minimal systemic toxicity. Our findings reveal a distinct mechanism of action of Pt in cancer cell eradication, positioning carrier-platin as a novel category of anti-cancer chemotherapeutics.

摘要

诱导癌细胞中活性氧 (ROS) 的产生对于癌症治疗至关重要。然而,由于当前 ROS 诱导剂产生的 ROS 不足,治疗效率仍然具有挑战性。我们设计了一种新型基于铂 (Pt) 的药物,名为“载体铂”,它将超小的基于 Pt 的纳米颗粒均匀地限制在聚(氨基酸)载体中。载体铂在癌细胞中剧烈引发 ROS 的爆发,导致癌细胞在短短 30 分钟内死亡。与通过 DNA 插入诱导细胞凋亡的传统基于 Pt 的药物不同,具有优异 ROS 催化活性的载体铂诱导一种独特的癌细胞死亡模式,既不是细胞凋亡也不是铁死亡,并且独立于 DNA 损伤。重要的是,载体铂对广泛的癌症具有优异的抗肿瘤功效,特别是对多药耐药的癌症,同时保持最小的全身毒性。我们的研究结果揭示了 Pt 在癌细胞清除中的独特作用机制,使载体铂成为一种新型的抗癌化疗药物。

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Advances in Delivering Oxidative Modulators for Disease Therapy.用于疾病治疗的氧化调节剂递送进展。
Research (Wash D C). 2022 Sep 21;2022:9897464. doi: 10.34133/2022/9897464. eCollection 2022.

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