Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/35665
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dc.contributor.authorMoller A.en
dc.contributor.authorWen S.W.en
dc.contributor.authorLima L.G.en
dc.contributor.authorLobb R.J.en
dc.contributor.authorNorris E.L.en
dc.contributor.authorHastie M.L.en
dc.contributor.authorKrumeich S.en
dc.date.accessioned2021-05-14T12:03:44Zen
dc.date.available2021-05-14T12:03:44Zen
dc.date.copyright2019en
dc.date.created20190429en
dc.date.issued2019-04-29en
dc.identifier.citationProteomics. 19 (8) (no pagination), 2019. Article Number: 1800180. Date of Publication: April 2019.en
dc.identifier.issn1615-9853en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/35665en
dc.description.abstractA manner in which cells can communicate with each other is via secreted nanoparticles termed exosomes. These vesicles contain lipids, nucleic acids, and proteins, and are said to reflect the cell-of-origin. However, for the exosomal protein content, there is limited evidence in the literature to verify this statement. Here, proteomic assessment combined with pathway-enrichment analysis is used to demonstrate that the protein cargo of exosomes reflects the epithelial/mesenchymal phenotype of secreting breast cancer cells. Given that epithelial-mesenchymal plasticity is known to implicate various stages of cancer progression, the results suggest that breast cancer subtypes with distinct epithelial and mesenchymal phenotypes may be distinguished by directly assessing the protein content of exosomes. Additionally, the work is a substantial step toward verifying the statement that cell-derived exosomes reflect the phenotype of the cells-of-origin.Copyright © 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheimen
dc.languageEnglishen
dc.languageenen
dc.publisherWiley-VCH Verlag (E-mail: info@wiley-vch.de)en
dc.relation.ispartofProteomicsen
dc.titleBreast Cancer-Derived Exosomes Reflect the Cell-of-Origin Phenotype.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1002/pmic.201800180en
dc.publisher.placeGermanyen
dc.identifier.pubmedid30672117 [http://www.ncbi.nlm.nih.gov/pubmed/?term=30672117]en
dc.identifier.source626600908en
dc.identifier.institution(Wen, Lima, Lobb, Moller) Tumour Microenvironment Laboratory, QIMR Berghofer Medical Research Institute, Herston, QLD 4006, Australia (Wen) Neuroinflammation Laboratory, Monash University, Monash Medical Centre, VIC 3800, Australia (Norris, Hastie) Protein Discovery Centre, QIMR Berghofer Medical Research Institute, Herston, QLD 4006, Australia (Krumeich) Oncology and Cellular Immunology, QIMR Berghofer Medical Research Institute, Herston, QLD 4006, Australiaen
dc.description.addressA. Moller, Tumour Microenvironment Laboratory, QIMR Berghofer Medical Research Institute, Herston, QLD 4006, Australia. E-mail: andreas.moller@qimrberghofer.edu.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
dc.subect.keywordsbreast cancer epithelial-to-mesenchymal transition exosomes proteomicen
dc.identifier.authoremailMoller A.; andreas.moller@qimrberghofer.edu.auen
dc.description.grantOrganization: *National Breast Cancer Foundation* Organization No: 501100001026 Country: Australia Organization: *National Health and Medical Research Council* Organization No: 501100000925 Country: Australiaen
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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