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Nano-pulse stimulation™ therapy (NPS™) is superior to cryoablation in clearing murine melanoma tumors

BACKGROUND: Nano-Pulse Stimulation™ Therapy (NPS™) is a new, bioelectric modality that applies ultrashort pulses of electric energy to trigger regulated cell death in treated tissues. Instead of initiating necrosis by heating or freezing, NPS therapy permeabilizes intracellular organelles to activat...

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Autores principales: McDaniel, Amanda, Freimark, Bruce, Navarro, Cebrina, Von Rothstein, Kristin, Gonzalez, Dacia, Linder, Keith, Nuccitelli, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945337/
https://www.ncbi.nlm.nih.gov/pubmed/36844920
http://dx.doi.org/10.3389/fonc.2022.948472
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author McDaniel, Amanda
Freimark, Bruce
Navarro, Cebrina
Von Rothstein, Kristin
Gonzalez, Dacia
Linder, Keith
Nuccitelli, Richard
author_facet McDaniel, Amanda
Freimark, Bruce
Navarro, Cebrina
Von Rothstein, Kristin
Gonzalez, Dacia
Linder, Keith
Nuccitelli, Richard
author_sort McDaniel, Amanda
collection PubMed
description BACKGROUND: Nano-Pulse Stimulation™ Therapy (NPS™) is a new, bioelectric modality that applies ultrashort pulses of electric energy to trigger regulated cell death in treated tissues. Instead of initiating necrosis by heating or freezing, NPS therapy permeabilizes intracellular organelles to activate the cell’s own self-destruct pathway of programmed or regulated cell death. Unlike cryotherapies that can both damage structural tissues and diffuse into the periphery beyond the margins of the lesion, NPS only affects cells within the treated zone leaving surrounding tissue and acellular components unaffected. METHODS: We generated melanoma tumors in mice by injecting B16-F10 cells intradermally and compared the efficacy and resulting skin damage from Nano-Pulse Stimulation Therapy with that of cryoablation in clearing these tumors. RESULTS: The results of the study demonstrate that NPS is superior at clearing B16-F10 melanoma lesions. NPS permanently eliminated up to 91% of all tumor lesions with a single treatment compared to cryoablation that only eliminated up to 66%. Importantly, NPS permanently eliminated these lesions with no recurrence and with minimal dermal fibrosis, underlying muscle atrophy, permanent hair follicle loss or other markers of permanent skin damage. CONCLUSIONS: These findings suggest that NPS is a promising new modality for the clearance of melanoma tumors and is a more efficacious, less damaging approach than cryoablative methods for the treatment of aggressive malignant tumors.
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spelling pubmed-99453372023-02-23 Nano-pulse stimulation™ therapy (NPS™) is superior to cryoablation in clearing murine melanoma tumors McDaniel, Amanda Freimark, Bruce Navarro, Cebrina Von Rothstein, Kristin Gonzalez, Dacia Linder, Keith Nuccitelli, Richard Front Oncol Oncology BACKGROUND: Nano-Pulse Stimulation™ Therapy (NPS™) is a new, bioelectric modality that applies ultrashort pulses of electric energy to trigger regulated cell death in treated tissues. Instead of initiating necrosis by heating or freezing, NPS therapy permeabilizes intracellular organelles to activate the cell’s own self-destruct pathway of programmed or regulated cell death. Unlike cryotherapies that can both damage structural tissues and diffuse into the periphery beyond the margins of the lesion, NPS only affects cells within the treated zone leaving surrounding tissue and acellular components unaffected. METHODS: We generated melanoma tumors in mice by injecting B16-F10 cells intradermally and compared the efficacy and resulting skin damage from Nano-Pulse Stimulation Therapy with that of cryoablation in clearing these tumors. RESULTS: The results of the study demonstrate that NPS is superior at clearing B16-F10 melanoma lesions. NPS permanently eliminated up to 91% of all tumor lesions with a single treatment compared to cryoablation that only eliminated up to 66%. Importantly, NPS permanently eliminated these lesions with no recurrence and with minimal dermal fibrosis, underlying muscle atrophy, permanent hair follicle loss or other markers of permanent skin damage. CONCLUSIONS: These findings suggest that NPS is a promising new modality for the clearance of melanoma tumors and is a more efficacious, less damaging approach than cryoablative methods for the treatment of aggressive malignant tumors. Frontiers Media S.A. 2023-02-08 /pmc/articles/PMC9945337/ /pubmed/36844920 http://dx.doi.org/10.3389/fonc.2022.948472 Text en Copyright © 2023 McDaniel, Freimark, Navarro, Von Rothstein, Gonzalez, Linder and Nuccitelli https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
McDaniel, Amanda
Freimark, Bruce
Navarro, Cebrina
Von Rothstein, Kristin
Gonzalez, Dacia
Linder, Keith
Nuccitelli, Richard
Nano-pulse stimulation™ therapy (NPS™) is superior to cryoablation in clearing murine melanoma tumors
title Nano-pulse stimulation™ therapy (NPS™) is superior to cryoablation in clearing murine melanoma tumors
title_full Nano-pulse stimulation™ therapy (NPS™) is superior to cryoablation in clearing murine melanoma tumors
title_fullStr Nano-pulse stimulation™ therapy (NPS™) is superior to cryoablation in clearing murine melanoma tumors
title_full_unstemmed Nano-pulse stimulation™ therapy (NPS™) is superior to cryoablation in clearing murine melanoma tumors
title_short Nano-pulse stimulation™ therapy (NPS™) is superior to cryoablation in clearing murine melanoma tumors
title_sort nano-pulse stimulation™ therapy (nps™) is superior to cryoablation in clearing murine melanoma tumors
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945337/
https://www.ncbi.nlm.nih.gov/pubmed/36844920
http://dx.doi.org/10.3389/fonc.2022.948472
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