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dc.contributor.authorWeigert, Andreas
dc.contributor.authorZheng, Xiang
dc.contributor.authorNenzel, Alina
dc.contributor.authorTurkowski, Kati
dc.contributor.authorGünther, Stefan
dc.contributor.authorStrack, Elisabeth
dc.contributor.authorSirait-Fischer, Evelyn
dc.contributor.authorElwakeel, Eiman
dc.contributor.authorKur, Ivan M.
dc.contributor.authorNikam, Vandana S.
dc.contributor.authorValasarajan, Chanil
dc.contributor.authorWinter, Hauke
dc.contributor.authorWissgott, Alexander
dc.contributor.authorVoswinkel, Robert
dc.contributor.authorGrimminger, Friedrich
dc.contributor.authorBrüne, Bernhard
dc.contributor.authorSeeger, Werner
dc.contributor.authorPullamsetti, Soni Savai
dc.contributor.authorSavai, Rajkumar
dc.date.accessioned2023-04-13T12:38:30Z
dc.date.available2023-04-13T12:38:30Z
dc.date.issued2022
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/16210
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-15592
dc.description.abstractFibrocytes are bone marrow–derived monocytic cells implicated in wound healing. Here, we identify their role in lung cancer progression/ metastasis. Selective manipulation of fibrocytes in mouse lung tumor models documents the central role of fibrocytes in boosting niche features and enhancing metastasis. Importantly, lung cancer patients show increased number of circulating fibrocytes and marked fibrocyte accumulation in the cancer niche. Using double and triple co-culture systems with human lung cancer cells, fibrocytes, macrophages and endothelial cells, we substantiate the central features of cancer-supporting niche: enhanced cancer cell proliferation and migration, macrophage activation, augmented endothelial cell sprouting and fibrocyte maturation. Upregulation of endothelin and its receptors are noted, and dual endothelin receptor blockade suppresses all cancer-supportive phenotypic alterations via acting on fibrocyte interaction with the cancer niche. We thus provide evidence for a crucial role of fibrocytes in lung cancer progression and metastasis, suggesting targets for treatment strategies.
dc.language.isoen
dc.rightsNamensnennung 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddcddc:610
dc.titleFibrocytes boost tumor-supportive phenotypic switches in the lung cancer niche via the endothelin system
dc.typearticle
local.affiliationFB 11 - Medizin
local.source.spage1
local.source.epage21
local.source.journaltitleNature Communications
local.source.volume13
local.source.articlenumber6078
local.source.urihttps://doi.org/10.1038/s41467-022-33458-8


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