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Molecular characterization of exosome-like vesicles from breast cancer cells
BACKGROUND: Membrane vesicles released by neoplastic cells into extracellular medium contain potential of carrying arrays of oncogenic molecules including proteins and microRNAs (miRNA). Extracellular (exosome-like) vesicles play a major role in cell-to-cell communication. Thus, the characterization...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936808/ https://www.ncbi.nlm.nih.gov/pubmed/24468161 http://dx.doi.org/10.1186/1471-2407-14-44 |
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author | Kruger, Stefan Elmageed, Zakaria Y Abd Hawke, David H Wörner, Philipp M Jansen, David A Abdel-Mageed, Asim B Alt, Eckhard U Izadpanah, Reza |
author_facet | Kruger, Stefan Elmageed, Zakaria Y Abd Hawke, David H Wörner, Philipp M Jansen, David A Abdel-Mageed, Asim B Alt, Eckhard U Izadpanah, Reza |
author_sort | Kruger, Stefan |
collection | PubMed |
description | BACKGROUND: Membrane vesicles released by neoplastic cells into extracellular medium contain potential of carrying arrays of oncogenic molecules including proteins and microRNAs (miRNA). Extracellular (exosome-like) vesicles play a major role in cell-to-cell communication. Thus, the characterization of proteins and miRNAs of exosome-like vesicles is imperative in clarifying intercellular signaling as well as identifying disease markers. METHODS: Exosome-like vesicles were isolated using gradient centrifugation from MCF-7 and MDA-MB 231 cultures. Proteomic profiling of vesicles using liquid chromatography-mass spectrometry (LC-MS/MS) revealed different protein profiles of exosome-like vesicles derived from MCF-7 cells (MCF-Exo) than those from MDA-MB 231 cells (MDA-Exo). RESULTS: The protein database search has identified 88 proteins in MDA-Exo and 59 proteins from MCF-Exo. Analysis showed that among all, 27 proteins were common between the two exosome-like vesicle types. Additionally, MDA-Exo contains a higher amount of matrix-metalloproteinases, which might be linked to the enhanced metastatic property of MDA-MB 231 cells. In addition, microarray analysis identified several oncogenic miRNA between the two types vesicles. CONCLUSIONS: Identification of the oncogenic factors in exosome-like vesicles is important since such vesicles could convey signals to non-malignant cells and could have an implication in tumor progression and metastasis. |
format | Online Article Text |
id | pubmed-3936808 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39368082014-02-28 Molecular characterization of exosome-like vesicles from breast cancer cells Kruger, Stefan Elmageed, Zakaria Y Abd Hawke, David H Wörner, Philipp M Jansen, David A Abdel-Mageed, Asim B Alt, Eckhard U Izadpanah, Reza BMC Cancer Research Article BACKGROUND: Membrane vesicles released by neoplastic cells into extracellular medium contain potential of carrying arrays of oncogenic molecules including proteins and microRNAs (miRNA). Extracellular (exosome-like) vesicles play a major role in cell-to-cell communication. Thus, the characterization of proteins and miRNAs of exosome-like vesicles is imperative in clarifying intercellular signaling as well as identifying disease markers. METHODS: Exosome-like vesicles were isolated using gradient centrifugation from MCF-7 and MDA-MB 231 cultures. Proteomic profiling of vesicles using liquid chromatography-mass spectrometry (LC-MS/MS) revealed different protein profiles of exosome-like vesicles derived from MCF-7 cells (MCF-Exo) than those from MDA-MB 231 cells (MDA-Exo). RESULTS: The protein database search has identified 88 proteins in MDA-Exo and 59 proteins from MCF-Exo. Analysis showed that among all, 27 proteins were common between the two exosome-like vesicle types. Additionally, MDA-Exo contains a higher amount of matrix-metalloproteinases, which might be linked to the enhanced metastatic property of MDA-MB 231 cells. In addition, microarray analysis identified several oncogenic miRNA between the two types vesicles. CONCLUSIONS: Identification of the oncogenic factors in exosome-like vesicles is important since such vesicles could convey signals to non-malignant cells and could have an implication in tumor progression and metastasis. BioMed Central 2014-01-27 /pmc/articles/PMC3936808/ /pubmed/24468161 http://dx.doi.org/10.1186/1471-2407-14-44 Text en Copyright © 2014 Kruger et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kruger, Stefan Elmageed, Zakaria Y Abd Hawke, David H Wörner, Philipp M Jansen, David A Abdel-Mageed, Asim B Alt, Eckhard U Izadpanah, Reza Molecular characterization of exosome-like vesicles from breast cancer cells |
title | Molecular characterization of exosome-like vesicles from breast cancer cells |
title_full | Molecular characterization of exosome-like vesicles from breast cancer cells |
title_fullStr | Molecular characterization of exosome-like vesicles from breast cancer cells |
title_full_unstemmed | Molecular characterization of exosome-like vesicles from breast cancer cells |
title_short | Molecular characterization of exosome-like vesicles from breast cancer cells |
title_sort | molecular characterization of exosome-like vesicles from breast cancer cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936808/ https://www.ncbi.nlm.nih.gov/pubmed/24468161 http://dx.doi.org/10.1186/1471-2407-14-44 |
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