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Published in: European Journal of Medical Research 1/2014

Open Access 01-12-2014 | Research

The roles of mitoferrin-2 in the process of arsenic trioxide-induced cell damage in human gliomas

Authors: Chunlei Wang, Xiaofeng Chen, Huichao Zou, Xin Chen, Yaohua Liu, Shiguang Zhao

Published in: European Journal of Medical Research | Issue 1/2014

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Abstract

Background

Among glioma treatment strategies, arsenic trioxide (As2O3) has shown efficacy as a therapeutic agent against human gliomas. However, the exact antitumor mechanism of action of As2O3 is still unclear. Mitochondria are considered to be the major source of intracellular reactive oxygen species (ROS), which are known to be associated with As2O3-induced cell damage. Therefore, we investigated whether mitoferrin-2, a mitochondrial iron uptake transporter, participates in As2O3-induced cell killing in human gliomas.

Methods

Human glioma cell lines were used to explore the mechanism of As2O3’s antitumor effects. First, expression of mitoferrin-2 was analyzed in glioma cells that were pretreated with As2O3. Changes in ROS production and apoptosis were assessed. Furthermore, cell viability was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT).

Results

In the present study we found that As2O3 induced ROS production and apoptosis in glioma cells. In addition, gene expression of mitoferrin-2, a mitochondrial iron uptake transporter, was increased 4 to 5 fold after exposure to As2O3 (5 μM) for 48 hours. Furthermore, apoptosis and cytotoxicity induced by As2O3 in glioma cells were decreased after silencing the mitoferrin-2 gene.

Conclusions

Our findings indicated that mitoferrin-2 participates in mitochondrial ROS-dependent mechanisms underlying As2O3-mediated damage in glioma cells.
Appendix
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Metadata
Title
The roles of mitoferrin-2 in the process of arsenic trioxide-induced cell damage in human gliomas
Authors
Chunlei Wang
Xiaofeng Chen
Huichao Zou
Xin Chen
Yaohua Liu
Shiguang Zhao
Publication date
01-12-2014
Publisher
BioMed Central
Published in
European Journal of Medical Research / Issue 1/2014
Electronic ISSN: 2047-783X
DOI
https://doi.org/10.1186/s40001-014-0049-5

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