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Expression of iron-related genes in human brain and brain tumors
BACKGROUND: Defective iron homeostasis may be involved in the development of some diseases within the central nervous system. Although the expression of genes involved in normal iron balance has been intensively studied in other tissues, little is known about their expression in the brain. We invest...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2679039/ https://www.ncbi.nlm.nih.gov/pubmed/19386095 http://dx.doi.org/10.1186/1471-2202-10-36 |
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author | Hänninen, Milla M Haapasalo, Joonas Haapasalo, Hannu Fleming, Robert E Britton, Robert S Bacon, Bruce R Parkkila, Seppo |
author_facet | Hänninen, Milla M Haapasalo, Joonas Haapasalo, Hannu Fleming, Robert E Britton, Robert S Bacon, Bruce R Parkkila, Seppo |
author_sort | Hänninen, Milla M |
collection | PubMed |
description | BACKGROUND: Defective iron homeostasis may be involved in the development of some diseases within the central nervous system. Although the expression of genes involved in normal iron balance has been intensively studied in other tissues, little is known about their expression in the brain. We investigated the mRNA levels of hepcidin (HAMP), HFE, neogenin (NEO1), transferrin receptor 1 (TFRC), transferrin receptor 2 (TFR2), and hemojuvelin (HFE2) in normal human brain, brain tumors, and astrocytoma cell lines. The specimens included 5 normal brain tissue samples, 4 meningiomas, one medulloblastoma, 3 oligodendrocytic gliomas, 2 oligoastrocytic gliomas, 8 astrocytic gliomas, and 3 astrocytoma cell lines. RESULTS: Except for hemojuvelin, all genes studied had detectable levels of mRNA. In most tumor types, the pattern of gene expression was diverse. Notable findings include high expression of transferrin receptor 1 in the hippocampus and medulla oblongata compared to other brain regions, low expression of HFE in normal brain with elevated HFE expression in meningiomas, and absence of hepcidin mRNA in astrocytoma cell lines despite expression in normal brain and tumor specimens. CONCLUSION: These results indicate that several iron-related genes are expressed in normal brain, and that their expression may be dysregulated in brain tumors. |
format | Text |
id | pubmed-2679039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26790392009-05-08 Expression of iron-related genes in human brain and brain tumors Hänninen, Milla M Haapasalo, Joonas Haapasalo, Hannu Fleming, Robert E Britton, Robert S Bacon, Bruce R Parkkila, Seppo BMC Neurosci Research Article BACKGROUND: Defective iron homeostasis may be involved in the development of some diseases within the central nervous system. Although the expression of genes involved in normal iron balance has been intensively studied in other tissues, little is known about their expression in the brain. We investigated the mRNA levels of hepcidin (HAMP), HFE, neogenin (NEO1), transferrin receptor 1 (TFRC), transferrin receptor 2 (TFR2), and hemojuvelin (HFE2) in normal human brain, brain tumors, and astrocytoma cell lines. The specimens included 5 normal brain tissue samples, 4 meningiomas, one medulloblastoma, 3 oligodendrocytic gliomas, 2 oligoastrocytic gliomas, 8 astrocytic gliomas, and 3 astrocytoma cell lines. RESULTS: Except for hemojuvelin, all genes studied had detectable levels of mRNA. In most tumor types, the pattern of gene expression was diverse. Notable findings include high expression of transferrin receptor 1 in the hippocampus and medulla oblongata compared to other brain regions, low expression of HFE in normal brain with elevated HFE expression in meningiomas, and absence of hepcidin mRNA in astrocytoma cell lines despite expression in normal brain and tumor specimens. CONCLUSION: These results indicate that several iron-related genes are expressed in normal brain, and that their expression may be dysregulated in brain tumors. BioMed Central 2009-04-22 /pmc/articles/PMC2679039/ /pubmed/19386095 http://dx.doi.org/10.1186/1471-2202-10-36 Text en Copyright © 2009 Hänninen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hänninen, Milla M Haapasalo, Joonas Haapasalo, Hannu Fleming, Robert E Britton, Robert S Bacon, Bruce R Parkkila, Seppo Expression of iron-related genes in human brain and brain tumors |
title | Expression of iron-related genes in human brain and brain tumors |
title_full | Expression of iron-related genes in human brain and brain tumors |
title_fullStr | Expression of iron-related genes in human brain and brain tumors |
title_full_unstemmed | Expression of iron-related genes in human brain and brain tumors |
title_short | Expression of iron-related genes in human brain and brain tumors |
title_sort | expression of iron-related genes in human brain and brain tumors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2679039/ https://www.ncbi.nlm.nih.gov/pubmed/19386095 http://dx.doi.org/10.1186/1471-2202-10-36 |
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