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GATA factors in human neuroblastoma: distinctive expression patterns in clinical subtypes
BACKGROUND: The aim of this study is to elucidate the expression patterns of GATA transcription factors in neuroblastoma and the developing sympathetic nervous system (SNS). METHODS: GATA-2, -3 and -4 and their cofactor friend-of-GATA (FOG)-2 were investigated in primary neuroblastoma by immunohisto...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768442/ https://www.ncbi.nlm.nih.gov/pubmed/19707195 http://dx.doi.org/10.1038/sj.bjc.6605276 |
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author | Hoene, V Fischer, M Ivanova, A Wallach, T Berthold, F Dame, C |
author_facet | Hoene, V Fischer, M Ivanova, A Wallach, T Berthold, F Dame, C |
author_sort | Hoene, V |
collection | PubMed |
description | BACKGROUND: The aim of this study is to elucidate the expression patterns of GATA transcription factors in neuroblastoma and the developing sympathetic nervous system (SNS). METHODS: GATA-2, -3 and -4 and their cofactor friend-of-GATA (FOG)-2 were investigated in primary neuroblastoma by immunohistochemistry, real-time RT-PCR (n=73) and microarray analysis (n=251). In addition, GATA-2, -3 and FOG-2 expression was determined by northern-blot hybridisation. In the developing murine SNS, Gata-4 and Fog-2 were examined by immunohistochemistry. RESULTS: Although Gata-2, -3 and Fog-2 are expressed in the developing nervous system, Gata-4 was not detected. In contrast, protein expression of all factors was observed in human neuroblastoma. Northern-blot hybridisation and real-time RT-PCR suggested specific expression patterns of the four genes in primary neuroblastoma, but did not show unequivocal results. In the large cohort examined by microarrays, a significant association of GATA-2, -3 and FOG-2 expression with low-risk features was observed, whereas GATA-4 mRNA levels correlated with MYCN-amplification. CONCLUSION: The transcription factors GATA-2 and -3, which are essential for normal SNS development, and their cofactor FOG-2 are downregulated in aggressive but not in favourable neuroblastoma. In contrast, upregulation of GATA-4 appears to be a common feature of this malignancy and might contribute to neuroblastoma pathogenesis. |
format | Text |
id | pubmed-2768442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-27684422010-10-20 GATA factors in human neuroblastoma: distinctive expression patterns in clinical subtypes Hoene, V Fischer, M Ivanova, A Wallach, T Berthold, F Dame, C Br J Cancer Genetics and Genomics BACKGROUND: The aim of this study is to elucidate the expression patterns of GATA transcription factors in neuroblastoma and the developing sympathetic nervous system (SNS). METHODS: GATA-2, -3 and -4 and their cofactor friend-of-GATA (FOG)-2 were investigated in primary neuroblastoma by immunohistochemistry, real-time RT-PCR (n=73) and microarray analysis (n=251). In addition, GATA-2, -3 and FOG-2 expression was determined by northern-blot hybridisation. In the developing murine SNS, Gata-4 and Fog-2 were examined by immunohistochemistry. RESULTS: Although Gata-2, -3 and Fog-2 are expressed in the developing nervous system, Gata-4 was not detected. In contrast, protein expression of all factors was observed in human neuroblastoma. Northern-blot hybridisation and real-time RT-PCR suggested specific expression patterns of the four genes in primary neuroblastoma, but did not show unequivocal results. In the large cohort examined by microarrays, a significant association of GATA-2, -3 and FOG-2 expression with low-risk features was observed, whereas GATA-4 mRNA levels correlated with MYCN-amplification. CONCLUSION: The transcription factors GATA-2 and -3, which are essential for normal SNS development, and their cofactor FOG-2 are downregulated in aggressive but not in favourable neuroblastoma. In contrast, upregulation of GATA-4 appears to be a common feature of this malignancy and might contribute to neuroblastoma pathogenesis. Nature Publishing Group 2009-10-20 2009-08-25 /pmc/articles/PMC2768442/ /pubmed/19707195 http://dx.doi.org/10.1038/sj.bjc.6605276 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Genetics and Genomics Hoene, V Fischer, M Ivanova, A Wallach, T Berthold, F Dame, C GATA factors in human neuroblastoma: distinctive expression patterns in clinical subtypes |
title | GATA factors in human neuroblastoma: distinctive expression patterns in clinical subtypes |
title_full | GATA factors in human neuroblastoma: distinctive expression patterns in clinical subtypes |
title_fullStr | GATA factors in human neuroblastoma: distinctive expression patterns in clinical subtypes |
title_full_unstemmed | GATA factors in human neuroblastoma: distinctive expression patterns in clinical subtypes |
title_short | GATA factors in human neuroblastoma: distinctive expression patterns in clinical subtypes |
title_sort | gata factors in human neuroblastoma: distinctive expression patterns in clinical subtypes |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768442/ https://www.ncbi.nlm.nih.gov/pubmed/19707195 http://dx.doi.org/10.1038/sj.bjc.6605276 |
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