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Characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours

Currently available human tumour cell line panels consist of a small number of lines in each lineage that generally fail to retain the phenotype of the original patient tumour. Here we develop a cell culture medium that enables us to routinely establish cell lines from diverse subtypes of human ovar...

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Autores principales: Ince, Tan A., Sousa, Aurea D., Jones, Michelle A., Harrell, J. Chuck, Agoston, Elin S., Krohn, Marit, Selfors, Laura M., Liu, Wenbin, Chen, Ken, Yong, Mao, Buchwald, Peter, Wang, Bin, Hale, Katherine S., Cohick, Evan, Sergent, Petra, Witt, Abigail, Kozhekbaeva, Zhanna, Gao, Sizhen, Agoston, Agoston T., Merritt, Melissa A., Foster, Rosemary, Rueda, Bo R., Crum, Christopher P., Brugge, Joan S., Mills, Gordon B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473807/
https://www.ncbi.nlm.nih.gov/pubmed/26080861
http://dx.doi.org/10.1038/ncomms8419
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author Ince, Tan A.
Sousa, Aurea D.
Jones, Michelle A.
Harrell, J. Chuck
Agoston, Elin S.
Krohn, Marit
Selfors, Laura M.
Liu, Wenbin
Chen, Ken
Yong, Mao
Buchwald, Peter
Wang, Bin
Hale, Katherine S.
Cohick, Evan
Sergent, Petra
Witt, Abigail
Kozhekbaeva, Zhanna
Gao, Sizhen
Agoston, Agoston T.
Merritt, Melissa A.
Foster, Rosemary
Rueda, Bo R.
Crum, Christopher P.
Brugge, Joan S.
Mills, Gordon B.
author_facet Ince, Tan A.
Sousa, Aurea D.
Jones, Michelle A.
Harrell, J. Chuck
Agoston, Elin S.
Krohn, Marit
Selfors, Laura M.
Liu, Wenbin
Chen, Ken
Yong, Mao
Buchwald, Peter
Wang, Bin
Hale, Katherine S.
Cohick, Evan
Sergent, Petra
Witt, Abigail
Kozhekbaeva, Zhanna
Gao, Sizhen
Agoston, Agoston T.
Merritt, Melissa A.
Foster, Rosemary
Rueda, Bo R.
Crum, Christopher P.
Brugge, Joan S.
Mills, Gordon B.
author_sort Ince, Tan A.
collection PubMed
description Currently available human tumour cell line panels consist of a small number of lines in each lineage that generally fail to retain the phenotype of the original patient tumour. Here we develop a cell culture medium that enables us to routinely establish cell lines from diverse subtypes of human ovarian cancers with >95% efficiency. Importantly, the 25 new ovarian tumour cell lines described here retain the genomic landscape, histopathology and molecular features of the original tumours. Furthermore, the molecular profile and drug response of these cell lines correlate with distinct groups of primary tumours with different outcomes. Thus, tumour cell lines derived using this methodology represent a significantly improved platform to study human tumour pathophysiology and response to therapy.
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spelling pubmed-44738072015-09-11 Characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours Ince, Tan A. Sousa, Aurea D. Jones, Michelle A. Harrell, J. Chuck Agoston, Elin S. Krohn, Marit Selfors, Laura M. Liu, Wenbin Chen, Ken Yong, Mao Buchwald, Peter Wang, Bin Hale, Katherine S. Cohick, Evan Sergent, Petra Witt, Abigail Kozhekbaeva, Zhanna Gao, Sizhen Agoston, Agoston T. Merritt, Melissa A. Foster, Rosemary Rueda, Bo R. Crum, Christopher P. Brugge, Joan S. Mills, Gordon B. Nat Commun Article Currently available human tumour cell line panels consist of a small number of lines in each lineage that generally fail to retain the phenotype of the original patient tumour. Here we develop a cell culture medium that enables us to routinely establish cell lines from diverse subtypes of human ovarian cancers with >95% efficiency. Importantly, the 25 new ovarian tumour cell lines described here retain the genomic landscape, histopathology and molecular features of the original tumours. Furthermore, the molecular profile and drug response of these cell lines correlate with distinct groups of primary tumours with different outcomes. Thus, tumour cell lines derived using this methodology represent a significantly improved platform to study human tumour pathophysiology and response to therapy. Nature Pub. Group 2015-06-17 /pmc/articles/PMC4473807/ /pubmed/26080861 http://dx.doi.org/10.1038/ncomms8419 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ince, Tan A.
Sousa, Aurea D.
Jones, Michelle A.
Harrell, J. Chuck
Agoston, Elin S.
Krohn, Marit
Selfors, Laura M.
Liu, Wenbin
Chen, Ken
Yong, Mao
Buchwald, Peter
Wang, Bin
Hale, Katherine S.
Cohick, Evan
Sergent, Petra
Witt, Abigail
Kozhekbaeva, Zhanna
Gao, Sizhen
Agoston, Agoston T.
Merritt, Melissa A.
Foster, Rosemary
Rueda, Bo R.
Crum, Christopher P.
Brugge, Joan S.
Mills, Gordon B.
Characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours
title Characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours
title_full Characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours
title_fullStr Characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours
title_full_unstemmed Characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours
title_short Characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours
title_sort characterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4473807/
https://www.ncbi.nlm.nih.gov/pubmed/26080861
http://dx.doi.org/10.1038/ncomms8419
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