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Combination of Irreversible Electroporation and STING Agonist for Effective Cancer Immunotherapy

SIMPLE SUMMARY: This study deals with a new strategy for effective cancer immunotherapy using a combination of electrical ablation and immune adjuvant, a stimulator of interferon genes (STING) agonist. The combination treatment significantly improved the cancer treatment effect by converting the imm...

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Autores principales: Go, Eun-Jin, Yang, Hannah, Chon, Hong Jae, Yang, DaSom, Ryu, WonHyoung, Kim, Dong-Hyun, Han, Dong Keun, Kim, Chan, Park, Wooram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693597/
https://www.ncbi.nlm.nih.gov/pubmed/33114476
http://dx.doi.org/10.3390/cancers12113123
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author Go, Eun-Jin
Yang, Hannah
Chon, Hong Jae
Yang, DaSom
Ryu, WonHyoung
Kim, Dong-Hyun
Han, Dong Keun
Kim, Chan
Park, Wooram
author_facet Go, Eun-Jin
Yang, Hannah
Chon, Hong Jae
Yang, DaSom
Ryu, WonHyoung
Kim, Dong-Hyun
Han, Dong Keun
Kim, Chan
Park, Wooram
author_sort Go, Eun-Jin
collection PubMed
description SIMPLE SUMMARY: This study deals with a new strategy for effective cancer immunotherapy using a combination of electrical ablation and immune adjuvant, a stimulator of interferon genes (STING) agonist. The combination treatment significantly improved the cancer treatment effect by converting the immunosuppressive tumor microenvironment (TME) to an immunogenic TME. The combination of interventional oncology and immuno-oncology is expected to contribute to the treatment of various difficult-to-treat tumors. ABSTRACT: Recently, cancer immunotherapy has received attention as a viable solution for the treatment of refractory tumors. However, it still has clinical limitations in its treatment efficacy due to inter-patient tumor heterogeneity and immunosuppressive tumor microenvironment (TME). In this study, we demonstrated the triggering of anti-cancer immune responses by a combination of irreversible electroporation (IRE) and a stimulator of interferon genes (STING) agonist. Optimal electrical conditions inducing damage-associated molecular patterns (DAMPs) by immunogenic cell death (ICD) were determined through in vitro 2D and 3D cell experiments. In the in vivo syngeneic lung cancer model, the combination of IRE and STING agonists demonstrated significant tumor growth inhibition. We believe that the combination strategy of IRE and STING agonists has potential for effective cancer immunotherapy.
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spelling pubmed-76935972020-11-28 Combination of Irreversible Electroporation and STING Agonist for Effective Cancer Immunotherapy Go, Eun-Jin Yang, Hannah Chon, Hong Jae Yang, DaSom Ryu, WonHyoung Kim, Dong-Hyun Han, Dong Keun Kim, Chan Park, Wooram Cancers (Basel) Article SIMPLE SUMMARY: This study deals with a new strategy for effective cancer immunotherapy using a combination of electrical ablation and immune adjuvant, a stimulator of interferon genes (STING) agonist. The combination treatment significantly improved the cancer treatment effect by converting the immunosuppressive tumor microenvironment (TME) to an immunogenic TME. The combination of interventional oncology and immuno-oncology is expected to contribute to the treatment of various difficult-to-treat tumors. ABSTRACT: Recently, cancer immunotherapy has received attention as a viable solution for the treatment of refractory tumors. However, it still has clinical limitations in its treatment efficacy due to inter-patient tumor heterogeneity and immunosuppressive tumor microenvironment (TME). In this study, we demonstrated the triggering of anti-cancer immune responses by a combination of irreversible electroporation (IRE) and a stimulator of interferon genes (STING) agonist. Optimal electrical conditions inducing damage-associated molecular patterns (DAMPs) by immunogenic cell death (ICD) were determined through in vitro 2D and 3D cell experiments. In the in vivo syngeneic lung cancer model, the combination of IRE and STING agonists demonstrated significant tumor growth inhibition. We believe that the combination strategy of IRE and STING agonists has potential for effective cancer immunotherapy. MDPI 2020-10-26 /pmc/articles/PMC7693597/ /pubmed/33114476 http://dx.doi.org/10.3390/cancers12113123 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Go, Eun-Jin
Yang, Hannah
Chon, Hong Jae
Yang, DaSom
Ryu, WonHyoung
Kim, Dong-Hyun
Han, Dong Keun
Kim, Chan
Park, Wooram
Combination of Irreversible Electroporation and STING Agonist for Effective Cancer Immunotherapy
title Combination of Irreversible Electroporation and STING Agonist for Effective Cancer Immunotherapy
title_full Combination of Irreversible Electroporation and STING Agonist for Effective Cancer Immunotherapy
title_fullStr Combination of Irreversible Electroporation and STING Agonist for Effective Cancer Immunotherapy
title_full_unstemmed Combination of Irreversible Electroporation and STING Agonist for Effective Cancer Immunotherapy
title_short Combination of Irreversible Electroporation and STING Agonist for Effective Cancer Immunotherapy
title_sort combination of irreversible electroporation and sting agonist for effective cancer immunotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693597/
https://www.ncbi.nlm.nih.gov/pubmed/33114476
http://dx.doi.org/10.3390/cancers12113123
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