Platelets Extracellular Vesicles as Regulators of Cancer Progression-An Updated Perspective

被引:45
作者
Zmigrodzka, Magdalena [1 ]
Witkowska-Pilaszewicz, Olga [1 ]
Winnicka, Anna [1 ]
机构
[1] Warsaw Univ Life Sci WULS SGGW, Inst Vet Med, Dept Pathol & Vet Diagnost, Nowoursynowska 159c, PL-02787 Warsaw, Poland
关键词
extracellular vesicles; exosomes; ectosomes; neoplasia; MICROPARTICLES INDUCE ANGIOGENESIS; ACTIVATED PLATELETS; TISSUE-FACTOR; IN-VIVO; CIRCULATING MICROPARTICLES; MEMBRANE-VESICLES; GASTRIC-CANCER; MICROVESICLES; CELLS; EXOSOMES;
D O I
10.3390/ijms21155195
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
Extracellular vesicles (EVs) are a diverse group of membrane-bound structures secreted in physiological and pathological conditions by prokaryotic and eukaryotic cells. Their role in cell-to-cell communications has been discussed for more than two decades. More attention is paid to assess the impact of EVs in cancer. Numerous papers showed EVs as tumorigenesis regulators, by transferring their cargo molecules (miRNA, DNA, protein, cytokines, receptors, etc.) among cancer cells and cells in the tumor microenvironment. During platelet activation or apoptosis, platelet extracellular vesicles (PEVs) are formed. PEVs present a highly heterogeneous EVs population and are the most abundant EVs group in the circulatory system. The reason for the PEVs heterogeneity are their maternal activators, which is reflected on PEVs size and cargo. As PLTs role in cancer development is well-known, and PEVs are the most numerous EVs in blood, their feasible impact on cancer growth is strongly discussed. PEVs crosstalk could promote proliferation, change tumor microenvironment, favor metastasis formation. In many cases these functions were linked to the transfer into recipient cells specific cargo molecules from PEVs. The article reviews the PEVs biogenesis, cargo molecules, and their impact on the cancer progression.
引用
收藏
页码:1 / 18
页数:18
相关论文
共 118 条
[1]   Platelet-Derived Microvesicles: Multitalented Participants in Intercellular Communication [J].
Aatonen, Maria ;
Gronholm, Mikaela ;
Siljander, Pia R. -M. .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2012, 38 (01) :102-113
[2]   Isolation and characterization of platelet-derived extracellular vesicles [J].
Aatonen, Maria T. ;
Ohman, Tiina ;
Nyman, Tuula A. ;
Laitinen, Saara ;
Gronholm, Mikaela ;
Siljander, Pia R. -M. .
JOURNAL OF EXTRACELLULAR VESICLES, 2014, 3 (01)
[3]   Phagocytosis of platelet microvesicles and β2-glycoprotein I [J].
Abdel-Monem, Hanan ;
Dasgupta, Swapan K. ;
Le, Anhquyen ;
Prakasam, Anthony ;
Thiagarajan, Perumal .
THROMBOSIS AND HAEMOSTASIS, 2010, 104 (02) :335-341
[4]   Procoagulant profile in patients with immune thrombocytopenia [J].
Alvarez-Roman, Maria T. ;
Fernandez-Bello, Ihosvany ;
Jimenez-Yuste, Victor ;
Martin-Salces, Monica ;
Arias-Salgado, Elena G. ;
Rivas Pollmar, Maria I. ;
Justo Sanz, Raul ;
Butta, Nora V. .
BRITISH JOURNAL OF HAEMATOLOGY, 2016, 175 (05) :925-934
[5]   Platelet microparticle delivered microRNA-Let-7a promotes the angiogenic switch [J].
Anene, Chinedu ;
Graham, Anne M. ;
Boyne, James ;
Roberts, Wayne .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2018, 1864 (08) :2633-2643
[6]   Platelet-derived microparticles stimulate proliferation, survival, adhesion, and chemotaxis of hematopoietic cells [J].
Baj-Krzyworzeka, M ;
Majka, M ;
Pratico, D ;
Ratajczak, J ;
Vilaire, G ;
Kijowski, J ;
Reca, R ;
Janowska-Wieczorek, A ;
Ratajczak, MZ .
EXPERIMENTAL HEMATOLOGY, 2002, 30 (05) :450-459
[7]   Platelet and osteoclast β3 integrins are critical for bone metastasis [J].
Bakewell, SJ ;
Nestor, P ;
Prasad, S ;
Tomasson, MH ;
Dowland, N ;
Mehrotra, M ;
Scarborough, R ;
Kanter, J ;
Abe, K ;
Phillips, D ;
Weilbaecher, KN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (24) :14205-14210
[8]   Microparticles in Hematological Malignancies: Role in Coagulopathy and Tumor Pathogenesis [J].
Ball, Somedeb ;
Nugent, Kenneth .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2018, 355 (03) :207-214
[9]   Modulation of monocyte-endothelial cell interactions by platelet microparticles [J].
Barry, OP ;
Praticò, D ;
Savani, RC ;
FitzGerald, GA .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (01) :136-144
[10]   Arachidonic acid in platelet microparticles up-regulates cyclooxygenase-2-dependent prostaglandin formation via a protein kinase C mitogen-activated protein kinase-dependent pathway [J].
Barry, OP ;
Kazanietz, MG ;
Praticò, D ;
FitzGerald, GA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (11) :7545-7556