Sevoflurane modulates the cancer stem cell-like properties and mitochondrial membrane potential of glioma via Ca


Journal

Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521

Informations de publication

Date de publication:
15 Jul 2020
Historique:
received: 21 01 2020
revised: 01 04 2020
accepted: 11 04 2020
pubmed: 4 5 2020
medline: 17 6 2020
entrez: 4 5 2020
Statut: ppublish

Résumé

Gliomas are responsible for the majority of deaths from primary brain tumours. Sevoflurane showed inhibition effects on the tumor progression in vitro. However, whether sevoflurane could affect the stemness of glioma stem cells (GSCs) and the potential molecular mechanism have not been well elucidated. Effects of sevoflurane on cell viability, proliferation and invasion ability of glioma cells as well as tumor growth in vivo were assessed. Sphere formation assay was performed to evaluate the effect of sevoflurane on the stemness of GSCs. Effects of sevoflurane on mitochondrial function was evaluated by intracellular/mitochondrial reactive oxygen species (ROS) level and mitochondrial membrane potential. Expression levels of proliferation-related proteins, stemness markers and proteins in CaMKII/JNK cascade were measured by Western blot. Sevoflurane inhibited the viability, proliferation and invasion ability of glioma cells (U87MG and U373MG). Western blot showed that sevoflurane decreased the expression levels of proliferation and invasion-related proteins. Sphere formation ability of GSCs, expression levels of stemness markers and mitochondrial function were significantly suppressed by sevoflurane. Moreover, sevoflurane treatment significantly increased the Ca The present study demonstrated that sevoflurane inhibited glioma tumorigenesis and modulated the cancer stem cell-like properties and mitochondrial membrane potential via activation of Ca

Identifiants

pubmed: 32360621
pii: S0024-3205(20)30423-9
doi: 10.1016/j.lfs.2020.117675
pii:
doi:

Substances chimiques

Chelating Agents 0
Reactive Oxygen Species 0
1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 139890-68-9
Sevoflurane 38LVP0K73A
Egtazic Acid 526U7A2651
Calcium-Calmodulin-Dependent Protein Kinase Type 2 EC 2.7.11.17
MAP Kinase Kinase 4 EC 2.7.12.2
Calcium SY7Q814VUP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117675

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no conflict of interest

Auteurs

Xue-Chang Han (XC)

The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, No. 24 JingHua Road, Jianxi District, Luoyang 471003, Henan Province, China. Electronic address: xuechanghandoc@sina.com.

Ya-Jie Zhang (YJ)

The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, No. 24 JingHua Road, Jianxi District, Luoyang 471003, Henan Province, China.

Xu Dong (X)

The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, No. 24 JingHua Road, Jianxi District, Luoyang 471003, Henan Province, China.

Qun-Zhi Xing (QZ)

The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, No. 24 JingHua Road, Jianxi District, Luoyang 471003, Henan Province, China.

Ke-Han Li (KH)

The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, No. 24 JingHua Road, Jianxi District, Luoyang 471003, Henan Province, China.

Lu Zhang (L)

The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, No. 24 JingHua Road, Jianxi District, Luoyang 471003, Henan Province, China.

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Classifications MeSH