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Recognition of Transmembrane Protein 39A as a Tumor-Specific Marker in Brain Tumor

Transmembrane protein 39A (TMEM39A) belongs to the TMEM39 family. TMEM39A gene is a susceptibility locus for multiple sclerosis. In addition, TMEM39A seems to be implicated in systemic lupus erythematosus. However, any possible involvement of TMEM39A in cancer remains largely unknown. In the present...

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Autores principales: Park, Jisoo, Lee, Hyunji, Tran, Quangdon, Mun, Kisun, Kim, Dohoon, Hong, Youngeun, Kwon, So Hee, Brazil, Derek, Park, Jongsun, Kim, Seon-Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Toxicology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266369/
https://www.ncbi.nlm.nih.gov/pubmed/28133515
http://dx.doi.org/10.5487/TR.2017.33.1.063
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author Park, Jisoo
Lee, Hyunji
Tran, Quangdon
Mun, Kisun
Kim, Dohoon
Hong, Youngeun
Kwon, So Hee
Brazil, Derek
Park, Jongsun
Kim, Seon-Hwan
author_facet Park, Jisoo
Lee, Hyunji
Tran, Quangdon
Mun, Kisun
Kim, Dohoon
Hong, Youngeun
Kwon, So Hee
Brazil, Derek
Park, Jongsun
Kim, Seon-Hwan
author_sort Park, Jisoo
collection PubMed
description Transmembrane protein 39A (TMEM39A) belongs to the TMEM39 family. TMEM39A gene is a susceptibility locus for multiple sclerosis. In addition, TMEM39A seems to be implicated in systemic lupus erythematosus. However, any possible involvement of TMEM39A in cancer remains largely unknown. In the present report, we provide evidence that TMEM39A may play a role in brain tumors. Western blotting using an anti-TMEM39A antibody indicated that TMEM39A was overexpressed in glioblastoma cell lines, including U87-MG and U251-MG. Deep-sequencing transcriptomic profiling of U87-MG and U251-MG cells revealed that TMEM39A transcripts were upregulated in such cells compared with those of the cerebral cortex. Confocal microscopic analysis of U251-MG cells stained with anti-TMEM39A antibody showed that TMEM39A was located in dot-like structures lying close to the nucleus. TMEM39A probably located to mitochondria or to endosomes. Immunohistochemical analysis of glioma tissue specimens indicated that TMEM39A was markedly upregulated in such samples. Bioinformatic analysis of the Rembrandt knowledge base also supported upregulation of TMEM39A mRNA levels in glioma patients. Together, the results afford strong evidence that TMEM39A is upregulated in glioma cell lines and glioma tissue specimens. Therefore, TMEM39A may serve as a novel diagnostic marker of, and a therapeutic target for, gliomas and other cancers.
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spelling pubmed-52663692017-01-27 Recognition of Transmembrane Protein 39A as a Tumor-Specific Marker in Brain Tumor Park, Jisoo Lee, Hyunji Tran, Quangdon Mun, Kisun Kim, Dohoon Hong, Youngeun Kwon, So Hee Brazil, Derek Park, Jongsun Kim, Seon-Hwan Toxicol Res Original Article Transmembrane protein 39A (TMEM39A) belongs to the TMEM39 family. TMEM39A gene is a susceptibility locus for multiple sclerosis. In addition, TMEM39A seems to be implicated in systemic lupus erythematosus. However, any possible involvement of TMEM39A in cancer remains largely unknown. In the present report, we provide evidence that TMEM39A may play a role in brain tumors. Western blotting using an anti-TMEM39A antibody indicated that TMEM39A was overexpressed in glioblastoma cell lines, including U87-MG and U251-MG. Deep-sequencing transcriptomic profiling of U87-MG and U251-MG cells revealed that TMEM39A transcripts were upregulated in such cells compared with those of the cerebral cortex. Confocal microscopic analysis of U251-MG cells stained with anti-TMEM39A antibody showed that TMEM39A was located in dot-like structures lying close to the nucleus. TMEM39A probably located to mitochondria or to endosomes. Immunohistochemical analysis of glioma tissue specimens indicated that TMEM39A was markedly upregulated in such samples. Bioinformatic analysis of the Rembrandt knowledge base also supported upregulation of TMEM39A mRNA levels in glioma patients. Together, the results afford strong evidence that TMEM39A is upregulated in glioma cell lines and glioma tissue specimens. Therefore, TMEM39A may serve as a novel diagnostic marker of, and a therapeutic target for, gliomas and other cancers. Korean Society of Toxicology 2017-01 2017-01-15 /pmc/articles/PMC5266369/ /pubmed/28133515 http://dx.doi.org/10.5487/TR.2017.33.1.063 Text en Copyright © 2017 The Korean Society Of Toxicology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Jisoo
Lee, Hyunji
Tran, Quangdon
Mun, Kisun
Kim, Dohoon
Hong, Youngeun
Kwon, So Hee
Brazil, Derek
Park, Jongsun
Kim, Seon-Hwan
Recognition of Transmembrane Protein 39A as a Tumor-Specific Marker in Brain Tumor
title Recognition of Transmembrane Protein 39A as a Tumor-Specific Marker in Brain Tumor
title_full Recognition of Transmembrane Protein 39A as a Tumor-Specific Marker in Brain Tumor
title_fullStr Recognition of Transmembrane Protein 39A as a Tumor-Specific Marker in Brain Tumor
title_full_unstemmed Recognition of Transmembrane Protein 39A as a Tumor-Specific Marker in Brain Tumor
title_short Recognition of Transmembrane Protein 39A as a Tumor-Specific Marker in Brain Tumor
title_sort recognition of transmembrane protein 39a as a tumor-specific marker in brain tumor
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266369/
https://www.ncbi.nlm.nih.gov/pubmed/28133515
http://dx.doi.org/10.5487/TR.2017.33.1.063
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