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dc.contributor.authorBruna, A
dc.contributor.authorRueda, OM
dc.contributor.authorGreenwood, W
dc.contributor.authorBatra, AS
dc.contributor.authorCallari, M
dc.contributor.authorBatra, RN
dc.contributor.authorPogrebniak, K
dc.contributor.authorSandoval, J
dc.contributor.authorCassidy, JW
dc.contributor.authorTufegdzic-Vidakovic, A
dc.contributor.authorSammut, S-J
dc.contributor.authorJones, L
dc.contributor.authorProvenzano, E
dc.contributor.authorBaird, R
dc.contributor.authorEirew, P
dc.contributor.authorHadfield, J
dc.contributor.authorEldridge, M
dc.contributor.authorMcLaren-Douglas, A
dc.contributor.authorBarthorpe, A
dc.contributor.authorLightfoot, H
dc.contributor.authorO'Connor, MJ
dc.contributor.authorGray, J
dc.contributor.authorCortes, J
dc.contributor.authorBaselga, J
dc.contributor.authorMarangoni, E
dc.contributor.authorWelm, AL
dc.contributor.authorAparicio, S
dc.contributor.authorSerra, V
dc.contributor.authorGarnett, MJ
dc.contributor.authorCaldas, C
dc.date.accessioned2020-08-04T13:58:18Z
dc.date.issued2016-09-22
dc.identifier.citationCell, 2016, 167 (1), pp. 260 - 274.e22
dc.identifier.issn0092-8674
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3894
dc.identifier.eissn1097-4172
dc.identifier.doi10.1016/j.cell.2016.08.041
dc.description.abstractThe inter- and intra-tumor heterogeneity of breast cancer needs to be adequately captured in pre-clinical models. We have created a large collection of breast cancer patient-derived tumor xenografts (PDTXs), in which the morphological and molecular characteristics of the originating tumor are preserved through passaging in the mouse. An integrated platform combining in vivo maintenance of these PDTXs along with short-term cultures of PDTX-derived tumor cells (PDTCs) was optimized. Remarkably, the intra-tumor genomic clonal architecture present in the originating breast cancers was mostly preserved upon serial passaging in xenografts and in short-term cultured PDTCs. We assessed drug responses in PDTCs on a high-throughput platform and validated several ex vivo responses in vivo. The biobank represents a powerful resource for pre-clinical breast cancer pharmacogenomic studies (http://caldaslab.cruk.cam.ac.uk/bcape), including identification of biomarkers of response or resistance.
dc.formatPrint-Electronic
dc.format.extent260 - 274.e22
dc.languageeng
dc.language.isoeng
dc.publisherCELL PRESS
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectTumor Cells, Cultured
dc.subjectAnimals
dc.subjectHumans
dc.subjectMice
dc.subjectBreast Neoplasms
dc.subjectXenograft Model Antitumor Assays
dc.subjectDrug Resistance, Neoplasm
dc.subjectBiological Specimen Banks
dc.subjectFemale
dc.subjectBiomarkers, Pharmacological
dc.subjectHigh-Throughput Screening Assays
dc.subjectPharmacogenomic Testing
dc.titleA Biobank of Breast Cancer Explants with Preserved Intra-tumor Heterogeneity to Screen Anticancer Compounds.
dc.typeJournal Article
dcterms.dateAccepted2016-08-18
rioxxterms.versionofrecord10.1016/j.cell.2016.08.041
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2016-09-15
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCell
pubs.issue1
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Preclinical Modelling of Paediatric Cancer Evolution
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Preclinical Modelling of Paediatric Cancer Evolution
pubs.publication-statusPublished
pubs.volume167
pubs.embargo.termsNot known
icr.researchteamPreclinical Modelling of Paediatric Cancer Evolution
dc.contributor.icrauthorBruna Cabot, Alejandra
dc.contributor.icrauthorSammut, Stephen John


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