近红外激活型抗癌顺铂(IV)复合物以非依赖于氧的方式直接光氧化生物分子。

Near-infrared-activated anticancer platinum(IV) complexes directly photooxidize biomolecules in an oxygen-independent manner.

机构信息

Department of Chemistry, City University of Hong Kong, Hong Kong SAR, P. R. China.

City University of Hong Kong Shenzhen Research Institute, Shenzhen, P. R. China.

出版信息

Nat Chem. 2023 Jul;15(7):930-939. doi: 10.1038/s41557-023-01242-w. Epub 2023 Jun 22.

Abstract

Conventional light-driven cancer therapeutics require oxygen and visible light to indirectly damage biomolecules, limiting their efficacy in deep, hypoxic tumours. Here we report the use of near-infrared-activated small-molecule Pt(IV) photooxidants to directly oxidize intracellular biomolecules in an oxygen-independent manner, achieving controllable and effective elimination of cancer stem cells. These Pt(IV) complexes accumulate in the endoplasmic reticulum and show low toxicity in the dark. Upon irradiation, the resultant metal-enhanced photooxidation effect causes them to robustly photooxidize survival-related biomolecules, induce intense oxidative stress, disrupt intracellular pH (pHi) homeostasis and initiate nonclassical necrosis. In vivo experiments confirm that the lead photooxidant can effectively inhibit tumour growth, suppress metastasis and activate the immune system. Our study validates the concept of metal-enhanced photooxidation and the subsequent chemotherapeutic applications, supporting the development of such localized photooxidants to directly damage intracellular biomolecules and decrease pHi as a strategy for effective metal-based drugs.

摘要

传统的光驱动癌症治疗需要氧气和可见光来间接损伤生物分子,这限制了它们在深部缺氧肿瘤中的疗效。在这里,我们报告了使用近红外激活的小分子 Pt(IV)光氧化剂以非依赖于氧气的方式直接氧化细胞内生物分子,从而实现对癌症干细胞的可控和有效消除。这些 Pt(IV) 配合物在细胞质中积累,在黑暗中表现出低毒性。在照射下,产生的金属增强光氧化效应导致它们强烈地光氧化与生存相关的生物分子,诱导强烈的氧化应激,破坏细胞内 pH(pHi)稳态并引发非经典坏死。体内实验证实,先导光氧化剂能够有效地抑制肿瘤生长、抑制转移并激活免疫系统。我们的研究验证了金属增强光氧化的概念和随后的化疗应用,支持开发这种局部光氧化剂来直接损伤细胞内生物分子并降低 pHi 作为有效金属基药物的策略。

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