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Proteomic Profiling of Extracellular Vesicles Allows for Human Breast Cancer Subtyping

Overview
Journal Commun Biol
Specialty Biology
Date 2019 Sep 12
PMID 31508500
Citations 113
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Abstract

Extracellular vesicles (EVs) are a potential source of disease-associated biomarkers for diagnosis. In breast cancer, comprehensive analyses of EVs could yield robust and reliable subtype-specific biomarkers that are still critically needed to improve diagnostic routines and clinical outcome. Here, we show that proteome profiles of EVs secreted by different breast cancer cell lines are highly indicative of their respective molecular subtypes, even more so than the proteome changes within the cancer cells. Moreover, we detected molecular evidence for subtype-specific biological processes and molecular pathways, hyperphosphorylated receptors and kinases in connection with the disease, and compiled a set of protein signatures that closely reflect the associated clinical pathophysiology. These unique features revealed in our work, replicated in clinical material, collectively demonstrate the potential of secreted EVs to differentiate between breast cancer subtypes and show the prospect of their use as non-invasive liquid biopsies for diagnosis and management of breast cancer patients.

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References
1.
Baietti M, Zhang Z, Mortier E, Melchior A, Degeest G, Geeraerts A . Syndecan-syntenin-ALIX regulates the biogenesis of exosomes. Nat Cell Biol. 2012; 14(7):677-85. DOI: 10.1038/ncb2502. View

2.
Marcotte R, Zhou L, Kim H, Roskelly C, Muller W . c-Src associates with ErbB2 through an interaction between catalytic domains and confers enhanced transforming potential. Mol Cell Biol. 2009; 29(21):5858-71. PMC: 2772728. DOI: 10.1128/MCB.01731-08. View

3.
Thery C, Witwer K, Aikawa E, Alcaraz M, Anderson J, Andriantsitohaina R . Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines. J Extracell Vesicles. 2019; 7(1):1535750. PMC: 6322352. DOI: 10.1080/20013078.2018.1535750. View

4.
Simpson R, Kalra H, Mathivanan S . ExoCarta as a resource for exosomal research. J Extracell Vesicles. 2013; 1. PMC: 3760644. DOI: 10.3402/jev.v1i0.18374. View

5.
Tyanova S, Temu T, Sinitcyn P, Carlson A, Hein M, Geiger T . The Perseus computational platform for comprehensive analysis of (prote)omics data. Nat Methods. 2016; 13(9):731-40. DOI: 10.1038/nmeth.3901. View