A 3D inᅠvitro model of patient-derived prostate cancer xenograft for controlled interrogation of inᅠvivo tumor-stromal interactions

dc.citation.firstpage164en_US
dc.citation.journalTitleBiomaterialsen_US
dc.citation.lastpage172en_US
dc.citation.volumeNumber77en_US
dc.contributor.authorFong, Eliza L.S.en_US
dc.contributor.authorWan, Xinhaien_US
dc.contributor.authorYang, Junen_US
dc.contributor.authorMorgado, Micaelaen_US
dc.contributor.authorMikos, Antonios G.en_US
dc.contributor.authorHarrington, Daniel Antonen_US
dc.contributor.authorNavone, Nora M.en_US
dc.contributor.authorFarach-Carson, Mary C.en_US
dc.date.accessioned2017-02-01T18:55:23Zen_US
dc.date.available2017-02-01T18:55:23Zen_US
dc.date.issued2016en_US
dc.description.abstractPatient-derived xenograft (PDX) models better represent human cancer than traditional cell lines. However, the complex in vivo environment makes it challenging to employ PDX models to investigate tumor-stromal interactions, such as those that mediate prostate cancer (PCa) bone metastasis. Thus, we engineered a defined three-dimensional (3D) hydrogel system capable of supporting the co-culture of PCa PDX cells and osteoblastic cells to recapitulate the PCa-osteoblast unit within the bone metastatic microenvironment in vitro. Our 3D model not only maintained cell viability but also preserved the typical osteogenic phenotype of PCa PDX cells. Additionally, co-culture cellularity was maintained over that of either cell type cultured alone, suggesting that the PCa-osteoblast cross-talk supports PCa progression in bone, as is hypothesized to occur in patients with prostatic bone metastasis. Strikingly, osteoblastic cells co-cultured with PCa PDX tumoroids organized around the tumoroids, closely mimicking the architecture of PCa metastases in bone. Finally, tumor-stromal signaling mediated by the fibroblast growth factor axis tightly paralleled that in the in vivo counterpart. Together, these findings indicate that this 3D PCa PDX model recapitulates important pathological properties of PCa bone metastasis, and validate the use of this model for controlled and systematic interrogation of complex in vivo tumor-stromal interactions.en_US
dc.identifier.citationFong, Eliza L.S., Wan, Xinhai, Yang, Jun, et al.. "A 3D inᅠvitro model of patient-derived prostate cancer xenograft for controlled interrogation of inᅠvivo tumor-stromal interactions." <i>Biomaterials,</i> 77, (2016) Elsevier: 164-172. http://dx.doi.org/10.1016/j.biomaterials.2015.10.059.en_US
dc.identifier.doihttp://dx.doi.org/10.1016/j.biomaterials.2015.10.059en_US
dc.identifier.urihttps://hdl.handle.net/1911/93836en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsThis is an author's peer-reviewed final manuscript, as accepted by the publisher. The published article is copyrighted by Elsevier.en_US
dc.subject.keywordpatient-derived xenograften_US
dc.subject.keywordprostate canceren_US
dc.subject.keywordthree-dimensionalen_US
dc.subject.keywordco-cultureen_US
dc.subject.keywordosteoblastsen_US
dc.subject.keywordhydrogelen_US
dc.subject.keywordmodelen_US
dc.titleA 3D inᅠvitro model of patient-derived prostate cancer xenograft for controlled interrogation of inᅠvivo tumor-stromal interactionsen_US
dc.typeJournal articleen_US
dc.type.dcmiTexten_US
dc.type.publicationpost-printen_US
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