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Anti-Tumor Effects of Mfn2 in Gastric Cancer

Mitofusin-2 (Mfn2) is a mitochondrial outer membrane protein involved in mitochondrial fusion. Its mutation can cause Charcot-Marie-Tooth disease. Recent studies of Mfn2 in cancer research have not included gastric cancer. We confirmed that Mfn2 expression was lower in tumor tissue than in normal ga...

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Autores principales: Zhang, Ge-Er, Jin, Hai-Long, Lin, Xian-Ke, Chen, Chao, Liu, Xiao-Sun, Zhang, Qing, Yu, Ji-Ren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742171/
https://www.ncbi.nlm.nih.gov/pubmed/23797661
http://dx.doi.org/10.3390/ijms140713005
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author Zhang, Ge-Er
Jin, Hai-Long
Lin, Xian-Ke
Chen, Chao
Liu, Xiao-Sun
Zhang, Qing
Yu, Ji-Ren
author_facet Zhang, Ge-Er
Jin, Hai-Long
Lin, Xian-Ke
Chen, Chao
Liu, Xiao-Sun
Zhang, Qing
Yu, Ji-Ren
author_sort Zhang, Ge-Er
collection PubMed
description Mitofusin-2 (Mfn2) is a mitochondrial outer membrane protein involved in mitochondrial fusion. Its mutation can cause Charcot-Marie-Tooth disease. Recent studies of Mfn2 in cancer research have not included gastric cancer. We confirmed that Mfn2 expression was lower in tumor tissue than in normal gastric mucosal tissue and that it was negatively correlated with tumor size, indicating an anti-tumor role for Mfn2. In vitro experiments showed that Mfn2 overexpression suppressed gastric cancer cell proliferation and colony formation, weakened the invasion and migratory ability of cancer cells by downregulating MMP-2 and MMP-9, halted the cell cycle and induced apoptosis. Western blotting indicated the likely involvement of P21 and PI3K/Akt signaling. Therefore, Mfn2 is a potential anti-tumor gene and a potential therapeutic target for treating gastric cancer. The progress of gastric cancer may be delayed by controlling Mfn2 expression.
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spelling pubmed-37421712013-08-13 Anti-Tumor Effects of Mfn2 in Gastric Cancer Zhang, Ge-Er Jin, Hai-Long Lin, Xian-Ke Chen, Chao Liu, Xiao-Sun Zhang, Qing Yu, Ji-Ren Int J Mol Sci Article Mitofusin-2 (Mfn2) is a mitochondrial outer membrane protein involved in mitochondrial fusion. Its mutation can cause Charcot-Marie-Tooth disease. Recent studies of Mfn2 in cancer research have not included gastric cancer. We confirmed that Mfn2 expression was lower in tumor tissue than in normal gastric mucosal tissue and that it was negatively correlated with tumor size, indicating an anti-tumor role for Mfn2. In vitro experiments showed that Mfn2 overexpression suppressed gastric cancer cell proliferation and colony formation, weakened the invasion and migratory ability of cancer cells by downregulating MMP-2 and MMP-9, halted the cell cycle and induced apoptosis. Western blotting indicated the likely involvement of P21 and PI3K/Akt signaling. Therefore, Mfn2 is a potential anti-tumor gene and a potential therapeutic target for treating gastric cancer. The progress of gastric cancer may be delayed by controlling Mfn2 expression. Molecular Diversity Preservation International (MDPI) 2013-06-24 /pmc/articles/PMC3742171/ /pubmed/23797661 http://dx.doi.org/10.3390/ijms140713005 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Zhang, Ge-Er
Jin, Hai-Long
Lin, Xian-Ke
Chen, Chao
Liu, Xiao-Sun
Zhang, Qing
Yu, Ji-Ren
Anti-Tumor Effects of Mfn2 in Gastric Cancer
title Anti-Tumor Effects of Mfn2 in Gastric Cancer
title_full Anti-Tumor Effects of Mfn2 in Gastric Cancer
title_fullStr Anti-Tumor Effects of Mfn2 in Gastric Cancer
title_full_unstemmed Anti-Tumor Effects of Mfn2 in Gastric Cancer
title_short Anti-Tumor Effects of Mfn2 in Gastric Cancer
title_sort anti-tumor effects of mfn2 in gastric cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742171/
https://www.ncbi.nlm.nih.gov/pubmed/23797661
http://dx.doi.org/10.3390/ijms140713005
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