Extracellular vesicle transfer of cancer pathogenic components

被引:178
作者
Fujita, Yu [1 ]
Yoshioka, Yusuke [1 ]
Ochiya, Takahiro [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Mol & Cellular Med, Tokyo 104, Japan
关键词
Biomarker; exosome; extracellular vesicle; metastasis; microRNA; TUMOR-DERIVED EXOSOMES; INTERCELLULAR TRANSFER; DIAGNOSTIC BIOMARKERS; CIRCULATING MICRORNA; PREMETASTATIC NICHE; MESSENGER-RNAS; MICROVESICLES; CELLS; SERUM; MICROENVIRONMENT;
D O I
10.1111/cas.12896
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Extracellular vesicles (EV), known as exosomes and microvesicles, serve as versatile intercellular communication vehicles. Increasing evidence has shown that cancer cell-derived EV carry pathogenic components, such as proteins, messenger RNA (mRNA), microRNA (miRNA), DNA, lipids and transcriptional factors, that can mediate paracrine signaling in the tumor microenvironment. These data suggest that EV transfer of cancer pathogenic components enable long-distance crosstalk between cancer cells and distant organs, resulting in the promotion of the initial steps for pre-metastatic niche formation. Understanding the metastatic mechanisms through EV transfer may open up a new avenue for cancer therapeutic strategies. Furthermore, the circulating EV have also been of interest as a source for liquid biopsies. EV in body fluids provide a reliable source of miRNA and proteins for cancer biomarkers. The tumor-specific components in EV effectively provide various messages on the physiological and pathological status of cancer patients. Although many researchers are searching for EV biomarkers using miRNA microarrays and proteome analyses, the detection technology for circulating EV in body fluids has not yet reached the point of clinical application. In this review, we summarize recent findings regarding EV function, specifically in metastasis through the transfer of cancer pathogenic components. Furthermore, we highlight the potential of using circulating EV for cancer diagnosis.
引用
收藏
页码:385 / 390
页数:6
相关论文
共 80 条
[1]   miR-21 in the Extracellular Vesicles (EVs) of Cerebrospinal Fluid (CSF): A Platform for Glioblastoma Biomarker Development [J].
Akers, Johnny C. ;
Ramakrishnan, Valya ;
Kim, Ryan ;
Skog, Johan ;
Nakano, Ichiro ;
Pingle, Sandeep ;
Kalinina, Juliya ;
Hua, Wei ;
Kesari, Santosh ;
Mao, Ying ;
Breakefield, Xandra O. ;
Hochberg, Fred H. ;
Van Meir, Erwin G. ;
Carter, Bob S. ;
Chen, Clark C. .
PLOS ONE, 2013, 8 (10)
[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]   Exosomes serve as tumour markers for personalized diagnostics owing to their important role in cancer metastasis [J].
An, Taixue ;
Qin, Sihua ;
Xu, Yong ;
Tang, Yueting ;
Huang, Yiyao ;
Bo Situ ;
Inal, Jameel M. ;
Zheng, Lei .
JOURNAL OF EXTRACELLULAR VESICLES, 2015, 4
[4]   The blood-brain barrier: an overview - Structure, regulation, and clinical implications [J].
Ballabh, P ;
Braun, A ;
Nedergaard, M .
NEUROBIOLOGY OF DISEASE, 2004, 16 (01) :1-13
[5]   Changes in circulating microRNA levels associated with prostate cancer [J].
Bryant, R. J. ;
Pawlowski, T. ;
Catto, J. W. F. ;
Marsden, G. ;
Vessella, R. L. ;
Rhees, B. ;
Kuslich, C. ;
Visakorpi, T. ;
Hamdy, F. C. .
BRITISH JOURNAL OF CANCER, 2012, 106 (04) :768-774
[6]   microRNAs Derived from Circulating Exosomes as Noninvasive Biomarkers for Screening and Diagnosing Lung Cancer [J].
Cazzoli, Riccardo ;
Buttitta, Fiamma ;
Di Nicola, Marta ;
Malatesta, Sara ;
Marchetti, Antonio ;
Rom, William N. ;
Pass, Harvey I. .
JOURNAL OF THORACIC ONCOLOGY, 2013, 8 (09) :1156-1162
[7]   Exosome-Mediated Transfer of microRNAs Within the Tumor Microenvironment and Neuroblastoma Resistance to Chemotherapy [J].
Challagundla, Kishore B. ;
Wise, Petra M. ;
Neviani, Paolo ;
Chava, Haritha ;
Murtadha, Mariam ;
Xu, Tong ;
Kennedy, Rebekah ;
Ivan, Cristina ;
Zhang, Xinna ;
Vannini, Ivan ;
Fanini, Francesca ;
Amadori, Dino ;
Calin, George A. ;
Hadjidaniel, Michael ;
Shimada, Hiroyuki ;
Jong, Ambrose ;
Seeger, Robert C. ;
Asgharzadeh, Shahab ;
Goldkorn, Amir ;
Fabbri, Muller .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2015, 107 (07)
[8]   Human tumor-derived exosomes down-modulate NKG2D expression [J].
Clayton, Aled ;
Mitchell, J. Paul ;
Court, Jacquelyn ;
Linnane, Seamus ;
Mason, Malcolm D. ;
Tabi, Zsuzsanna .
JOURNAL OF IMMUNOLOGY, 2008, 180 (11) :7249-7258
[9]   Intracellular and Extracellular MicroRNAs in Breast Cancer [J].
Corcoran, Claire ;
Friel, Anne M. ;
Duffy, Michael J. ;
Crown, John ;
O'Driscoll, Lorraine .
CLINICAL CHEMISTRY, 2011, 57 (01) :18-32
[10]   Extracellular vesicles: biology and emerging therapeutic opportunities [J].
EL Andaloussi, Samir ;
Maeger, Imre ;
Breakefield, Xandra O. ;
Wood, Matthew J. A. .
NATURE REVIEWS DRUG DISCOVERY, 2013, 12 (05) :348-358