Please use this identifier to cite or link to this item:
https://hdl.handle.net/11055/156
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Le, Caroline P | - |
dc.contributor.author | Nowell, Cameron J | - |
dc.contributor.author | Kim-Fuchs, Corina | - |
dc.contributor.author | Botteri, Edoardo | - |
dc.contributor.author | Hiller, JG | - |
dc.contributor.author | Ismail, H | - |
dc.contributor.author | Pimentel, Matthew A | - |
dc.contributor.author | Chai, Ming G | - |
dc.contributor.author | Karnezis, Tara | - |
dc.contributor.author | Rotmensz, Nicole | - |
dc.contributor.author | Renne, Giuseppe | - |
dc.contributor.author | Gandini, Sara | - |
dc.contributor.author | Pouton, Colin W | - |
dc.contributor.author | Ferrar, Davide | - |
dc.contributor.author | Möller, Andreas | - |
dc.contributor.author | Stacker, Steven A | - |
dc.contributor.author | Sloan, Erica K | - |
dc.date | 2016 | - |
dc.date.accessioned | 2018-02-22T03:00:39Z | - |
dc.date.available | 2018-02-22T03:00:39Z | - |
dc.date.issued | 2016-03-01 | - |
dc.identifier.citation | Nature communications 2016-03-01; 7: 10634 | - |
dc.identifier.uri | http://hdl.handle.net/11055/156 | - |
dc.description.abstract | Chronic stress induces signalling from the sympathetic nervous system (SNS) and drives cancer progression, although the pathways of tumour cell dissemination are unclear. Here we show that chronic stress restructures lymphatic networks within and around tumours to provide pathways for tumour cell escape. We show that VEGFC derived from tumour cells is required for stress to induce lymphatic remodelling and that this depends on COX2 inflammatory signalling from macrophages. Pharmacological inhibition of SNS signalling blocks the effect of chronic stress on lymphatic remodelling in vivo and reduces lymphatic metastasis in preclinical cancer models and in patients with breast cancer. These findings reveal unanticipated communication between stress-induced neural signalling and inflammation, which regulates tumour lymphatic architecture and lymphogenous tumour cell dissemination. These findings suggest that limiting the effects of SNS signalling to prevent tumour cell dissemination through lymphatic routes may provide a strategy to improve cancer outcomes. | - |
dc.language.iso | eng | - |
dc.subject.mesh | Animals | - |
dc.subject.mesh | Breast Neoplasms | - |
dc.subject.mesh | Cell Line | - |
dc.subject.mesh | Chronic Disease | - |
dc.subject.mesh | Cyclooxygenase 2 | - |
dc.subject.mesh | Female | - |
dc.subject.mesh | Gene Expression Regulation, Neoplastic | - |
dc.subject.mesh | Lymphatic System | - |
dc.subject.mesh | Mice | - |
dc.subject.mesh | Mice, Inbred BALB C | - |
dc.subject.mesh | Mice, Nude | - |
dc.subject.mesh | Neoplasms | - |
dc.subject.mesh | Neoplasms, Experimental | - |
dc.subject.mesh | Signal Transduction | - |
dc.subject.mesh | Stress, Physiological | - |
dc.subject.mesh | Vascular Endothelial Growth Factor C | - |
dc.title | Chronic stress in mice remodels lymph vasculature to promote tumour cell dissemination. | - |
dc.type | Journal Article | - |
dc.type | Research Support, N.I.H., Extramural | - |
dc.type | Research Support, Non-U.S. Gov't | - |
dc.identifier.journaltitle | Nature communications | - |
dc.identifier.doi | 10.1038/ncomms10634 | - |
dc.description.pubmeduri | https://www.ncbi.nlm.nih.gov/pubmed/26925549 | - |
dc.identifier.pubmedid | 26925549 | - |
dc.ispartof.anzcaresearchfoundation | Yes | - |
item.cerifentitytype | Publications | - |
item.cerifentitytype | Publications | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Journal Article | - |
item.openairetype | Research Support, N.I.H., Extramural | - |
item.openairetype | Research Support, Non-U.S. Gov't | - |
item.fulltext | No Fulltext | - |
Appears in Collections: | Scholarly and Clinical |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.