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The effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model
Melanoma remains a deadly cancer despite significant advances in immune checkpoint blockade and targeted therapies. The incidence of melanoma is also growing worldwide, which highlights the need for novel treatment options and strategic combination of therapies. Here, we investigate non‐thermal plas...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472020/ https://www.ncbi.nlm.nih.gov/pubmed/36176603 http://dx.doi.org/10.1002/btm2.10314 |
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author | Lin, Abraham De Backer, Joey Quatannens, Delphine Cuypers, Bart Verswyvel, Hanne De La Hoz, Edgar Cardenas Ribbens, Bart Siozopoulou, Vasiliki Van Audenaerde, Jonas Marcq, Elly Lardon, Filip Laukens, Kris Vanlanduit, Steve Smits, Evelien Bogaerts, Annemie |
author_facet | Lin, Abraham De Backer, Joey Quatannens, Delphine Cuypers, Bart Verswyvel, Hanne De La Hoz, Edgar Cardenas Ribbens, Bart Siozopoulou, Vasiliki Van Audenaerde, Jonas Marcq, Elly Lardon, Filip Laukens, Kris Vanlanduit, Steve Smits, Evelien Bogaerts, Annemie |
author_sort | Lin, Abraham |
collection | PubMed |
description | Melanoma remains a deadly cancer despite significant advances in immune checkpoint blockade and targeted therapies. The incidence of melanoma is also growing worldwide, which highlights the need for novel treatment options and strategic combination of therapies. Here, we investigate non‐thermal plasma (NTP), an ionized gas, as a promising, therapeutic option. In a melanoma mouse model, direct treatment of tumors with NTP results in reduced tumor burden and prolonged survival. Physical characterization of NTP treatment in situ reveals the deposited NTP energy and temperature associated with therapy response, and whole transcriptome analysis of the tumor identified several modulated pathways. NTP treatment also enhances the cancer‐immunity cycle, as immune cells in both the tumor and tumor‐draining lymph nodes appear more stimulated to perform their anti‐cancer functions. Thus, our data suggest that local NTP therapy stimulates systemic, anti‐cancer immunity. We discuss, in detail, how these fundamental insights will help direct the translation of NTP technology into the clinic and inform rational combination strategies to address the challenges in melanoma therapy. |
format | Online Article Text |
id | pubmed-9472020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94720202022-09-28 The effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model Lin, Abraham De Backer, Joey Quatannens, Delphine Cuypers, Bart Verswyvel, Hanne De La Hoz, Edgar Cardenas Ribbens, Bart Siozopoulou, Vasiliki Van Audenaerde, Jonas Marcq, Elly Lardon, Filip Laukens, Kris Vanlanduit, Steve Smits, Evelien Bogaerts, Annemie Bioeng Transl Med Research Articles Melanoma remains a deadly cancer despite significant advances in immune checkpoint blockade and targeted therapies. The incidence of melanoma is also growing worldwide, which highlights the need for novel treatment options and strategic combination of therapies. Here, we investigate non‐thermal plasma (NTP), an ionized gas, as a promising, therapeutic option. In a melanoma mouse model, direct treatment of tumors with NTP results in reduced tumor burden and prolonged survival. Physical characterization of NTP treatment in situ reveals the deposited NTP energy and temperature associated with therapy response, and whole transcriptome analysis of the tumor identified several modulated pathways. NTP treatment also enhances the cancer‐immunity cycle, as immune cells in both the tumor and tumor‐draining lymph nodes appear more stimulated to perform their anti‐cancer functions. Thus, our data suggest that local NTP therapy stimulates systemic, anti‐cancer immunity. We discuss, in detail, how these fundamental insights will help direct the translation of NTP technology into the clinic and inform rational combination strategies to address the challenges in melanoma therapy. John Wiley & Sons, Inc. 2022-04-21 /pmc/articles/PMC9472020/ /pubmed/36176603 http://dx.doi.org/10.1002/btm2.10314 Text en © 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Lin, Abraham De Backer, Joey Quatannens, Delphine Cuypers, Bart Verswyvel, Hanne De La Hoz, Edgar Cardenas Ribbens, Bart Siozopoulou, Vasiliki Van Audenaerde, Jonas Marcq, Elly Lardon, Filip Laukens, Kris Vanlanduit, Steve Smits, Evelien Bogaerts, Annemie The effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model |
title | The effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model |
title_full | The effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model |
title_fullStr | The effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model |
title_full_unstemmed | The effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model |
title_short | The effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model |
title_sort | effect of local non‐thermal plasma therapy on the cancer‐immunity cycle in a melanoma mouse model |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472020/ https://www.ncbi.nlm.nih.gov/pubmed/36176603 http://dx.doi.org/10.1002/btm2.10314 |
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