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dc.contributor.authorBenjamin, David C
dc.contributor.authorKang, Joon Ho
dc.contributor.authorHamza, Bashar
dc.contributor.authorKing, Emily M
dc.contributor.authorLamar, John M
dc.contributor.authorManalis, Scott R
dc.contributor.authorHynes, Richard O
dc.date.accessioned2021-10-27T19:51:59Z
dc.date.available2021-10-27T19:51:59Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/133297
dc.description.abstractThe oncogene YAP has been shown previously to promote tumor growth and metastasis. However, how YAP influences the behavior of tumor cells traveling within the circulatory system has not been as well explored. Given that rate-limiting steps of metastasis are known to occur while tumor cells enter, travel through, or exit circulation, we sought to study how YAP influences tumor cell behavior within the circulatory system. Intravital imaging in live zebrafish embryos revealed that YAP influenced the distribution of tumor cells within the animal following intravenous injection. Control cells became lodged in the first capillary bed encountered in the tail, whereas cells overexpressing constitutively active YAP were able to travel through this capillary plexus, reenter systemic circulation, and seed in the brain. YAP controlled transit through these capillaries by promoting active migration within the vasculature. These results were corroborated in a mouse model following intravenous injection, where active YAP increased the number of circulating tumor cells over time. Our results suggest a possible mechanism whereby tumor cells can spread to organs beyond the first capillary bed downstream from the primary tumor. These results also show that a specific gene can affect the distribution of tumor cells within an animal, thereby influencing the global pattern of metastasis in that animal.
dc.language.isoen
dc.publisherAmerican Association for Cancer Research (AACR)
dc.relation.isversionof10.1158/0008-5472.CAN-20-0212
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.sourcePMC
dc.titleYAP Enhances Tumor Cell Dissemination by Promoting Intravascular Motility and Reentry into Systemic Circulation
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentHoward Hughes Medical Institute
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physics
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineering
dc.relation.journalCancer Research
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-07-16T17:14:08Z
dspace.orderedauthorsBenjamin, DC; Kang, JH; Hamza, B; King, EM; Lamar, JM; Manalis, SR; Hynes, RO
dspace.date.submission2021-07-16T17:14:10Z
mit.journal.volume80
mit.journal.issue18
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


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