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DC Field | Value | Language |
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dc.contributor.author | Moller A. | en |
dc.contributor.author | Wen S.W. | en |
dc.contributor.author | Lima L.G. | en |
dc.contributor.author | Lobb R.J. | en |
dc.contributor.author | Norris E.L. | en |
dc.contributor.author | Hastie M.L. | en |
dc.contributor.author | Krumeich S. | en |
dc.date.accessioned | 2021-05-14T12:03:44Z | en |
dc.date.available | 2021-05-14T12:03:44Z | en |
dc.date.copyright | 2019 | en |
dc.date.created | 20190429 | en |
dc.date.issued | 2019-04-29 | en |
dc.identifier.citation | Proteomics. 19 (8) (no pagination), 2019. Article Number: 1800180. Date of Publication: April 2019. | en |
dc.identifier.issn | 1615-9853 | en |
dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/35665 | en |
dc.description.abstract | A 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, Weinheim | en |
dc.language | English | en |
dc.language | en | en |
dc.publisher | Wiley-VCH Verlag (E-mail: info@wiley-vch.de) | en |
dc.relation.ispartof | Proteomics | en |
dc.title | Breast Cancer-Derived Exosomes Reflect the Cell-of-Origin Phenotype. | en |
dc.type | Article | en |
dc.identifier.doi | http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1002/pmic.201800180 | en |
dc.publisher.place | Germany | en |
dc.identifier.pubmedid | 30672117 [http://www.ncbi.nlm.nih.gov/pubmed/?term=30672117] | en |
dc.identifier.source | 626600908 | en |
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, Australia | en |
dc.description.address | A. Moller, Tumour Microenvironment Laboratory, QIMR Berghofer Medical Research Institute, Herston, QLD 4006, Australia. E-mail: andreas.moller@qimrberghofer.edu.au | en |
dc.description.publicationstatus | Embase | en |
dc.rights.statement | Copyright 2019 Elsevier B.V., All rights reserved. | en |
dc.subect.keywords | breast cancer epithelial-to-mesenchymal transition exosomes proteomic | en |
dc.identifier.authoremail | Moller A.; andreas.moller@qimrberghofer.edu.au | en |
dc.description.grant | Organization: *National Breast Cancer Foundation* Organization No: 501100001026 Country: Australia Organization: *National Health and Medical Research Council* Organization No: 501100000925 Country: Australia | en |
item.cerifentitytype | Publications | - |
item.fulltext | No Fulltext | - |
item.openairetype | Article | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
Appears in Collections: | Articles |
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