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Canady Cold Helios Plasma Reduces Soft Tissue Sarcoma Viability by Inhibiting Proliferation, Disrupting Cell Cycle, and Inducing Apoptosis: A Preliminary Report
Soft tissue sarcomas (STS) are a rare and highly heterogeneous group of solid tumors, originating from various types of connective tissue. Complete removal of STS by surgery is challenging due to the anatomical location of the tumor, which results in tumor recurrence. Additionally, current polychemo...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268132/ https://www.ncbi.nlm.nih.gov/pubmed/35807413 http://dx.doi.org/10.3390/molecules27134168 |
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author | Ly, Lawan Cheng, Xiaoqian Murthy, Saravana R. K. Jones, Olivia Z. Zhuang, Taisen Gitelis, Steven Blank, Alan T. Nissan, Aviram Adileh, Mohammad Colman, Matthew Keidar, Michael Basadonna, Giacomo Canady, Jerome |
author_facet | Ly, Lawan Cheng, Xiaoqian Murthy, Saravana R. K. Jones, Olivia Z. Zhuang, Taisen Gitelis, Steven Blank, Alan T. Nissan, Aviram Adileh, Mohammad Colman, Matthew Keidar, Michael Basadonna, Giacomo Canady, Jerome |
author_sort | Ly, Lawan |
collection | PubMed |
description | Soft tissue sarcomas (STS) are a rare and highly heterogeneous group of solid tumors, originating from various types of connective tissue. Complete removal of STS by surgery is challenging due to the anatomical location of the tumor, which results in tumor recurrence. Additionally, current polychemotherapeutic regimens are highly toxic with no rational survival benefit. Cold atmospheric plasma (CAP) is a novel technology that has demonstrated immense cancer therapeutic potential. Canady Cold Helios Plasma (CHCP) is a device that sprays CAP along the surgical margins to eradicate residual cancer cells after tumor resection. This preliminary study was conducted in vitro prior to in vivo testing in a humanitarian compassionate use case study and an FDA-approved phase 1 clinical trial (IDE G190165). In this study, the authors evaluate the efficacy of CHCP across multiple STS cell lines. CHCP treatment reduced the viability of four different STS cell lines (i.e., fibrosarcoma, synovial sarcoma, rhabdomyosarcoma, and liposarcoma) in a dose-dependent manner by inhibiting proliferation, disrupting cell cycle, and inducing apoptosis-like cell death. |
format | Online Article Text |
id | pubmed-9268132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92681322022-07-09 Canady Cold Helios Plasma Reduces Soft Tissue Sarcoma Viability by Inhibiting Proliferation, Disrupting Cell Cycle, and Inducing Apoptosis: A Preliminary Report Ly, Lawan Cheng, Xiaoqian Murthy, Saravana R. K. Jones, Olivia Z. Zhuang, Taisen Gitelis, Steven Blank, Alan T. Nissan, Aviram Adileh, Mohammad Colman, Matthew Keidar, Michael Basadonna, Giacomo Canady, Jerome Molecules Article Soft tissue sarcomas (STS) are a rare and highly heterogeneous group of solid tumors, originating from various types of connective tissue. Complete removal of STS by surgery is challenging due to the anatomical location of the tumor, which results in tumor recurrence. Additionally, current polychemotherapeutic regimens are highly toxic with no rational survival benefit. Cold atmospheric plasma (CAP) is a novel technology that has demonstrated immense cancer therapeutic potential. Canady Cold Helios Plasma (CHCP) is a device that sprays CAP along the surgical margins to eradicate residual cancer cells after tumor resection. This preliminary study was conducted in vitro prior to in vivo testing in a humanitarian compassionate use case study and an FDA-approved phase 1 clinical trial (IDE G190165). In this study, the authors evaluate the efficacy of CHCP across multiple STS cell lines. CHCP treatment reduced the viability of four different STS cell lines (i.e., fibrosarcoma, synovial sarcoma, rhabdomyosarcoma, and liposarcoma) in a dose-dependent manner by inhibiting proliferation, disrupting cell cycle, and inducing apoptosis-like cell death. MDPI 2022-06-29 /pmc/articles/PMC9268132/ /pubmed/35807413 http://dx.doi.org/10.3390/molecules27134168 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ly, Lawan Cheng, Xiaoqian Murthy, Saravana R. K. Jones, Olivia Z. Zhuang, Taisen Gitelis, Steven Blank, Alan T. Nissan, Aviram Adileh, Mohammad Colman, Matthew Keidar, Michael Basadonna, Giacomo Canady, Jerome Canady Cold Helios Plasma Reduces Soft Tissue Sarcoma Viability by Inhibiting Proliferation, Disrupting Cell Cycle, and Inducing Apoptosis: A Preliminary Report |
title | Canady Cold Helios Plasma Reduces Soft Tissue Sarcoma Viability by Inhibiting Proliferation, Disrupting Cell Cycle, and Inducing Apoptosis: A Preliminary Report |
title_full | Canady Cold Helios Plasma Reduces Soft Tissue Sarcoma Viability by Inhibiting Proliferation, Disrupting Cell Cycle, and Inducing Apoptosis: A Preliminary Report |
title_fullStr | Canady Cold Helios Plasma Reduces Soft Tissue Sarcoma Viability by Inhibiting Proliferation, Disrupting Cell Cycle, and Inducing Apoptosis: A Preliminary Report |
title_full_unstemmed | Canady Cold Helios Plasma Reduces Soft Tissue Sarcoma Viability by Inhibiting Proliferation, Disrupting Cell Cycle, and Inducing Apoptosis: A Preliminary Report |
title_short | Canady Cold Helios Plasma Reduces Soft Tissue Sarcoma Viability by Inhibiting Proliferation, Disrupting Cell Cycle, and Inducing Apoptosis: A Preliminary Report |
title_sort | canady cold helios plasma reduces soft tissue sarcoma viability by inhibiting proliferation, disrupting cell cycle, and inducing apoptosis: a preliminary report |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268132/ https://www.ncbi.nlm.nih.gov/pubmed/35807413 http://dx.doi.org/10.3390/molecules27134168 |
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