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Molecular cytogenetic analysis of breast cancer cell lines

The extensive chromosome rearrangements of breast carcinomas must contribute to tumour development, but have been largely intractable to classical cytogenetic banding. We report here the analysis by 24-colour karyotyping and comparative genomic hybridization (CGH) of 19 breast carcinoma cell lines a...

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Autores principales: Davidson, J M, Gorringe, K L, Chin, S-F, Orsetti, B, Besret, C, Courtay-Cahen, C, Roberts, I, Theillet, C, Caldas, C, Edwards, P A W
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408781/
https://www.ncbi.nlm.nih.gov/pubmed/11044355
http://dx.doi.org/10.1054/bjoc.2000.1458
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author Davidson, J M
Gorringe, K L
Chin, S-F
Orsetti, B
Besret, C
Courtay-Cahen, C
Roberts, I
Theillet, C
Caldas, C
Edwards, P A W
author_facet Davidson, J M
Gorringe, K L
Chin, S-F
Orsetti, B
Besret, C
Courtay-Cahen, C
Roberts, I
Theillet, C
Caldas, C
Edwards, P A W
author_sort Davidson, J M
collection PubMed
description The extensive chromosome rearrangements of breast carcinomas must contribute to tumour development, but have been largely intractable to classical cytogenetic banding. We report here the analysis by 24-colour karyotyping and comparative genomic hybridization (CGH) of 19 breast carcinoma cell lines and one normal breast epithelial cell line, which provide model examples of karyotype patterns and translocations present in breast carcinomas. The CGH was compared with CGH of 106 primary breast cancers. The lines varied from perfectly diploid to highly aneuploid. Translocations were very varied and over 98% were unbalanced. The most frequent in the carcinomas were 8;11 in five lines; and 8;17, 1;4 and 1;10 in four lines. The most frequently involved chromosome was 8. Several lines showed complex multiply-translocated chromosomes. The very aneuploid karyotypes appeared to fall into two groups that evolved by different routes: one that steadily lost chromosomes and at one point doubled their entire karyotype; and another that steadily gained chromosomes, together with abnormalities. All karyotypes fell within the range seen in fresh material and CGH confirmed that the lines were broadly representative of fresh tumours. The karyotypes provide a resource for the cataloguing and analysis of translocations in these tumours, accessible at http://www.path.cam.ac.uk/~pawefish. © 2000 Cancer Research Campaign
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spelling pubmed-24087812009-09-10 Molecular cytogenetic analysis of breast cancer cell lines Davidson, J M Gorringe, K L Chin, S-F Orsetti, B Besret, C Courtay-Cahen, C Roberts, I Theillet, C Caldas, C Edwards, P A W Br J Cancer Regular Article The extensive chromosome rearrangements of breast carcinomas must contribute to tumour development, but have been largely intractable to classical cytogenetic banding. We report here the analysis by 24-colour karyotyping and comparative genomic hybridization (CGH) of 19 breast carcinoma cell lines and one normal breast epithelial cell line, which provide model examples of karyotype patterns and translocations present in breast carcinomas. The CGH was compared with CGH of 106 primary breast cancers. The lines varied from perfectly diploid to highly aneuploid. Translocations were very varied and over 98% were unbalanced. The most frequent in the carcinomas were 8;11 in five lines; and 8;17, 1;4 and 1;10 in four lines. The most frequently involved chromosome was 8. Several lines showed complex multiply-translocated chromosomes. The very aneuploid karyotypes appeared to fall into two groups that evolved by different routes: one that steadily lost chromosomes and at one point doubled their entire karyotype; and another that steadily gained chromosomes, together with abnormalities. All karyotypes fell within the range seen in fresh material and CGH confirmed that the lines were broadly representative of fresh tumours. The karyotypes provide a resource for the cataloguing and analysis of translocations in these tumours, accessible at http://www.path.cam.ac.uk/~pawefish. © 2000 Cancer Research Campaign Nature Publishing Group 2000-11 2000-10-26 /pmc/articles/PMC2408781/ /pubmed/11044355 http://dx.doi.org/10.1054/bjoc.2000.1458 Text en Copyright © 2000 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
Davidson, J M
Gorringe, K L
Chin, S-F
Orsetti, B
Besret, C
Courtay-Cahen, C
Roberts, I
Theillet, C
Caldas, C
Edwards, P A W
Molecular cytogenetic analysis of breast cancer cell lines
title Molecular cytogenetic analysis of breast cancer cell lines
title_full Molecular cytogenetic analysis of breast cancer cell lines
title_fullStr Molecular cytogenetic analysis of breast cancer cell lines
title_full_unstemmed Molecular cytogenetic analysis of breast cancer cell lines
title_short Molecular cytogenetic analysis of breast cancer cell lines
title_sort molecular cytogenetic analysis of breast cancer cell lines
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408781/
https://www.ncbi.nlm.nih.gov/pubmed/11044355
http://dx.doi.org/10.1054/bjoc.2000.1458
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