Recent advances on the role of tumor exosomes in immunosuppression and disease progression

被引:249
作者
Filipazzi, Paola [1 ]
Buerdek, Maja [1 ]
Villa, Antonello [2 ]
Rivoltini, Licia [1 ]
Huber, Veronica [1 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Unit Immunotherapy Human Tumors, I-20133 Milan, Italy
[2] Univ Milano Bicocca, CONSORZIO MIA Microscopy & Image Anal, I-20052 Monza, MI, Italy
关键词
Microvesicles; T cell apoptosis; Myeloid-derived suppressor cells; NK dysfunction; Cancer treatment; REGULATORY T-CELLS; ASCITES-DERIVED EXOSOMES; OVARIAN-CANCER PATIENTS; SUPPRESSOR-CELLS; FAS LIGAND; COLORECTAL-CANCER; MELANOMA PATIENTS; IMMUNE-RESPONSES; PROSTATE-CANCER; GROWTH-FACTORS;
D O I
10.1016/j.semcancer.2012.02.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Exosomes are endosomal-derived nanovesicles released by most cells types, including tumor cells, and principally involved in intercellular communication in physiology and disease. Tumor exosomes are gaining increasing interest in medicine and oncology as efficient tools for the delivery of defined signals. Representing the acellular replicas of tumor cells, they contain a great variety of bioactive molecules, such as proteins. RNA, miRNA and DNA. Their great ability to recirculate in body fluids and their structure allow them to transport their cargo to distant targets. Major studies have shown that tumor exosomes convey information not only between tumor cells but also to other cell types, including different immune cell components. There is increasing evidence that these nanovesicles may contribute to cancer progression by influencing different immune cell types, likely blunting specific T cell immunity and skewing innate immune cells toward a pro-tumorigenic phenotype. Because of this function and the additional property to deliver molecular signals modulating neoangiogenesis and stroma remodeling, tumor exosomes are believed to play a role in tumor progression by favoring metastatic niche onset. This review outlines the recent knowledge on immune suppressive mechanisms mediated by tumor exosomes. We will discuss our view on the role of these nanovesicular structures in cancer progression and how their presence could interfere with cancer therapy. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:342 / 349
页数:8
相关论文
共 110 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]   Microvesicles Messengers and mediators of tumor progression [J].
Al-Nedawi, Khalid ;
Meehan, Brian ;
Rak, Janusz .
CELL CYCLE, 2009, 8 (13) :2014-2018
[4]   FAS LIGAND MEDIATES ACTIVATION-INDUCED CELL-DEATH IN HUMAN T-LYMPHOCYTES [J].
ALDERSON, MR ;
TOUGH, TW ;
DAVISSMITH, T ;
BRADDY, S ;
FALK, B ;
SCHOOLEY, KA ;
GOODWIN, RG ;
SMITH, CA ;
RAMSDELL, F ;
LYNCH, DH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (01) :71-77
[5]   Malignant effusions and immunogenic tumour-derived exosomes [J].
Andre, F ;
Schartz, NEC ;
Movassagh, M ;
Flament, C ;
Pautier, P ;
Morice, P ;
Pomel, C ;
Lhomme, C ;
Escudier, B ;
Le Chevalier, T ;
Tursz, T ;
Amigorena, S ;
Raposo, G ;
Angevin, E ;
Zitvogel, L .
LANCET, 2002, 360 (9329) :295-305
[6]   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
[7]   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
[8]   Exosomal evasion of humoral immunotherapy in aggressive B-cell lymphoma modulated by ATP-binding cassette transporter A3 [J].
Aung, Thiha ;
Chapuy, Bjoern ;
Vogel, Daniel ;
Wenzel, Dirk ;
Oppermann, Martin ;
Lahmann, Marlen ;
Weinhage, Toni ;
Menck, Kerstin ;
Hupfeld, Timo ;
Koch, Raphael ;
Truemper, Lorenz ;
Wulf, Gerald G. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (37) :15336-15341
[9]   Tumour exosomes inhibit binding of tumour-reactive antibodies to tumour cells and reduce ADCC [J].
Battke, Christina ;
Ruiss, Romana ;
Welsch, Ulrich ;
Wimberger, Pauline ;
Lang, Stephan ;
Jochum, Simon ;
Zeidler, Reinhard .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2011, 60 (05) :639-648
[10]   TUMOR-DERIVED MICROVESICLES IN SERA OF PATIENTS WITH HEAD AND NECK CANCER AND THEIR ROLE IN TUMOR PROGRESSION [J].
Bergmann, Christoph ;
Strauss, Laura ;
Wieckowski, Eva ;
Czystowska, Malgorzata ;
Albers, Andreas ;
Wang, Yun ;
Zeidler, Reinhard ;
Lang, Stephan ;
Whiteside, Theresa L. .
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, 2009, 31 (03) :371-380