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dc.contributor.authorBarrow-McGee, R
dc.contributor.authorProcter, J
dc.contributor.authorOwen, J
dc.contributor.authorWoodman, N
dc.contributor.authorLombardelli, C
dc.contributor.authorKothari, A
dc.contributor.authorKovacs, T
dc.contributor.authorDouek, M
dc.contributor.authorGeorge, S
dc.contributor.authorBarry, PA
dc.contributor.authorRamsey, K
dc.contributor.authorGibson, A
dc.contributor.authorBuus, R
dc.contributor.authorHolgersen, E
dc.contributor.authorNatrajan, R
dc.contributor.authorHaider, S
dc.contributor.authorShattock, MJ
dc.contributor.authorGillett, C
dc.contributor.authorTutt, AN
dc.contributor.authorPinder, SE
dc.contributor.authorNaidoo, K
dc.date.accessioned2019-12-06T14:57:40Z
dc.date.issued2020-03-01
dc.identifier.citationThe Journal of pathology, 2020, 250 (3), pp. 262 - 274
dc.identifier.issn0022-3417
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3445
dc.identifier.eissn1096-9896
dc.identifier.doi10.1002/path.5367
dc.description.abstractUnderstanding how breast cancer (BC) grows in axillary lymph nodes (ALNs), and refining how therapies might halt that process, is clinically important. However, modelling the complex ALN microenvironment is difficult, and no human models exist at present. We harvested ALNs from ten BC patients, and perfused them at 37 °C ex vivo for up to 24 h. Controlled autologous testing showed that ALNs remain viable after 24 h of ex vivo perfusion: haematoxylin and eosin-stained histological appearance and proliferation (by Ki67 immunohistochemistry) did not change significantly over time for any perfused ALN compared with a control from time-point zero. Furthermore, targeted gene expression analysis (NanoString PanCancer IO360 panel) showed that only 21/750 genes were differentially expressed between control and perfused ALNs (|log2 FC| > 1 and q < 0.1): none were involved in apoptosis and metabolism, but rather all 21 genes were involved in immune function and angiogenesis. During perfusion, tissue acid-base balance remained stable. Interestingly, the flow rate increased (p < 0.001) in cancer-replaced (i.e. metastasis occupied more than 90% of the surface area on multiple levels) compared to cancer-free nodes (i.e. nodes with no metastasis on multiple sections). CXCL11 transcripts were significantly more abundant in cancer-replaced nodes, while CXCL12 transcripts were significantly more abundant in cancer-free nodes. These cytokines were also detected in the circulating perfusate. Monoclonal antibodies (nivolumab and trastuzumab) were administered into a further three ALNs to confirm perfusion efficacy. These drugs saturated the nodes; nivolumab even induced cancer cell death. Normothermic ALN perfusion is not only feasible but sustains the tumour microenvironment ex vivo for scientific investigation. This model could facilitate the identification of actionable immuno-oncology targets. © 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
dc.formatPrint-Electronic
dc.format.extent262 - 274
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectLymph Nodes
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectLymphatic Metastasis
dc.subjectFeasibility Studies
dc.subjectPerfusion
dc.subjectMiddle Aged
dc.subjectFemale
dc.titleReal-time ex vivo perfusion of human lymph nodes invaded by cancer (REPLICANT): a feasibility study.
dc.typeJournal Article
dcterms.dateAccepted2019-11-18
rioxxterms.versionofrecord10.1002/path.5367
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2020-03
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfThe Journal of pathology
pubs.issue3
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/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Functional Genomics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Target Validation and DNA Damage Response
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Functional Genomics
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/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Functional Genomics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Target Validation and DNA Damage Response
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Functional Genomics
pubs.publication-statusPublished
pubs.volume250
pubs.embargo.termsNot known
icr.researchteamTarget Validation and DNA Damage Response
icr.researchteamFunctional Genomics
dc.contributor.icrauthorBuus, Richard
dc.contributor.icrauthorNatrajan, Rachael
dc.contributor.icrauthorHaider, Syed
dc.contributor.icrauthorTutt, Andrew
dc.contributor.icrauthorNaidoo, Kalnisha


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https://creativecommons.org/licenses/by/4.0
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0