Integrated Proteomic Analysis of Human Cancer Cells and Plasma from Tumor Bearing Mice for Ovarian Cancer Biomarker Discovery

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Integrated Proteomic Analysis of Human Cancer Cells and Plasma from Tumor Bearing Mice for Ovarian Cancer Biomarker Discovery

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dc.contributor.author Pitteri, Sharon J.
dc.contributor.author JeBailey, Lellean
dc.contributor.author Faça, Vitor M.
dc.contributor.author Thorpe, Jason D.
dc.contributor.author Silva, Melissa A.
dc.contributor.author Ireton, Reneé C.
dc.contributor.author Horton, Marc B.
dc.contributor.author Pruitt, Liese C.
dc.contributor.author Urban, Nicole
dc.contributor.author Hanash, Samir M.
dc.contributor.author Nordheim, Alfred
dc.contributor.author Wang, Hong
dc.contributor.author Zhang, Qing
dc.contributor.author Cheng, Yu-Kang
dc.contributor.author Dinulescu, Daniela M
dc.date.accessioned 2011-05-19T20:09:05Z
dc.date.issued 2009
dc.identifier.citation Pitteri, Sharon J., Lellean JeBailey, Vitor M. Faça, Jason D. Thorpe, Melissa A. Silva, Reneé C. Ireton, Marc B. Horton, et al. 2009. Integrated Proteomic Analysis of Human Cancer Cells and Plasma from Tumor Bearing Mice for Ovarian Cancer Biomarker Discovery. PLoS ONE 4(11): e7916. en_US
dc.identifier.issn 1932-6203 en_US
dc.identifier.uri http://nrs.harvard.edu/urn-3:HUL.InstRepos:4892364
dc.description.abstract Background: The complexity of the human plasma proteome represents a substantial challenge for biomarker discovery. Proteomic analysis of genetically engineered mouse models of cancer and isolated cancer cells and cell lines provide alternative methods for identification of potential cancer markers that would be detectable in human blood using sensitive assays. The goal of this work is to evaluate the utility of an integrative strategy using these two approaches for biomarker discovery. Methodology/Principal Findings: We investigated a strategy that combined quantitative plasma proteomics of an ovarian cancer mouse model with analysis of proteins secreted or shed by human ovarian cancer cells. Of 106 plasma proteins identified with increased levels in tumor bearing mice, 58 were also secreted or shed from ovarian cancer cells. The remainder consisted primarily of host-response proteins. Of 25 proteins identified in the study that were assayed, 8 mostly secreted proteins common to mouse plasma and human cancer cells were significantly upregulated in a set of plasmas from ovarian cancer patients. Five of the eight proteins were confirmed to be upregulated in a second independent set of ovarian cancer plasmas, including in early stage disease. Conclusions/Significance: Integrated proteomic analysis of cancer mouse models and human cancer cell populations provides an effective approach to identify potential circulating protein biomarkers. en_US
dc.language.iso en_US en_US
dc.publisher Public Library of Science en_US
dc.relation.isversionof doi:10.1371/journal.pone.0007916 en_US
dc.relation.hasversion http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775948/pdf/ en_US
dash.license LAA
dc.subject biotechnology en_US
dc.subject protein chemistry and proteomics en_US
dc.subject oncology en_US
dc.subject gynecological cancers en_US
dc.subject women's health en_US
dc.title Integrated Proteomic Analysis of Human Cancer Cells and Plasma from Tumor Bearing Mice for Ovarian Cancer Biomarker Discovery en_US
dc.type Journal Article en_US
dc.description.version Version of Record en_US
dc.relation.journal PLoS ONE en_US
dash.depositing.author Cheng, Yu-Kang
dc.date.available 2011-05-19T20:09:05Z
dash.affiliation.other SPH^Biostatistics en_US
dash.affiliation.other HMS^Pathology en_US

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