Implications and pitfalls for cancer diagnostics exploiting extracellular vesicles

被引:28
作者
Spilak, Ana [1 ]
Brachner, Andreas [1 ]
Kegler, Ulrike [1 ]
Neuhaus, Winfried [1 ]
Noehammer, Christa [1 ]
机构
[1] AIT Austrian Inst Technol GmbH, Ctr Hlth & Bioresources, Competence Unit Mol Diagnost, Giefinggasse 4, A-1210 Vienna, Austria
基金
欧盟地平线“2020”; 奥地利科学基金会;
关键词
Tumor marker; Biomarker; Exosomes; Oncology; Preventive screening; Therapy monitoring; miRNA; TISSUE FACTOR ACTIVITY; PROSTATE-CANCER; CIRCULATING EXOSOMES; SERUM EXOSOMES; BREAST-CANCER; HEPATOCELLULAR-CARCINOMA; CLINICAL-SIGNIFICANCE; POTENTIAL BIOMARKERS; COLORECTAL-CANCER; MELANOMA EXOSOMES;
D O I
10.1016/j.addr.2021.05.029
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Early detection of cancer in order to facilitate timely therapeutic interventions is an unsolved problem in today's clinical diagnostics. Tumors are detected so far mostly after pathological symptoms have emerged (usually already in progressed disease states), within preventive screenings, or occasionally as incidental finding. The emergence of extracellular vesicle (EV) analytics in combination with liquid biopsy sampling opened a plethora of new possibilities for the detection of tumors (and other diseases). This review gives an overview of the diversity of currently known EV species and the relevant cargo molecules representing potential biomarkers to detect, identify and characterize tumor cells. A number of molecules reported in recent years to be valuable targets for different aspects of cancer diagnostics, are presented. Furthermore, we discuss (technical) challenges and pitfalls related to the various potential applications (screening, diagnosis, prognosis, monitoring) of liquid biopsy based EV analytics, and give an outlook to possible future directions of this emerging field in oncology. (c) 2021 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页数:18
相关论文
共 205 条
[1]  
Ahmed MK., 2017, J ONCOL SCI, V3, P5, DOI DOI 10.1016/J.JONS.2017.01.001
[2]   Circulating melanoma exosomes as diagnostic and prognosis biomarkers [J].
Alegre, Estibaliz ;
Zubiri, Leyre ;
Luis Perez-Gracia, Jose ;
Gonzalez-Cao, Maria ;
Soria, Lourdes ;
Martin-Algarra, Salvador ;
Gonzalez, Alvaro .
CLINICA CHIMICA ACTA, 2016, 454 :28-32
[3]   Clinical Applications of Circulating Tumor Cells and Circulating Tumor DNA as Liquid Biopsy [J].
Alix-Panabieres, Catherine ;
Pantel, Klaus .
CANCER DISCOVERY, 2016, 6 (05) :479-491
[4]   Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases [J].
Allard, WJ ;
Matera, J ;
Miller, MC ;
Repollet, M ;
Connelly, MC ;
Rao, C ;
Tibbe, AGJ ;
Uhr, JW ;
Terstappen, LWMM .
CLINICAL CANCER RESEARCH, 2004, 10 (20) :6897-6904
[5]   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
[6]   Urinary Exosomes as a Source of Kidney Dysfunction Biomarker in Renal Transplantation [J].
Alvarez, S. ;
Suazo, C. ;
Boltansky, A. ;
Ursu, M. ;
Carvajal, D. ;
Innocenti, G. ;
Vukusich, A. ;
Hurtado, M. ;
Villanueva, S. ;
Carreno, J. E. ;
Rogelio, A. ;
Irarrazabal, C. E. .
TRANSPLANTATION PROCEEDINGS, 2013, 45 (10) :3719-3723
[7]  
[Anonymous], 2015, Worldwide cancer statistics
[8]  
[Anonymous], 2015, Pancreatic cancer statistics
[9]  
[Anonymous], SCREEN VAR CANC
[10]   Blood-Derived Biomarkers of Diagnosis, Prognosis and Therapy Response in Prostate Cancer Patients [J].
Balazs, Katalin ;
Antal, Lilla ;
Safrany, Geza ;
Lumniczky, Katalin .
JOURNAL OF PERSONALIZED MEDICINE, 2021, 11 (04)