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破坏铁稳态以诱导铁死亡,用白蛋白包裹的铂(IV)纳米药物治疗非小细胞肺癌

Disruption of Iron Homeostasis to Induce Ferroptosis with Albumin-Encapsulated Pt(IV) Nanodrug for the Treatment of Non-Small Cell Lung Cancer.

作者信息

Tian Hui-Xiang, Mei Jie, Cao Lei, Song Jianan, Rong Dingchao, Fang Man, Xu Zhe, Chen Juan, Tang Jie, Xiao Haihua, Liu Zhaoqian, Wang Peng-Yuan, Yin Ji-Ye, Li Xiang-Ping

机构信息

Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, 410008, China.

School of Bioscience and Bioengineering, South China University of Technology, Guangzhou, 510006, China.

出版信息

Small. 2023 Dec;19(49):e2206688. doi: 10.1002/smll.202206688. Epub 2023 Aug 22.

Abstract

Non-small cell lung cancer (NSCLC) is the most common pathological type of lung cancer , accounting for approximately 85% of lung cancers. For more than 40 years, platinum (Pt)-based drugs are still one of the most widely used anticancer drugs even in the era of precision medicine and immunotherapy. However, the clinical limitations of Pt-based drugs, such as serious side effects and drug resistance, have not been well solved. This study constructs a new albumin-encapsulated Pt(IV) nanodrug (HSA@Pt(IV)) based on the Pt(IV) drug and nanodelivery system. The characterization of nanodrug and biological experiments demonstrate its excellent drug delivery and antitumor effects. The multi-omics analysis of the transcriptome and the ionome reveals that nanodrug can activate ferroptosis by affecting intracellular iron homeostasis in NSCLC. This study provides experimental evidence to suggest the potential of HSA@Pt(IV) as a nanodrug with clinical application.

摘要

非小细胞肺癌(NSCLC)是肺癌最常见的病理类型,约占肺癌的85%。40多年来,即使在精准医学和免疫治疗时代,铂(Pt)类药物仍是使用最广泛的抗癌药物之一。然而,铂类药物的临床局限性,如严重的副作用和耐药性,尚未得到很好的解决。本研究基于铂(IV)药物和纳米递送系统构建了一种新型白蛋白包裹的铂(IV)纳米药物(HSA@Pt(IV))。纳米药物的表征和生物学实验证明了其优异的药物递送和抗肿瘤效果。转录组和离子组的多组学分析表明,纳米药物可通过影响NSCLC细胞内铁稳态激活铁死亡。本研究提供了实验证据,表明HSA@Pt(IV)作为一种具有临床应用潜力的纳米药物。

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