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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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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 |
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author | Lin, Chuchu Huang, Chenyi Shi, Zhaoqing Ou, Meitong Sun, Shengjie Yu, Mian Chen, Ting Yi, Yunfei Ji, Xiaoyuan Lv, Feng Wu, Meiying Mei, Lin |
author_facet | Lin, Chuchu Huang, Chenyi Shi, Zhaoqing Ou, Meitong Sun, Shengjie Yu, Mian Chen, Ting Yi, Yunfei Ji, Xiaoyuan Lv, Feng Wu, Meiying Mei, Lin |
author_sort | Lin, Chuchu |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9764068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-97640682022-12-21 Biodegradable calcium sulfide-based nanomodulators for H(2)S-boosted Ca(2+)-involved synergistic cascade cancer therapy Lin, Chuchu Huang, Chenyi Shi, Zhaoqing Ou, Meitong Sun, Shengjie Yu, Mian Chen, Ting Yi, Yunfei Ji, Xiaoyuan Lv, Feng Wu, Meiying Mei, Lin Acta Pharm Sin B Original Article 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. Elsevier 2022-12 2022-08-19 /pmc/articles/PMC9764068/ /pubmed/36561996 http://dx.doi.org/10.1016/j.apsb.2022.08.008 Text en © 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Lin, Chuchu Huang, Chenyi Shi, Zhaoqing Ou, Meitong Sun, Shengjie Yu, Mian Chen, Ting Yi, Yunfei Ji, Xiaoyuan Lv, Feng Wu, Meiying Mei, Lin Biodegradable calcium sulfide-based nanomodulators for H(2)S-boosted Ca(2+)-involved synergistic cascade cancer therapy |
title | Biodegradable calcium sulfide-based nanomodulators for H(2)S-boosted Ca(2+)-involved synergistic cascade cancer therapy |
title_full | Biodegradable calcium sulfide-based nanomodulators for H(2)S-boosted Ca(2+)-involved synergistic cascade cancer therapy |
title_fullStr | Biodegradable calcium sulfide-based nanomodulators for H(2)S-boosted Ca(2+)-involved synergistic cascade cancer therapy |
title_full_unstemmed | Biodegradable calcium sulfide-based nanomodulators for H(2)S-boosted Ca(2+)-involved synergistic cascade cancer therapy |
title_short | Biodegradable calcium sulfide-based nanomodulators for H(2)S-boosted Ca(2+)-involved synergistic cascade cancer therapy |
title_sort | biodegradable calcium sulfide-based nanomodulators for h(2)s-boosted ca(2+)-involved synergistic cascade cancer therapy |
topic | Original Article |
url | 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 |
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