Necroptosis-Inducible Polymeric Nanobubbles for Enhanced Cancer Sonoimmunotherapy

© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 32(2020), 16 vom: 12. Apr., Seite e1907953
1. Verfasser: Um, Wooram (VerfasserIn)
Weitere Verfasser: Ko, Hyewon, You, Dong Gil, Lim, Seungho, Kwak, Gijung, Shim, Man Kyu, Yang, Suah, Lee, Jeongjin, Song, Yeari, Kim, Kwangmeyung, Park, Jae Hyung
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article damage-associated molecular patterns immune checkpoint blockade necroptosis reactive oxygen species sonodynamic therapy Polymers
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520 |a Necroptosis, caspase-independent programmed necrosis, has emerged as a therapeutic target to make dying cancer cells stimulants for antitumor immune responses. The clinical translations exploiting necroptosis, however, have been limited since most cancer cells downregulate receptor-interacting protein kinase 3 (RIPK3) as a key enzyme for necroptosis. Herein, nanobubbles (NBs) that can trigger RIPK3-independent necroptosis, facilitating cell-membrane rupture via the acoustic cavitation effect are reported. The NBs, imbibing perfluoropentane as the gas precursor, are prepared using an amphiphilic polymer conjugate, composed of PEGylated carboxymethyl dextran as the hydrophilic backbone and chlorin e6 as the hydrophobic sonosensitizer. When exposed to ultrasound, the NBs efficiently promote the release of biologically active damage-associated molecular patterns by inducing burst-mediated cell-membrane disintegration. Consequently, the necroptosis-inducible NBs significantly improve antitumor immunity by maturation of dendritic cells and activation of CD8+ cytotoxic T cells both in vitro and in vivo. In addition, the combination of NBs and immune checkpoint blockade leads to complete regression of the primary tumor and beneficial therapeutic activity against metastatic tumors in an RIPK3-deficient CT26 tumor-bearing mouse model. Overall, the innovative NB that causes immunogenic cell death of cancer via RIPK3-independent necroptosis is a promising enhancer for cancer immunotherapy 
650 4 |a Journal Article 
650 4 |a damage-associated molecular patterns 
650 4 |a immune checkpoint blockade 
650 4 |a necroptosis 
650 4 |a reactive oxygen species 
650 4 |a sonodynamic therapy 
650 7 |a Polymers  |2 NLM 
700 1 |a Ko, Hyewon  |e verfasserin  |4 aut 
700 1 |a You, Dong Gil  |e verfasserin  |4 aut 
700 1 |a Lim, Seungho  |e verfasserin  |4 aut 
700 1 |a Kwak, Gijung  |e verfasserin  |4 aut 
700 1 |a Shim, Man Kyu  |e verfasserin  |4 aut 
700 1 |a Yang, Suah  |e verfasserin  |4 aut 
700 1 |a Lee, Jeongjin  |e verfasserin  |4 aut 
700 1 |a Song, Yeari  |e verfasserin  |4 aut 
700 1 |a Kim, Kwangmeyung  |e verfasserin  |4 aut 
700 1 |a Park, Jae Hyung  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Advanced materials (Deerfield Beach, Fla.)  |d 1998  |g 32(2020), 16 vom: 12. Apr., Seite e1907953  |w (DE-627)NLM098206397  |x 1521-4095  |7 nnns 
773 1 8 |g volume:32  |g year:2020  |g number:16  |g day:12  |g month:04  |g pages:e1907953 
856 4 0 |u http://dx.doi.org/10.1002/adma.201907953  |3 Volltext 
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