Breast Cancer-Derived Exosomes Reflect the Cell-of-Origin Phenotype

被引:106
作者
Wen, Shu Wen [1 ,2 ]
Lima, Luize G. [1 ]
Lobb, Richard J. [1 ]
Norris, Emma L. [3 ]
Hastie, Marcus L. [3 ]
Krumeich, Sophie [4 ]
Moller, Andreas [1 ]
机构
[1] QIMR Berghofer Med Res Inst, Tumour Microenvironm Lab, Herston, Qld 4006, Australia
[2] Monash Univ, Monash Med Ctr, Neuroinflammat Lab, Clayton, Vic 3800, Australia
[3] QIMR Berghofer Med Res Inst, Prot Discovery Ctr, Herston, Qld 4006, Australia
[4] QIMR Berghofer Med Res Inst, Oncol & Cellular Immunol, Herston, Qld 4006, Australia
基金
英国医学研究理事会;
关键词
breast cancer; epithelial-to-mesenchymal transition; exosomes; proteomic; TO-MESENCHYMAL TRANSITION; PROGENITOR CELLS; METASTASIS; MECHANISMS; EMT; EXPRESSION; VESICLES; PROTEOME; MODEL; STATE;
D O I
10.1002/pmic.201800180
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:9
相关论文
共 50 条
[1]   Intercellular transfer of the oncogenic receptor EGFrvIII by microvesicles derived from tumour cells [J].
Al-Nedawi, Khalid ;
Meehan, Brian ;
Micallef, Johann ;
Lhotak, Vladimir ;
May, Linda ;
Guha, Abhijit ;
Rak, Janusz .
NATURE CELL BIOLOGY, 2008, 10 (05) :619-U24
[2]   Conversion to stem-cell state in response to microenvironmental cues is regulated by balance between epithelial and mesenchymal features in lung cancer cells [J].
Andriani, Francesca ;
Bertolini, Giulia ;
Facchinetti, Federica ;
Baldoli, Erika ;
Moro, Massimo ;
Casalini, Patrizia ;
Caserini, Roberto ;
Milione, Massimo ;
Leone, Giorgia ;
Pelosi, Giuseppe ;
Pastorino, Ugo ;
Sozzi, Gabriella ;
Roz, Luca .
MOLECULAR ONCOLOGY, 2016, 10 (02) :253-271
[3]   EMT: 2016 [J].
Angela Nieto, M. ;
Huang, Ruby Yun-Ju ;
Jackson, Rebecca A. ;
Thiery, Jean Paul .
CELL, 2016, 166 (01) :21-45
[4]   Proteomic Analysis of Exosomes from Mutant KRAS Colon Cancer Cells Identifies Intercellular Transfer of Mutant KRAS [J].
Beckler, Michelle Demory ;
Higginbotham, James N. ;
Franklin, Jeffrey L. ;
Ham, Amy-Joan ;
Halvey, Patrick J. ;
Imasuen, Imade E. ;
Whitwell, Corbin ;
Li, Ming ;
Liebler, Daniel C. ;
Coffey, Robert J. .
MOLECULAR & CELLULAR PROTEOMICS, 2013, 12 (02) :343-355
[5]   Oncogenic Effects of High MAPK Activity in Colorectal Cancer Mark Progenitor Cells and Persist Irrespective of RAS Mutations [J].
Blaj, Cristina ;
Schmidt, Eva Marina ;
Lamprecht, Sebastian ;
Hermeking, Heiko ;
Jung, Andreas ;
Kirchner, Thomas ;
Horst, David .
CANCER RESEARCH, 2017, 77 (07) :1763-1774
[6]   Exosome release of β-catenin: a novel mechanism that antagonizes Wnt signaling [J].
Chairoungdua, Arthit ;
Smith, Danielle L. ;
Pochard, Pierre ;
Hull, Michael ;
Caplan, Michael J. .
JOURNAL OF CELL BIOLOGY, 2010, 190 (06) :1079-1091
[7]   Docetaxel-Resistance in Prostate Cancer: Evaluating Associated Phenotypic Changes and Potential for Resistance Transfer via Exosomes [J].
Corcoran, Claire ;
Rani, Sweta ;
O'Brien, Keith ;
O'Neill, Amanda ;
Prencipe, Maria ;
Sheikh, Rizwan ;
Webb, Glenn ;
McDermott, Ray ;
Watson, William ;
Crown, John ;
O'Driscoll, Lorraine .
PLOS ONE, 2012, 7 (12)
[8]   Pancreatic cancer exosomes initiate pre-metastatic niche formation in the liver [J].
Costa-Silva, Bruno ;
Aiello, Nicole M. ;
Ocean, Allyson J. ;
Singh, Swarnima ;
Zhang, Haiying ;
Thakur, Basant Kumar ;
Becker, Annette ;
Hoshino, Ayuko ;
Mark, Milica Tesic ;
Molina, Henrik ;
Xiang, Jenny ;
Zhang, Tuo ;
Theilen, Till-Martin ;
Garcia-Santos, Guillermo ;
Williams, Caitlin ;
Ararso, Yonathan ;
Huang, Yujie ;
Rodrigues, Goncalo ;
Shen, Tang-Long ;
Labori, Knut Jorgen ;
Lothe, Inger Marie Bowitz ;
Kure, Elm H. ;
Hernandez, Jonathan ;
Doussot, Alexandre ;
Ebbesen, Saya H. ;
Grandgenett, Paul M. ;
Hollingsworth, Michael A. ;
Jain, Maneesh ;
Mallya, Kavita ;
Batra, Surinder K. ;
Jarnagin, William R. ;
Schwartz, Robert E. ;
Matei, Irina ;
Peinado, Hector ;
Stanger, Ben Z. ;
Bromberg, Jacqueline ;
Lyden, David .
NATURE CELL BIOLOGY, 2015, 17 (06) :816-+
[9]   Andromeda: A Peptide Search Engine Integrated into the MaxQuant Environment [J].
Cox, Juergen ;
Neuhauser, Nadin ;
Michalski, Annette ;
Scheltema, Richard A. ;
Olsen, Jesper V. ;
Mann, Matthias .
JOURNAL OF PROTEOME RESEARCH, 2011, 10 (04) :1794-1805
[10]   MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification [J].
Cox, Juergen ;
Mann, Matthias .
NATURE BIOTECHNOLOGY, 2008, 26 (12) :1367-1372