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Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine
Targeted cancer therapy requires the rapid and accurate identification of genetic abnormalities predictive of therapeutic response. We sought to develop a high-throughput genotyping platform that would allow prospective patient selection to the best available therapies, and that could readily and in...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377316/ https://www.ncbi.nlm.nih.gov/pubmed/20432502 http://dx.doi.org/10.1002/emmm.201000070 |
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author | Dias-Santagata, Dora Akhavanfard, Sara David, Serena S Vernovsky, Kathy Kuhlmann, Georgiana Boisvert, Susan L Stubbs, Hannah McDermott, Ultan Settleman, Jeffrey Kwak, Eunice L Clark, Jeffrey W Isakoff, Steven J Sequist, Lecia V Engelman, Jeffrey A Lynch, Thomas J Haber, Daniel A Louis, David N Ellisen, Leif W Borger, Darrell R Iafrate, A John |
author_facet | Dias-Santagata, Dora Akhavanfard, Sara David, Serena S Vernovsky, Kathy Kuhlmann, Georgiana Boisvert, Susan L Stubbs, Hannah McDermott, Ultan Settleman, Jeffrey Kwak, Eunice L Clark, Jeffrey W Isakoff, Steven J Sequist, Lecia V Engelman, Jeffrey A Lynch, Thomas J Haber, Daniel A Louis, David N Ellisen, Leif W Borger, Darrell R Iafrate, A John |
author_sort | Dias-Santagata, Dora |
collection | PubMed |
description | Targeted cancer therapy requires the rapid and accurate identification of genetic abnormalities predictive of therapeutic response. We sought to develop a high-throughput genotyping platform that would allow prospective patient selection to the best available therapies, and that could readily and inexpensively be adopted by most clinical laboratories. We developed a highly sensitive multiplexed clinical assay that performs very well with nucleic acid derived from formalin fixation and paraffin embedding (FFPE) tissue, and tests for 120 previously described mutations in 13 cancer genes. Genetic profiling of 250 primary tumours was consistent with the documented oncogene mutational spectrum and identified rare events in some cancer types. The assay is currently being used for clinical testing of tumour samples and contributing to cancer patient management. This work therefore establishes a platform for real-time targeted genotyping that can be widely adopted. We expect that efforts like this one will play an increasingly important role in cancer management. |
format | Online Article Text |
id | pubmed-3377316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-33773162012-09-17 Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine Dias-Santagata, Dora Akhavanfard, Sara David, Serena S Vernovsky, Kathy Kuhlmann, Georgiana Boisvert, Susan L Stubbs, Hannah McDermott, Ultan Settleman, Jeffrey Kwak, Eunice L Clark, Jeffrey W Isakoff, Steven J Sequist, Lecia V Engelman, Jeffrey A Lynch, Thomas J Haber, Daniel A Louis, David N Ellisen, Leif W Borger, Darrell R Iafrate, A John EMBO Mol Med Reports Targeted cancer therapy requires the rapid and accurate identification of genetic abnormalities predictive of therapeutic response. We sought to develop a high-throughput genotyping platform that would allow prospective patient selection to the best available therapies, and that could readily and inexpensively be adopted by most clinical laboratories. We developed a highly sensitive multiplexed clinical assay that performs very well with nucleic acid derived from formalin fixation and paraffin embedding (FFPE) tissue, and tests for 120 previously described mutations in 13 cancer genes. Genetic profiling of 250 primary tumours was consistent with the documented oncogene mutational spectrum and identified rare events in some cancer types. The assay is currently being used for clinical testing of tumour samples and contributing to cancer patient management. This work therefore establishes a platform for real-time targeted genotyping that can be widely adopted. We expect that efforts like this one will play an increasingly important role in cancer management. WILEY-VCH Verlag 2010-05 /pmc/articles/PMC3377316/ /pubmed/20432502 http://dx.doi.org/10.1002/emmm.201000070 Text en Copyright © 2010 EMBO Molecular Medicine |
spellingShingle | Reports Dias-Santagata, Dora Akhavanfard, Sara David, Serena S Vernovsky, Kathy Kuhlmann, Georgiana Boisvert, Susan L Stubbs, Hannah McDermott, Ultan Settleman, Jeffrey Kwak, Eunice L Clark, Jeffrey W Isakoff, Steven J Sequist, Lecia V Engelman, Jeffrey A Lynch, Thomas J Haber, Daniel A Louis, David N Ellisen, Leif W Borger, Darrell R Iafrate, A John Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine |
title | Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine |
title_full | Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine |
title_fullStr | Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine |
title_full_unstemmed | Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine |
title_short | Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine |
title_sort | rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine |
topic | Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377316/ https://www.ncbi.nlm.nih.gov/pubmed/20432502 http://dx.doi.org/10.1002/emmm.201000070 |
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