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Absence of rearrangements in the BRCA2 gene in human cancers
Mutations of BRCA2 in sporadic breast and ovarian carcinomas are exceedingly rare. This led to the suggestion that large genomic rearrangements could be involved. We performed Southern blots in genomic DNA from 130 primary breast cancers and 83 cancer cell lines (breast, ovarian, pancreatic and smal...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2001
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363698/ https://www.ncbi.nlm.nih.gov/pubmed/11161375 http://dx.doi.org/10.1054/bjoc.2000.1577 |
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author | Chin, S-F Wang, Q Puisieux, A Caldas, C |
author_facet | Chin, S-F Wang, Q Puisieux, A Caldas, C |
author_sort | Chin, S-F |
collection | PubMed |
description | Mutations of BRCA2 in sporadic breast and ovarian carcinomas are exceedingly rare. This led to the suggestion that large genomic rearrangements could be involved. We performed Southern blots in genomic DNA from 130 primary breast cancers and 83 cancer cell lines (breast, ovarian, pancreatic and small cell lung carcinomas) and found no genomic rearrangements. These results suggest that a gene other than BRCA2 is the target of the frequent 13q12.3 allelic deletions in human cancers. © 2001 Cancer Research Campaign http://www.bjcancer.com |
format | Text |
id | pubmed-2363698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23636982009-09-10 Absence of rearrangements in the BRCA2 gene in human cancers Chin, S-F Wang, Q Puisieux, A Caldas, C Br J Cancer Short Communication Mutations of BRCA2 in sporadic breast and ovarian carcinomas are exceedingly rare. This led to the suggestion that large genomic rearrangements could be involved. We performed Southern blots in genomic DNA from 130 primary breast cancers and 83 cancer cell lines (breast, ovarian, pancreatic and small cell lung carcinomas) and found no genomic rearrangements. These results suggest that a gene other than BRCA2 is the target of the frequent 13q12.3 allelic deletions in human cancers. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-01 /pmc/articles/PMC2363698/ /pubmed/11161375 http://dx.doi.org/10.1054/bjoc.2000.1577 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 | Short Communication Chin, S-F Wang, Q Puisieux, A Caldas, C Absence of rearrangements in the BRCA2 gene in human cancers |
title | Absence of rearrangements in the BRCA2 gene in human cancers |
title_full | Absence of rearrangements in the BRCA2 gene in human cancers |
title_fullStr | Absence of rearrangements in the BRCA2 gene in human cancers |
title_full_unstemmed | Absence of rearrangements in the BRCA2 gene in human cancers |
title_short | Absence of rearrangements in the BRCA2 gene in human cancers |
title_sort | absence of rearrangements in the brca2 gene in human cancers |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363698/ https://www.ncbi.nlm.nih.gov/pubmed/11161375 http://dx.doi.org/10.1054/bjoc.2000.1577 |
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