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

被引:184
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
    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
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (07):
  • [2] Bioinformatic analysis of endogenous and exogenous small RNAs on lipoproteins
    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.
    [J]. JOURNAL OF EXTRACELLULAR VESICLES, 2018, 7 (01)
  • [3] High prevalence of mutant KRAS in circulating exosome-derived DNA from early-stage pancreatic cancer patients
    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.
    [J]. ANNALS OF ONCOLOGY, 2017, 28 (04) : 741 - 747
  • [4] Clinical utility of circulating non-coding RNAs - an update
    Anfossi, Simone
    Babayan, Anna
    Pantel, Klaus
    Calin, George A.
    [J]. 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
    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
    [J]. PLOS ONE, 2015, 10 (12):
  • [6] Single-step isolation of extracellular vesicles by size-exclusion chromatography
    Boing, Anita N.
    van der Pol, Edwin
    Grootemaat, Anita E.
    Coumans, Frank A. W.
    Sturk, Auguste
    Nieuwland, Rienk
    [J]. 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
    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
    [J]. JOURNAL OF EXTRACELLULAR VESICLES, 2018, 7 (01)
  • [9] Exosome levels in human body fluids: A tumor marker by themselves?
    Cappello, Francesco
    Logozzi, Mariantonia
    Campanella, Claudia
    Bavisotto, Celeste Caruso
    Marcilla, Antonio
    Properzi, Francesca
    Fais, Stefano
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 96 : 93 - 98
  • [10] Reproducibility and efficiency of serum-derived exosome extraction methods
    Caradec, Josselin
    Kharmate, Geetanjali
    Hosseini-Beheshti, Elham
    Adomat, Hans
    Gleave, Martin
    Guns, Emma
    [J]. CLINICAL BIOCHEMISTRY, 2014, 47 (13-14) : 1286 - 1292