The roles of extracellular vesicles in cancer biology: Toward the development of novel cancer biomarkers

被引:154
作者
Katsuda, Takeshi [1 ]
Kosaka, Nobuyoshi [1 ]
Ochiya, Takahiro [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Mol & Cellular Med, Tokyo 1040045, Japan
基金
日本学术振兴会;
关键词
Biomarker; Biomedicine; Cancer; Diagnosis; Exosome; Microvesicle; MESENCHYMAL STEM-CELLS; TUMOR-DERIVED EXOSOMES; BONE-MARROW; INTERCELLULAR TRANSFER; LYMPHOCYTE-RESPONSES; CIRCULATING MICRORNA; TRANSFERRIN RECEPTOR; PROTEOMICS ANALYSIS; MICROVESICLES; SECRETION;
D O I
10.1002/pmic.201300389
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Recent important progress in cancer biology was the identification of the significant roles played by extracellular vesicles (EVs). EVs are secreted by a variety of mammalian cell types and have been revealed to play important roles in intercellular communications. EVs serve as unique communication vehicles in many ways. First, unlike cytokine signaling, EVs enable transportation not only of proteins, but also of nucleic acids, including mRNAs and microRNAs. Recent reports showing the functionality of these nucleic acids in the recipient cells have opened up a new avenue of cell-to-cell communication research. Second, EVs have been revealed to transport membrane components including receptors, such as epithelial growth factor receptor. These findings have provided significant insights into understanding the molecular mechanisms of cancer development. Third, EVs protect their contents from clearance by degrading enzymes present in the extracellular space, which allows for remote transportation of the contents, even between organs. This concept is highlighted by recent reports that suggest the deep involvement of cancer cell derived EVs in metastasis. From these points of view, we will summarize recent studies on the relevance of EVs in cancer biology. We will also highlight the possibility of novel diagnostic technologies using circulating EVs in body fluid.
引用
收藏
页码:412 / 425
页数:14
相关论文
共 142 条
[1]
Tumor exosomes expressing Fas ligand mediate CD8+ T-cell apoptosis [J].
Abusamra, AJ ;
Zhong, ZH ;
Zheng, XF ;
Li, M ;
Ichim, TE ;
Chin, JL ;
Min, WP .
BLOOD CELLS MOLECULES AND DISEASES, 2005, 35 (02) :169-173
[2]
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
[3]
Endothelial expression of autocrine VEGF upon the uptake of tumor-derived microvesicles containing oncogenic EGFR [J].
Al-Nedawi, Khalid ;
Meehan, Brian ;
Kerbel, Robert S. ;
Allison, Anthony C. ;
Rak, Janusz .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (10) :3794-3799
[4]
Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes [J].
Alvarez-Erviti, Lydia ;
Seow, Yiqi ;
Yin, HaiFang ;
Betts, Corinne ;
Lakhal, Samira ;
Wood, Matthew J. A. .
NATURE BIOTECHNOLOGY, 2011, 29 (04) :341-U179
[5]
Induction of lymphocyte apoptosis by tumor cell secretion of FasL-bearing microvesicles [J].
Andreola, G ;
Rivoltini, L ;
Castelli, C ;
Huber, V ;
Perego, P ;
Deho, P ;
Squarcina, P ;
Accornero, P ;
Lozupone, F ;
Lugini, L ;
Stringaro, A ;
Molinari, A ;
Arancia, G ;
Gentile, M ;
Parmiani, G ;
Fais, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (10) :1303-1316
[6]
Natural Killer Cell Cytotoxicity Is Suppressed by Exposure to the Human NKG2D Ligand MICA*008 That Is Shed by Tumor Cells in Exosomes [J].
Ashiru, Omodele ;
Boutet, Philippe ;
Fernandez-Messina, Lola ;
Agueera-Gonzalez, Sonia ;
Skepper, Jeremy N. ;
Vales-Gomez, Mar ;
Reyburn, Hugh T. .
CANCER RESEARCH, 2010, 70 (02) :481-489
[7]
AN ELECTRON MICROSCOPE STUDY OF MEGACARYOCYTE OF RAT BONE MARROW .1. DEVELOPMENT OF DEMARCATION MEMBRANE SYSTEM AND PLATELET SURFACE COAT [J].
BEHNKE, O .
JOURNAL OF ULTRASTRUCTURE RESEARCH, 1968, 24 (5-6) :412-+
[8]
Signaling of the tissue factor coagulation pathway in angiogenesis and cancer [J].
Belting, M ;
Ahamed, J ;
Ruf, W .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (08) :1545-1550
[9]
Therapeutic potential of mesenchymal stem cell-derived microvesicles [J].
Biancone, Luigi ;
Bruno, Stefania ;
Deregibus, Maria Chiara ;
Tetta, Ciro ;
Camussi, Giovanni .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2012, 27 (08) :3037-3042
[10]
Predominant expression of mutant EGFR (EGFRvIII) is rare in primary glioblastomas [J].
Biernat, W ;
Huang, H ;
Yokoo, H ;
Kleihues, P ;
Ohgaki, H .
BRAIN PATHOLOGY, 2004, 14 (02) :131-136