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dc.contributor.authorIrshad, S
dc.contributor.authorFlores-Borja, F
dc.contributor.authorLawler, K
dc.contributor.authorMonypenny, J
dc.contributor.authorEvans, R
dc.contributor.authorMale, V
dc.contributor.authorGordon, P
dc.contributor.authorCheung, A
dc.contributor.authorGazinska, P
dc.contributor.authorNoor, F
dc.contributor.authorWong, F
dc.contributor.authorGrigoriadis, A
dc.contributor.authorFruhwirth, GO
dc.contributor.authorBarber, PR
dc.contributor.authorWoodman, N
dc.contributor.authorPatel, D
dc.contributor.authorRodriguez-Justo, M
dc.contributor.authorOwen, J
dc.contributor.authorMartin, SG
dc.contributor.authorPinder, SE
dc.contributor.authorGillett, CE
dc.contributor.authorPoland, SP
dc.contributor.authorAmeer-Beg, S
dc.contributor.authorMcCaughan, F
dc.contributor.authorCarlin, LM
dc.contributor.authorHasan, U
dc.contributor.authorWithers, DR
dc.contributor.authorLane, P
dc.contributor.authorVojnovic, B
dc.contributor.authorQuezada, SA
dc.contributor.authorEllis, P
dc.contributor.authorTutt, ANJ
dc.contributor.authorNg, T
dc.date.accessioned2018-01-24T14:11:09Z
dc.date.accessioned2018-01-24T14:13:02Z
dc.date.issued2017-03-01
dc.identifier.citationCancer Research, 2017, 77 (5), pp. 1083 - 1096
dc.identifier.issn0008-5472
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1016
dc.identifier.eissn1538-7445
dc.identifier.doi10.1158/0008-5472.CAN-16-0598
dc.description.abstractCancer cells tend to metastasize first to tumor-draining lymph nodes, but the mechanisms mediating cancer cell invasion into the lymphatic vasculature remain little understood. Here, we show that in the human breast tumor microenvironment (TME), the presence of increased numbers of RORγt+ group 3 innate lymphoid cells (ILC3) correlates with an increased likelihood of lymph node metastasis. In a preclinical mouse model of breast cancer, CCL21-mediated recruitment of ILC3 to tumors stimulated the production of the CXCL13 by TME stromal cells, which in turn promoted ILC3-stromal interactions and production of the cancer cell motile factor RANKL. Depleting ILC3 or neutralizing CCL21, CXCL13, or RANKL was sufficient to decrease lymph node metastasis. Our findings establish a role for RORγt+ILC3 in promoting lymphatic metastasis by modulating the local chemokine milieu of cancer cells in the TME. Cancer Res; 77(5); 1083-96. ©2017 AACR.
dc.format.extent1083 - 1096
dc.languageeng
dc.language.isoeng
dc.publisherAMER ASSOC CANCER RESEARCH
dc.relation.replaceshttps://repository.icr.ac.uk/handle/internal/1015
dc.relation.replacesinternal/1015
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleRORγt+ Innate Lymphoid Cells Promote Lymph Node Metastasis of Breast Cancers.
dc.typeJournal Article
dcterms.dateAccepted2016-12-10
rioxxterms.versionofrecord10.1158/0008-5472.CAN-16-0598
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017-03-01
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCancer Research
pubs.issue5
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR
pubs.volume77
pubs.embargo.termsNot known
dc.contributor.icrauthorEvans, Rachel
dc.contributor.icrauthorTutt, Andrew


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