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High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer

We have recently discovered that the nuclear matrix protein SAFB is an oestrogen receptor corepressor. Since it has become clear that many steroid receptor cofactors play important roles in breast tumorigenesis, we investigated whether SAFB could also be involved in breast cancer. To address this qu...

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Autores principales: Oesterreich, S, Allredl, D C, Mohsin, S K, Zhang, Q, Wong, H, Lee, A V, Osborne, C K, O'Connell, P
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363776/
https://www.ncbi.nlm.nih.gov/pubmed/11207044
http://dx.doi.org/10.1054/bjoc.2000.1606
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author Oesterreich, S
Allredl, D C
Mohsin, S K
Zhang, Q
Wong, H
Lee, A V
Osborne, C K
O'Connell, P
author_facet Oesterreich, S
Allredl, D C
Mohsin, S K
Zhang, Q
Wong, H
Lee, A V
Osborne, C K
O'Connell, P
author_sort Oesterreich, S
collection PubMed
description We have recently discovered that the nuclear matrix protein SAFB is an oestrogen receptor corepressor. Since it has become clear that many steroid receptor cofactors play important roles in breast tumorigenesis, we investigated whether SAFB could also be involved in breast cancer. To address this question, the gene locus was examined for structural alterations in breast cancer tissue. Laser capture microdissection was used for isolating DNA from paired primary breast tumour and normal tissue specimens, and the loss of heterozygosity (LOH) at chromosome 19p13.2–3 was determined by use of microsatellite markers. LOH was detected at the marker D19S216, which colocalizes with the SAFB locus, in specimens from 29 (78.4%) of 37 informative patients. The peak LOH rate occurred at D19S216 near the SAFB locus, with LOH frequencies ranging from 21.6% to 47.2% at other markers. The finding of a very high LOH rate at the marker D19S216 strongly indicates the presence of a breast tumour-suppressor gene locus. While preliminary findings of mutations in SAFB suggest that this indeed may be a promising candidate, other potential candidate genes are located at this locus. © 2001 Cancer Research Campaign http://www.bjcancer.com
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spelling pubmed-23637762009-09-10 High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer Oesterreich, S Allredl, D C Mohsin, S K Zhang, Q Wong, H Lee, A V Osborne, C K O'Connell, P Br J Cancer Regular Article We have recently discovered that the nuclear matrix protein SAFB is an oestrogen receptor corepressor. Since it has become clear that many steroid receptor cofactors play important roles in breast tumorigenesis, we investigated whether SAFB could also be involved in breast cancer. To address this question, the gene locus was examined for structural alterations in breast cancer tissue. Laser capture microdissection was used for isolating DNA from paired primary breast tumour and normal tissue specimens, and the loss of heterozygosity (LOH) at chromosome 19p13.2–3 was determined by use of microsatellite markers. LOH was detected at the marker D19S216, which colocalizes with the SAFB locus, in specimens from 29 (78.4%) of 37 informative patients. The peak LOH rate occurred at D19S216 near the SAFB locus, with LOH frequencies ranging from 21.6% to 47.2% at other markers. The finding of a very high LOH rate at the marker D19S216 strongly indicates the presence of a breast tumour-suppressor gene locus. While preliminary findings of mutations in SAFB suggest that this indeed may be a promising candidate, other potential candidate genes are located at this locus. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-02 /pmc/articles/PMC2363776/ /pubmed/11207044 http://dx.doi.org/10.1054/bjoc.2000.1606 Text en Copyright © 2001 Cancer Research Campaign 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 Regular Article
Oesterreich, S
Allredl, D C
Mohsin, S K
Zhang, Q
Wong, H
Lee, A V
Osborne, C K
O'Connell, P
High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer
title High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer
title_full High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer
title_fullStr High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer
title_full_unstemmed High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer
title_short High rates of loss of heterozygosity on chromosome 19p13 in human breast cancer
title_sort high rates of loss of heterozygosity on chromosome 19p13 in human breast cancer
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363776/
https://www.ncbi.nlm.nih.gov/pubmed/11207044
http://dx.doi.org/10.1054/bjoc.2000.1606
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