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dc.contributor.authorBrooks, M. W.
dc.contributor.authorArdolino, M.
dc.contributor.authorFessler, E.
dc.contributor.authorKrall, J. A.
dc.contributor.authorDeCock, J.
dc.contributor.authorIannello, A.
dc.contributor.authorIwamoto, Y.
dc.contributor.authorCortez-Retamozo, V.
dc.contributor.authorPittet, M. J.
dc.contributor.authorRaulet, D. H.
dc.contributor.authorSpiegel, Asaf
dc.contributor.authorHoushyar, Samin
dc.contributor.authorReinhardt, Ferenc
dc.contributor.authorChen, Michelle B
dc.contributor.authorZervantonakis, Ioannis
dc.contributor.authorKamm, Roger Dale
dc.contributor.authorWeinberg, Robert A
dc.date.accessioned2018-07-13T14:50:01Z
dc.date.available2018-07-13T14:50:01Z
dc.date.issued2016-04
dc.identifier.issn2159-8274
dc.identifier.issn2159-8290
dc.identifier.urihttp://hdl.handle.net/1721.1/116973
dc.description.abstractImmune cells promote the initial metastatic dissemination of carcinoma cells from primary tumors. In contrast to their well-studied functions in the initial stages of metastasis, the specific roles of immunocytes in facilitating progression through the critical later steps of the invasion–metastasis cascade remain poorly understood. Here, we define novel functions of neutrophils in promoting intraluminal survival and extravasation at sites of metastatic dissemination. We show that CD11b+/Ly6G+neutrophils enhance metastasis formation via two distinct mechanisms. First, neutrophils inhibit natural killer cell function, which leads to a significant increase in the intraluminal survival time of tumor cells. Thereafter, neutrophils operate to facilitate extravasation of tumor cells through the secretion of IL1β and matrix metalloproteinases. These results identify neutrophils as key regulators of intraluminal survival and extravasation through their cross-talk with host cells and disseminating carcinoma cells. SIGNIFICANCE: This study provides important insights into the systemic contributions of neutrophils to cancer metastasis by identifying how neutrophils facilitate intermediate steps of the invasion–metastasis cascade. We demonstrate that neutrophils suppress natural killer cell activity and increase extravasation of tumor cells.en_US
dc.description.sponsorshipHuman Frontier Science Program (Strasbourg, France) (fellowship LT00728/2008-L)en_US
dc.description.sponsorshipCharles King Trust Foundationen_US
dc.description.sponsorshipMassachusetts Institute of Technology. Ludwig Center for Cancer Researchen_US
dc.description.sponsorshipCancer Research Institute (New York, N.Y.) (Irvington Fellowship)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant P01 CA080111)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant CA163109)en_US
dc.publisherAmerican Association for Cancer Research (AACR)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1158/2159-8290.CD-15-1157en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleNeutrophils Suppress Intraluminal NK Cell-Mediated Tumor Cell Clearance and Enhance Extravasation of Disseminated Carcinoma Cellsen_US
dc.typeArticleen_US
dc.identifier.citationSpiegel, A., M. W. Brooks, S. Houshyar, F. Reinhardt, M. Ardolino, E. Fessler, M. B. Chen, et al. “Neutrophils Suppress Intraluminal NK Cell-Mediated Tumor Cell Clearance and Enhance Extravasation of Disseminated Carcinoma Cells.” Cancer Discovery 6, no. 6 (April 12, 2016): 630–649.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Division of Comparative Medicineen_US
dc.contributor.mitauthorSpiegel, Asaf
dc.contributor.mitauthorHoushyar, Samin
dc.contributor.mitauthorReinhardt, Ferenc
dc.contributor.mitauthorChen, Michelle B
dc.contributor.mitauthorZervantonakis, Ioannis
dc.contributor.mitauthorKamm, Roger Dale
dc.contributor.mitauthorWeinberg, Robert A
dc.relation.journalCancer Discoveryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-07-12T16:13:10Z
dspace.orderedauthorsSpiegel, A.; Brooks, M. W.; Houshyar, S.; Reinhardt, F.; Ardolino, M.; Fessler, E.; Chen, M. B.; Krall, J. A.; DeCock, J.; Zervantonakis, I. K.; Iannello, A.; Iwamoto, Y.; Cortez-Retamozo, V.; Kamm, R. D.; Pittet, M. J.; Raulet, D. H.; Weinberg, R. A.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5418-5133
dc.identifier.orcidhttps://orcid.org/0000-0002-7232-304X
dc.identifier.orcidhttps://orcid.org/0000-0002-0895-3557
mit.licenseOPEN_ACCESS_POLICYen_US


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