Functional characterization of a panel of high-grade serous ovarian cancer cell lines as representative experimental models of the disease.

dc.contributor.authorHaley, James
dc.contributor.authorTomar, Sunil
dc.contributor.authorPulliam, Nicholas
dc.contributor.authorXiong, Sen
dc.contributor.authorPerkins, Susan M.
dc.contributor.authorKarpf, Adam R.
dc.contributor.authorMitra, Sumegha
dc.contributor.authorNephew, Kenneth P.
dc.contributor.authorMitra, Anirban K.
dc.contributor.departmentDepartment of Medical and Molecular Genetics, IU School of Medicineen_US
dc.date.accessioned2016-12-21T20:26:11Z
dc.date.available2016-12-21T20:26:11Z
dc.date.issued2016-05-31
dc.description.abstractGenomic analysis of ovarian cancer cell lines has revealed a panel that best represents the most common ovarian cancer subtype, high-grade serous ovarian cancer (HGSOC). However, these HGSOC-like cell lines have not been extensively applied by ovarian cancer researchers to date, and the most commonly used cell lines in the ovarian cancer field do not genetically resemble the major clinical type of the disease. For the HGSOC-like lines to serve as suitable models, they need to be characterized for common functional assays. To achieve that objective, we systematically studied a panel of HGSOC cells CAOV3, COV362, Kuramochi, OVCAR4, OVCAR5, OVCAR8, OVSAHO and SNU119 for migration, invasion, proliferation, clonogenicity, EMT phenotype and cisplatin resistance. They exhibited a range of efficacies and OVCAR5, OVCAR8 and Kuramochi were the most aggressive. SNU119 and OVSAHO cells demonstrated the lowest functional activities. Wide differences in expression of EMT markers were observed between cell lines. SNU119 were the most epithelial and OVCAR8 had the most mesenchymal phenotype. COV362 was the most resistant to cisplatin while CAOV3 was the most sensitive. Taken together, our systematic characterization represents a valuable resource to help guide the application of HGSOC cells by the cancer research community.en_US
dc.eprint.versionPublished versionen_US
dc.identifier.citationHaley, J., Tomar, S., Pulliam, N., Xiong, S., Perkins, S. M., Karpf, A. R., … Mitra, A. K. (2016). Functional characterization of a panel of high-grade serous ovarian cancer cell lines as representative experimental models of the disease. Oncotarget, 7(22), 32810–32820. https://doi.org/10.18632/oncotarget.9053en_US
dc.identifier.issn1949-2553en_US
dc.identifier.urihttps://hdl.handle.net/1805/11696
dc.language.isoen_USen_US
dc.publisherImpact Journalsen_US
dc.relation.isversionof10.18632/oncotarget.9053en_US
dc.relation.journalOncotargeten_US
dc.rightsAttribution 3.0 Unported
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/
dc.sourcePublisheren_US
dc.subjectclonogenicityen_US
dc.subjectinvasionen_US
dc.subjectmigrationen_US
dc.subjectovarian canceren_US
dc.subjectproliferationen_US
dc.titleFunctional characterization of a panel of high-grade serous ovarian cancer cell lines as representative experimental models of the disease.en_US
dc.typeArticleen_US
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