What is the blood concentration of extracellular vesicles? Implications for the use of extracellular vesicles as blood-borne biomarkers of cancer

被引:204
作者
Johnsen, Kasper Bendix [1 ]
Gudbergsson, Johann Mar [2 ]
Andresen, Thomas Lars [1 ]
Simonsen, Jens Baek [1 ]
机构
[1] Tech Univ Denmark, Dept Micro & Nanotechnol, Ctr Nanomed & Theranost, Lyngby, Denmark
[2] Aalborg Univ, Dept Hlth Sci & Technol, Lab Immunol & Canc Biol, Aalborg, Denmark
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2019年 / 1871卷 / 01期
关键词
NANOPARTICLE TRACKING ANALYSIS; PLASMA-DERIVED EXOSOMES; HUMAN-BODY FLUIDS; CIRCULATING EXOSOMES; DRUG-DELIVERY; PROTEOMIC DIVERSITY; MICRORNAS; SERUM; LIPOPROTEINS; THERAPEUTICS;
D O I
10.1016/j.bbcan.2018.11.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circulating biomarkers have a great potential in diagnosing cancer diseases at early stages, where curative treatment is a realistic possibility. In the recent years, using extracellular vesicles (EVs) derived from blood as biomarkers has gained widespread popularity, mainly because they are thought to be easy to isolate and carry a vast variety of biological cargos that can be analyzed for biomarker purposes. However, our current knowledge on the plasma EV concentration in normophysiological states is sparse. Here, we provide the very first mean estimate of the plasma EV concentration based on values obtained from a thorough literature review. The different estimates obtained from the literature are correlated to the isolation techniques used to obtain them, illustrating how some methodologies may over- or underestimate the plasma EV concentration. We also show that the estimated plasma EV concentration (approximately 10(10) EVs per mL) defines EVs as a minority population compared to other colloidal particles of the systemic circulation, namely the lipoproteins, which are known contaminants in EV isolates and carry biomarker molecules themselves. Lastly, we introduce the possibility of regarding EVs and lipoproteins as a continuum of lipid-containing particles to which biomarker molecules can be associated. Using such a holistic approach, increased strength of plasma-derived cancer biomarkers may soon be revealed.
引用
收藏
页码:109 / 116
页数:8
相关论文
共 95 条
[1]   Inflammaging and Frailty Status Do Not Result in an Increased Extracellular Vesicle Concentration in Circulation [J].
Alberro, Ainhoa ;
Saenz-Cuesta, Matias ;
Munoz-Culla, Maider ;
Mateo-Abad, Maider ;
Gonzalez, Esperanza ;
Carrasco-Garcia, Estefania ;
Arauzo-Bravo, Marcos J. ;
Matheu, Ander ;
Vergara, Itziar ;
Otaegui, David .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (07)
[2]   Bioinformatic analysis of endogenous and exogenous small RNAs on lipoproteins [J].
Allen, Ryan M. ;
Zhao, Shilin ;
Solano, Marisol A. Ramirez ;
Zhu, Wanying ;
Michell, Danielle L. ;
Wang, Yuhuan ;
Shyr, Yu ;
Sethupathy, Praveen ;
Linton, MacRae F. ;
Graf, Gregory A. ;
Sheng, Quanhu ;
Vickers, Kasey C. .
JOURNAL OF EXTRACELLULAR VESICLES, 2018, 7 (01)
[3]   High prevalence of mutant KRAS in circulating exosome-derived DNA from early-stage pancreatic cancer patients [J].
Allenson, K. ;
Castillo, J. ;
San Lucas, F. A. ;
Scelo, G. ;
Kim, D. U. ;
Bernard, V. ;
Davis, G. ;
Kumar, T. ;
Katz, M. ;
Overman, M. J. ;
Foretova, L. ;
Fabianova, E. ;
Holcatova, I. ;
Janout, V. ;
Meric-Bernstam, F. ;
Gascoyne, P. ;
Wistuba, I. ;
Varadhachary, G. ;
Brennan, P. ;
Hanash, S. ;
Li, D. ;
Maitra, A. ;
Alvarez, H. .
ANNALS OF ONCOLOGY, 2017, 28 (04) :741-747
[4]   Clinical utility of circulating non-coding RNAs - an update [J].
Anfossi, Simone ;
Babayan, Anna ;
Pantel, Klaus ;
Calin, George A. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2018, 15 (09) :541-563
[5]   Isolation of Exosomes from Blood Plasma: Qualitative and Quantitative Comparison of Ultracentrifugation and Size Exclusion Chromatography Methods [J].
Baranyai, Tamas ;
Herczeg, Kata ;
Onodi, Zsofia ;
Voszka, Istvan ;
Modos, Karoly ;
Marton, Nikolett ;
Nagy, Gyoergy ;
Maeger, Imre ;
Wood, Matthew J. ;
El Andaloussi, Samir ;
Palinkas, Zoltan ;
Kumar, Vikas ;
Nagy, Pater ;
Kittel, Agnes ;
Buzas, Edit Iren ;
Ferdinandy, Peter ;
Giricz, Zoltan .
PLOS ONE, 2015, 10 (12)
[6]   Single-step isolation of extracellular vesicles by size-exclusion chromatography [J].
Boing, Anita N. ;
van der Pol, Edwin ;
Grootemaat, Anita E. ;
Coumans, Frank A. W. ;
Sturk, Auguste ;
Nieuwland, Rienk .
JOURNAL OF EXTRACELLULAR VESICLES, 2014, 3 (01)
[7]  
Burillo E., 2016, SCI REP, V6, P1125, DOI [10.1038/srep3S477, DOI 10.1038/SREP3S477]
[8]   Evaluation of serum extracellular vesicle isolation methods for profiling miRNAs by next-generation sequencing [J].
Buschmann, Dominik ;
Kirchner, Benedikt ;
Hermann, Stefanie ;
Maerte, Melanie ;
Wurmser, Christine ;
Brandes, Florian ;
Kotschote, Stefan ;
Bonin, Michael ;
Steinlein, Ortrud K. ;
Pfaffl, Michael W. ;
Schelling, Gustav ;
Reithmair, Marlene .
JOURNAL OF EXTRACELLULAR VESICLES, 2018, 7 (01)
[9]   Exosome levels in human body fluids: A tumor marker by themselves? [J].
Cappello, Francesco ;
Logozzi, Mariantonia ;
Campanella, Claudia ;
Bavisotto, Celeste Caruso ;
Marcilla, Antonio ;
Properzi, Francesca ;
Fais, Stefano .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 96 :93-98
[10]   Reproducibility and efficiency of serum-derived exosome extraction methods [J].
Caradec, Josselin ;
Kharmate, Geetanjali ;
Hosseini-Beheshti, Elham ;
Adomat, Hans ;
Gleave, Martin ;
Guns, Emma .
CLINICAL BIOCHEMISTRY, 2014, 47 (13-14) :1286-1292