Biodegradable calcium sulfide-based nanomodulators for H2S-boosted Ca2+-involved synergistic cascade cancer therapy

化学 细胞内 线粒体 过氧化氢酶 细胞生物学 钙 HMOX1型 生物学中的钙 氧化应激 生物化学 生物物理学 癌症研究 药理学 生物 酶 有机化学 血红素 血红素加氧酶
作者
Chuchu Lin,Chenyi Huang,Zhaoqing Shi,Meitong Ou,Shengjie Sun,Mian Yu,Ting Chen,Yunfei Yi,Xiaoyuan Ji,Feng Lv,Meiying Wu,Lin Mei
出处
期刊:Acta Pharmaceutica Sinica B [Elsevier BV]
卷期号:12 (12): 4472-4485 被引量:55
标识
DOI:10.1016/j.apsb.2022.08.008
摘要

Hydrogen sulfide (H2S) is the most recently discovered gasotransmitter molecule that activates multiple intracellular signaling pathways and exerts concentration-dependent antitumor effect by interfering with mitochondrial respiration and inhibiting cellular ATP generation. Inspired by the fact that H2S can also serve as a promoter for intracellular Ca2+ influx, tumor-specific nanomodulators (I-CaS@PP) have been constructed by encapsulating calcium sulfide (CaS) and indocyanine green (ICG) into methoxy poly (ethylene glycol)-b-poly (lactide-co-glycolide) (PLGA-PEG). I-CaS@PP can achieve tumor-specific biodegradability with high biocompatibility and pH-responsive H2S release. The released H2S can effectively suppress the catalase (CAT) activity and synergize with released Ca2+ to facilitate abnormal Ca2+ retention in cells, thus leading to mitochondria destruction and amplification of oxidative stress. Mitochondrial dysfunction further contributes to blocking ATP synthesis and downregulating heat shock proteins (HSPs) expression, which is beneficial to overcome the heat endurance of tumor cells and strengthen ICG-induced photothermal performance. Such a H2S-boosted Ca2+-involved tumor-specific therapy exhibits highly effective tumor inhibition effect with almost complete elimination within 14-day treatment, indicating the great prospect of CaS-based nanomodulators as antitumor therapeutics.
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