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High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer
Increased copy numbers of 17q23 chromosomal region have been shown to occur in different tumour types and to be associated with tumour progression and with poor prognosis. Several genes have earlier been proposed as potential oncogenes at this region largely on the grounds of cell lines studies. In...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360139/ https://www.ncbi.nlm.nih.gov/pubmed/17353917 http://dx.doi.org/10.1038/sj.bjc.6603692 |
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author | Pärssinen, J Kuukasjärvi, T Karhu, R Kallioniemi, A |
author_facet | Pärssinen, J Kuukasjärvi, T Karhu, R Kallioniemi, A |
author_sort | Pärssinen, J |
collection | PubMed |
description | Increased copy numbers of 17q23 chromosomal region have been shown to occur in different tumour types and to be associated with tumour progression and with poor prognosis. Several genes have earlier been proposed as potential oncogenes at this region largely on the grounds of cell lines studies. In this study, we performed a systematic gene expression survey on 26 primary breast tumours with known 17q23 amplification status by quantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR). The 17q23 amplicon is restricted to an ∼5 MB region in breast cancer and contains 29 known genes. Our survey revealed a statistically significant (P<0.01) difference between the high level and no amplification groups in a set of eleven genes whereas no difference between the moderate and the non-amplified tumour groups were observed. Interestingly, these 11 genes were located adjacent to one another within a 1.56 Mb core region in which all except one of the genes were overexpressed. These data suggest that only high-level amplification at the 17q23 amplicon core leads to elevated gene expression in breast cancer. Moreover, our results highlight the fact that 17q23 amplicon carries multiple candidate genes and that this may be a more common event in gene amplification than previously thought. |
format | Text |
id | pubmed-2360139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23601392009-09-10 High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer Pärssinen, J Kuukasjärvi, T Karhu, R Kallioniemi, A Br J Cancer Genetics and Genomics Increased copy numbers of 17q23 chromosomal region have been shown to occur in different tumour types and to be associated with tumour progression and with poor prognosis. Several genes have earlier been proposed as potential oncogenes at this region largely on the grounds of cell lines studies. In this study, we performed a systematic gene expression survey on 26 primary breast tumours with known 17q23 amplification status by quantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR). The 17q23 amplicon is restricted to an ∼5 MB region in breast cancer and contains 29 known genes. Our survey revealed a statistically significant (P<0.01) difference between the high level and no amplification groups in a set of eleven genes whereas no difference between the moderate and the non-amplified tumour groups were observed. Interestingly, these 11 genes were located adjacent to one another within a 1.56 Mb core region in which all except one of the genes were overexpressed. These data suggest that only high-level amplification at the 17q23 amplicon core leads to elevated gene expression in breast cancer. Moreover, our results highlight the fact that 17q23 amplicon carries multiple candidate genes and that this may be a more common event in gene amplification than previously thought. Nature Publishing Group 2007-04-23 2007-03-13 /pmc/articles/PMC2360139/ /pubmed/17353917 http://dx.doi.org/10.1038/sj.bjc.6603692 Text en Copyright © 2007 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 Pärssinen, J Kuukasjärvi, T Karhu, R Kallioniemi, A High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer |
title | High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer |
title_full | High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer |
title_fullStr | High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer |
title_full_unstemmed | High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer |
title_short | High-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer |
title_sort | high-level amplification at 17q23 leads to coordinated overexpression of multiple adjacent genes in breast cancer |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360139/ https://www.ncbi.nlm.nih.gov/pubmed/17353917 http://dx.doi.org/10.1038/sj.bjc.6603692 |
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