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The effect of local non-thermal plasma therapy on the cancer-immunity cycle in a melanoma mouse model.

Authors :
Lin A
De Backer J
Quatannens D
Cuypers B
Verswyvel H
De La Hoz EC
Ribbens B
Siozopoulou V
Van Audenaerde J
Marcq E
Lardon F
Laukens K
Vanlanduit S
Smits E
Bogaerts A
Source :
Bioengineering & translational medicine [Bioeng Transl Med] 2022 Apr 21; Vol. 7 (3), pp. e10314. Date of Electronic Publication: 2022 Apr 21 (Print Publication: 2022).
Publication Year :
2022

Abstract

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.<br /> (© 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers.)

Details

Language :
English
ISSN :
2380-6761
Volume :
7
Issue :
3
Database :
MEDLINE
Journal :
Bioengineering & translational medicine
Publication Type :
Academic Journal
Accession number :
36176603
Full Text :
https://doi.org/10.1002/btm2.10314