期刊
SMALL
卷 17, 期 8, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202006599
关键词
cancer therapy; nanostructures; pyroptosis; spiky surface; tumor-activatable pyroptotic agents
类别
资金
- National Key Research and Development Program of China [2016YFA0203600]
- National Natural Science Foundation of China [31822019, 32071374, 51703195, 91859116]
- One Belt and One Road International Cooperation Project from Key Research and Development Program of Zhejiang Province [2019C04024]
- Zhejiang Provincial Natural Science Foundation of China [LGF19C100002]
- Fundamental Research Funds for the Central Universities [2018QNA7020, 2019XZZX004-15]
- National Science & Technology Major Project Key New Drug Creation and Manufacturing Program [2018ZX09711002]
- Postgraduate Research & Practice Innovation Program of Jiangsu Province [SJCX19-0318]
The study presents a virus-spike tumor-activatable pyroptotic agent for cancer-specific therapy, which can induce pyroptosis in tumor cells. This agent can accumulate in tumors after systemic administration and be degraded by intracellular glutathione to activate inflammasomes and lead to pyroptotic cell death. This structure-dependent and tumor intracellular GSH activatable pyroptotic agent represents a novel paradigm for cancer-specific pyroptotic nanomedicine development.
Invoking the occurrence of pyroptosis is an emerging strategy for the treatment of cancer. However, the practical applications of pyroptosis for cancer therapy are currently hindered due to the lack of tumor-specific and efficient pyroptotic agents in vivo. Herein, a virus-spike tumor-activatable pyroptotic agent (VTPA) for cancer-specific therapy is reported. The VTPA is composed of an organosilica coated iron oxide nanoparticle core and spiky manganese dioxide protrusions, which can readily accumulate in tumor after systemic administration, facilitate the tumor intracellular lysosomal rupture, and be degraded by tumor over-expressed intracellular glutathione (GSH) to release Mn ions and iron oxide nanoparticles (IONPs) for the synergetic activation of nucleotide binding oligomerization domain-like receptors protein 3 (NLRP3) inflammasomes. Consequently, the activation of NLRP3 inflammasomes and the release of lactate dehydrogenase of tumor cells are observed after the treatment of VTPA, resulting in a specific pyroptotic cell death. To our best knowledge, the structure-dependent and tumor intracellular GSH activatable pyroptotic agents represent the first demonstration of cancer-specific pyroptosis in vivo, providing a novel paradigm for the development of next-generation cancer-specific pyroptotic nanomedicine.
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