Cargando…

Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses

Radiofrequency ablation (RFA) is clinically adopted to destruct solid tumors, but is often incapable of completely ablating large tumors and those with multiple metastatic sites. Here we develop a CaCO(3)-assisted double emulsion method to encapsulate lipoxidase and hemin with poly(lactic-co-glycoli...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Zhijuan, Zhu, Yujie, Dong, Ziliang, Li, Wei, Yang, Nailin, Wang, Xianwen, Feng, Liangzhu, Liu, Zhuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280226/
https://www.ncbi.nlm.nih.gov/pubmed/34262038
http://dx.doi.org/10.1038/s41467-021-24604-9
_version_ 1783722608156475392
author Yang, Zhijuan
Zhu, Yujie
Dong, Ziliang
Li, Wei
Yang, Nailin
Wang, Xianwen
Feng, Liangzhu
Liu, Zhuang
author_facet Yang, Zhijuan
Zhu, Yujie
Dong, Ziliang
Li, Wei
Yang, Nailin
Wang, Xianwen
Feng, Liangzhu
Liu, Zhuang
author_sort Yang, Zhijuan
collection PubMed
description Radiofrequency ablation (RFA) is clinically adopted to destruct solid tumors, but is often incapable of completely ablating large tumors and those with multiple metastatic sites. Here we develop a CaCO(3)-assisted double emulsion method to encapsulate lipoxidase and hemin with poly(lactic-co-glycolic acid) (PLGA) to enhance RFA. We show the HLCaP nanoreactors (NRs) with pH-dependent catalytic capacity can continuously produce cytotoxic lipid radicals via the lipid peroxidation chain reaction using cancer cell debris as the fuel. Upon being fixed inside the residual tumors post RFA, HLCaP NRs exhibit a suppression effect on residual tumors in mice and rabbits by triggering ferroptosis. Moreover, treatment with HLCaP NRs post RFA can prime antitumor immunity to effectively suppress the growth of both residual and metastatic tumors, also in combination with immune checkpoint blockade. This work highlights that tumor-debris-fueled nanoreactors can benefit RFA by inhibiting tumor recurrence and preventing tumor metastasis.
format Online
Article
Text
id pubmed-8280226
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-82802262021-07-23 Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses Yang, Zhijuan Zhu, Yujie Dong, Ziliang Li, Wei Yang, Nailin Wang, Xianwen Feng, Liangzhu Liu, Zhuang Nat Commun Article Radiofrequency ablation (RFA) is clinically adopted to destruct solid tumors, but is often incapable of completely ablating large tumors and those with multiple metastatic sites. Here we develop a CaCO(3)-assisted double emulsion method to encapsulate lipoxidase and hemin with poly(lactic-co-glycolic acid) (PLGA) to enhance RFA. We show the HLCaP nanoreactors (NRs) with pH-dependent catalytic capacity can continuously produce cytotoxic lipid radicals via the lipid peroxidation chain reaction using cancer cell debris as the fuel. Upon being fixed inside the residual tumors post RFA, HLCaP NRs exhibit a suppression effect on residual tumors in mice and rabbits by triggering ferroptosis. Moreover, treatment with HLCaP NRs post RFA can prime antitumor immunity to effectively suppress the growth of both residual and metastatic tumors, also in combination with immune checkpoint blockade. This work highlights that tumor-debris-fueled nanoreactors can benefit RFA by inhibiting tumor recurrence and preventing tumor metastasis. Nature Publishing Group UK 2021-07-14 /pmc/articles/PMC8280226/ /pubmed/34262038 http://dx.doi.org/10.1038/s41467-021-24604-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yang, Zhijuan
Zhu, Yujie
Dong, Ziliang
Li, Wei
Yang, Nailin
Wang, Xianwen
Feng, Liangzhu
Liu, Zhuang
Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses
title Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses
title_full Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses
title_fullStr Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses
title_full_unstemmed Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses
title_short Tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses
title_sort tumor-killing nanoreactors fueled by tumor debris can enhance radiofrequency ablation therapy and boost antitumor immune responses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8280226/
https://www.ncbi.nlm.nih.gov/pubmed/34262038
http://dx.doi.org/10.1038/s41467-021-24604-9
work_keys_str_mv AT yangzhijuan tumorkillingnanoreactorsfueledbytumordebriscanenhanceradiofrequencyablationtherapyandboostantitumorimmuneresponses
AT zhuyujie tumorkillingnanoreactorsfueledbytumordebriscanenhanceradiofrequencyablationtherapyandboostantitumorimmuneresponses
AT dongziliang tumorkillingnanoreactorsfueledbytumordebriscanenhanceradiofrequencyablationtherapyandboostantitumorimmuneresponses
AT liwei tumorkillingnanoreactorsfueledbytumordebriscanenhanceradiofrequencyablationtherapyandboostantitumorimmuneresponses
AT yangnailin tumorkillingnanoreactorsfueledbytumordebriscanenhanceradiofrequencyablationtherapyandboostantitumorimmuneresponses
AT wangxianwen tumorkillingnanoreactorsfueledbytumordebriscanenhanceradiofrequencyablationtherapyandboostantitumorimmuneresponses
AT fengliangzhu tumorkillingnanoreactorsfueledbytumordebriscanenhanceradiofrequencyablationtherapyandboostantitumorimmuneresponses
AT liuzhuang tumorkillingnanoreactorsfueledbytumordebriscanenhanceradiofrequencyablationtherapyandboostantitumorimmuneresponses