A Virus‐Spike Tumor‐Activatable Pyroptotic Agent. Issue 8 (1st February 2021)

• Record Type: Journal Article
• Authors: Nadeem, Sadia; Yang, Chuang; Du, Yang; Li, Fangyuan; Chen, Zheng; Zhou, Yan; Lee, Ji Young; Ding, Qiang; Ling, Daishun
• Is Part Of: Small. Volume 17:Issue 8(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-02-01
• Subjects: cancer therapy -- nanostructures -- pyroptosis -- spiky surface -- tumor‐activatable pyroptotic agents; Nanotechnology -- Periodicals; Nanoparticles -- Periodicals; Microtechnology -- Periodicals; 620.5
• DOI: 10.1002/smll.202006599
• Languages: English
• ISSNs: 1613-6810

Abstract

Abstract: 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. Abstract : A virus‐spike tumor‐activatable pyroptotic agent is developed for dual lysosomal rupture/reactive oxygen species (ROS) generation based tumor pyroptosis. The spiky manganese dioxide protrusions are decorated on the surface of organosilica to facilitate the intracellular lysosomal rupture. Subsequently, the manganese dioxide protrusions degrade in response to the glutathione and elicit Fenton‐like reaction for ROS generation that synergistically activates the inflammasomes.