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We are analyzing https://www.nature.com/articles/6691458.

Title:
Molecular cytogenetic analysis of breast cancer cell lines | British Journal of Cancer
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 . Β© 2000 Cancer Research Campaign
Website Age:
30 years and 10 months (reg. 1994-08-11).

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Custom-built

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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$63,100 per month
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Keywords {πŸ”}

cancer, article, breast, google, scholar, cas, nature, cell, lines, chromosomes, human, analysis, chromosome, genes, karyotyping, content, genomic, res, cytogenetic, cookies, comparative, hybridization, research, chromosomal, spectral, kallioniemi, privacy, data, open, molecular, carcinomas, tumour, cgh, carcinoma, line, translocations, karyotypes, dutrillaux, journal, access, theillet, edwards, karyotype, primary, tumours, evolution, pubmed, dna, treatment, cells,

Topics {βœ’οΈ}

nature portfolio privacy policy val d'aurelle-paul larmarque nature genetics 12 nature genetics 15 advertising nature tumour development social media 0/ reprints combinatorial multi-fluor fish human tumor cells permissions comparative genomic hybridization polish women magdalena tumorigenic cell line personal data human epithelial cancers human breast adenocarcinoma chromosomal evolution breast tumour nuclei data protection karyotype patterns extensive chromosome rearrangements frequently involved chromosome chromosome banding studies privacy single-cell sequencing karyotyping human chromosomes primary breast cancer reverse chromosome painting haematological malignancies detected hidden chromosome abnormalities journals search log dna content chromosomal translocation fusing clonal chromosome abnormalities aneuploid karyotypes appeared normal karyotype derived stem cell characteristics steadily lost chromosomes steadily gained chromosomes genomic dna resolves hgl/nrg1 genes european economic area explore content classical cytogenetic banding lymph node metastases fgfr1 coamplification results le francois dez

Questions {❓}

  • Heim S (1996) Clonal chromosome abnormalities in neoplastic cells: evidence of genetic instability?

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:Molecular cytogenetic analysis of breast cancer cell lines
         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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      headline:Molecular cytogenetic analysis of breast cancer cell lines
      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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      name:Department of Pathology, University of Cambridge, Cambridge
      name:Department of Pathology, University of Cambridge, Cambridge
      name:Department of Pathology, University of Cambridge, Cambridge
      name:Equipe Genome et Cancer, UMR CNRS 5535, Centre de Recherche en Cancerologie, Val d'Aurelle-Paul Larmarque, Montpellier, France
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