Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16827
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dc.contributor.authorMouchemore, Kellie A-
dc.contributor.authorAnderson, Robin L-
dc.contributor.authorHamilton, John A-
dc.date2017-08-21-
dc.date.accessioned2017-08-31T05:39:04Z-
dc.date.available2017-08-31T05:39:04Z-
dc.date.issued2017-08-21-
dc.identifier.citationThe FEBS Journal 2017; 285(4): 665-679en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16827-
dc.description.abstractEvidence is mounting for a role for neutrophils in breast cancer progression to metastasis. However, the role of G-CSF in neutrophil biology in a cancer setting remains to be defined. Herein we discuss the most recent clinical and experimental evidence for neutrophils and G-CSF in the promotion of metastasis, demonstrating a potential mechanistic link between them. Understanding this link is imperative both for the development of diagnostic tests and for therapies targeting neutrophils to improve the treatment of breast cancer patients with, or at risk of developing metastatic disease. Since a high neutrophil to lymphocyte ratio in patients predicts poor outcome, while mild neutropenia predicts an improved outcome, we urge caution in the use of G-CSF in neutrophil recovery following chemotherapy as there is increasing evidence in preclinical models that G-CSF can promote metastasis.en_US
dc.subjectBreast canceren_US
dc.subjectG-CSFen_US
dc.subjectMetastasisen_US
dc.subjectNeutrophil extracellular trapsen_US
dc.subjectNeutrophilsen_US
dc.subjectTherapyen_US
dc.titleNeutrophils, G-CSF and their contribution to breast cancer metastasisen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThe FEBS Journalen_US
dc.identifier.affiliationDepartment of Biochemistry and Molecular Biology, Monash University, Clayton, Victoria, Australiaen_US
dc.identifier.affiliationSir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationOlivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationLa Trobe University School of Cancer Medicine, Bundoora, Victoria, Australiaen_US
dc.identifier.affiliationArthritis and Inflammation Research Centre, Department of Medicine, The University of Melbourne, Royal Melbourne Hospital, Parkville, Victoria, Australiaen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28834401en_US
dc.identifier.doi10.1111/febs.14206en_US
dc.type.contentTexten_US
dc.type.austinJournal Articleen_US
local.name.researcherAnderson, Robin L
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
Appears in Collections:Journal articles
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