Cargando…

Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering

Intractable cancers such as osteosarcoma (OS) and oral cancer (OC) are highly refractory, recurrent, and metastatic once developed, and their prognosis is still disappointing. Tumor-targeted therapy, which eliminates cancers effectively and safely, is the current clinical choice. Since aggressive tu...

Descripción completa

Detalles Bibliográficos
Autores principales: Suzuki-Karasaki, Manami, Ando, Takashi, Ochiai, Yushi, Kawahara, Kenta, Suzuki-Karasaki, Miki, Nakayama, Hideki, Suzuki-Karasaki, Yoshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835529/
https://www.ncbi.nlm.nih.gov/pubmed/35163042
http://dx.doi.org/10.3390/ijms23031124
_version_ 1784649456278306816
author Suzuki-Karasaki, Manami
Ando, Takashi
Ochiai, Yushi
Kawahara, Kenta
Suzuki-Karasaki, Miki
Nakayama, Hideki
Suzuki-Karasaki, Yoshihiro
author_facet Suzuki-Karasaki, Manami
Ando, Takashi
Ochiai, Yushi
Kawahara, Kenta
Suzuki-Karasaki, Miki
Nakayama, Hideki
Suzuki-Karasaki, Yoshihiro
author_sort Suzuki-Karasaki, Manami
collection PubMed
description Intractable cancers such as osteosarcoma (OS) and oral cancer (OC) are highly refractory, recurrent, and metastatic once developed, and their prognosis is still disappointing. Tumor-targeted therapy, which eliminates cancers effectively and safely, is the current clinical choice. Since aggressive tumors are substantially resistant to multidisciplinary therapies that target apoptosis, tumor-specific activation of another cell death modality is a promising avenue for meeting this goal. Here, we report that a cold atmospheric air plasma-activated medium (APAM) can kill OS and OC by causing a unique mitochondrial clustering. This event was named monopolar perinuclear mitochondrial clustering (MPMC) based on its characteristic unipolar mitochondrial perinuclear accumulation. The APAM caused apoptotic and nonapoptotic cell death. The APAM increased mitochondrial ROS (mROS) and cell death, and the antioxidants such as N-acetylcysteine (NAC) prevented them. MPMC occurred following mitochondrial fragmentation, which coincided with nuclear damages. MPMC was accompanied by mitochondrial lipid peroxide (mLPO) accumulation and prevented by NAC, Ferrostatin-1, and Nocodazole. In contrast, the APAM induced minimal cell death, mROS generation, mLPO accumulation, and MPMC in fibroblasts. These results suggest that MPMC occurs in a tumor-specific manner via mitochondrial oxidative stress and microtubule-driven mitochondrial motility. MPMC induction might serve as a promising target for exerting tumor-specific cytotoxicity.
format Online
Article
Text
id pubmed-8835529
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-88355292022-02-12 Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering Suzuki-Karasaki, Manami Ando, Takashi Ochiai, Yushi Kawahara, Kenta Suzuki-Karasaki, Miki Nakayama, Hideki Suzuki-Karasaki, Yoshihiro Int J Mol Sci Article Intractable cancers such as osteosarcoma (OS) and oral cancer (OC) are highly refractory, recurrent, and metastatic once developed, and their prognosis is still disappointing. Tumor-targeted therapy, which eliminates cancers effectively and safely, is the current clinical choice. Since aggressive tumors are substantially resistant to multidisciplinary therapies that target apoptosis, tumor-specific activation of another cell death modality is a promising avenue for meeting this goal. Here, we report that a cold atmospheric air plasma-activated medium (APAM) can kill OS and OC by causing a unique mitochondrial clustering. This event was named monopolar perinuclear mitochondrial clustering (MPMC) based on its characteristic unipolar mitochondrial perinuclear accumulation. The APAM caused apoptotic and nonapoptotic cell death. The APAM increased mitochondrial ROS (mROS) and cell death, and the antioxidants such as N-acetylcysteine (NAC) prevented them. MPMC occurred following mitochondrial fragmentation, which coincided with nuclear damages. MPMC was accompanied by mitochondrial lipid peroxide (mLPO) accumulation and prevented by NAC, Ferrostatin-1, and Nocodazole. In contrast, the APAM induced minimal cell death, mROS generation, mLPO accumulation, and MPMC in fibroblasts. These results suggest that MPMC occurs in a tumor-specific manner via mitochondrial oxidative stress and microtubule-driven mitochondrial motility. MPMC induction might serve as a promising target for exerting tumor-specific cytotoxicity. MDPI 2022-01-20 /pmc/articles/PMC8835529/ /pubmed/35163042 http://dx.doi.org/10.3390/ijms23031124 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
Suzuki-Karasaki, Manami
Ando, Takashi
Ochiai, Yushi
Kawahara, Kenta
Suzuki-Karasaki, Miki
Nakayama, Hideki
Suzuki-Karasaki, Yoshihiro
Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering
title Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering
title_full Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering
title_fullStr Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering
title_full_unstemmed Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering
title_short Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering
title_sort air plasma-activated medium evokes a death-associated perinuclear mitochondrial clustering
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835529/
https://www.ncbi.nlm.nih.gov/pubmed/35163042
http://dx.doi.org/10.3390/ijms23031124
work_keys_str_mv AT suzukikarasakimanami airplasmaactivatedmediumevokesadeathassociatedperinuclearmitochondrialclustering
AT andotakashi airplasmaactivatedmediumevokesadeathassociatedperinuclearmitochondrialclustering
AT ochiaiyushi airplasmaactivatedmediumevokesadeathassociatedperinuclearmitochondrialclustering
AT kawaharakenta airplasmaactivatedmediumevokesadeathassociatedperinuclearmitochondrialclustering
AT suzukikarasakimiki airplasmaactivatedmediumevokesadeathassociatedperinuclearmitochondrialclustering
AT nakayamahideki airplasmaactivatedmediumevokesadeathassociatedperinuclearmitochondrialclustering
AT suzukikarasakiyoshihiro airplasmaactivatedmediumevokesadeathassociatedperinuclearmitochondrialclustering