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

TitleCharacterization of twenty-five ovarian tumour cell lines that phenocopy primary tumours.
Publication TypeJournal Article
Year of Publication2015
AuthorsInce TA, Sousa AD, Jones MA, J Harrell C, Agoston ES, Krohn M, Selfors LM, Liu W, Chen K, Yong M, Buchwald P, Wang B, Hale KS, Cohick E, Sergent P, Witt A, Kozhekbaeva Z, Gao S, Agoston AT, Merritt MA, Foster R, Rueda BR, Crum CP, Brugge JS, Mills GB
JournalNat Commun
Volume6
Pagination7419
Date Published2015 Jun 17
ISSN2041-1723
KeywordsCarcinoma, Cell Line, Tumor, Cisplatin, Culture Media, Drug Screening Assays, Antitumor, Female, Gene Expression Profiling, Heterografts, Humans, Ovarian Neoplasms, Paclitaxel, Phenotype
Abstract

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.

DOI10.1038/ncomms8419
Alternate JournalNat Commun
PubMed ID26080861
PubMed Central IDPMC4473807
Grant ListR01CA123219 / CA / NCI NIH HHS / United States
P30 CA016672 / CA / NCI NIH HHS / United States
R01-CA146445-01 / CA / NCI NIH HHS / United States
R01 CA146445 / CA / NCI NIH HHS / United States
R01 CA123219 / CA / NCI NIH HHS / United States
U01 CA168394 / CA / NCI NIH HHS / United States
P50 CA083639 / CA / NCI NIH HHS / United States
Related Faculty: 
Tan Ince, M.D., Ph.D.

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