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Biodegradable calcium sulfide-based nanomodulators for H(2)S-boosted Ca(2+)-involved synergistic cascade cancer therapy

Hydrogen sulfide (H(2)S) 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 th...

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Detalles Bibliográficos
Autores principales: Lin, Chuchu, Huang, Chenyi, Shi, Zhaoqing, Ou, Meitong, Sun, Shengjie, Yu, Mian, Chen, Ting, Yi, Yunfei, Ji, Xiaoyuan, Lv, Feng, Wu, Meiying, Mei, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764068/
https://www.ncbi.nlm.nih.gov/pubmed/36561996
http://dx.doi.org/10.1016/j.apsb.2022.08.008
Descripción
Sumario:Hydrogen sulfide (H(2)S) 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 H(2)S can also serve as a promoter for intracellular Ca(2+) 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 H(2)S release. The released H(2)S can effectively suppress the catalase (CAT) activity and synergize with released Ca(2+) to facilitate abnormal Ca(2+) 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 H(2)S-boosted Ca(2+)-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.