Microparticles, malignancy and thrombosis

被引:52
作者
Zahra, Sharon [1 ,2 ,3 ]
Anderson, Julia A. M. [1 ,2 ,3 ]
Stirling, David [1 ,2 ,3 ]
Ludlam, Christopher A. [1 ,2 ,3 ]
机构
[1] Univ Edinburgh, Coll Med & Vet Med, Edinburgh, Midlothian, Scotland
[2] Univ Edinburgh, Royal Infirm Edinburgh, Dept Clin, Edinburgh EH16 4SA, Midlothian, Scotland
[3] Univ Edinburgh, Royal Infirm Edinburgh, Haematol Lab, Edinburgh EH16 4SA, Midlothian, Scotland
关键词
microparticles; cancer; thrombosis; microparticle assays; immunophenotyping; PLATELET-DERIVED MICROPARTICLES; CIRCULATING ENDOTHELIAL MICROPARTICLES; FACTOR-BEARING MICROPARTICLES; FACTOR PROCOAGULANT ACTIVITY; TISSUE FACTOR EXPRESSION; FLOW-CYTOMETRIC ASSAY; P-SELECTIN; PLASMA MICROPARTICLES; CANCER PATIENTS; TUMOR-CELLS;
D O I
10.1111/j.1365-2141.2010.08452.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P>Microparticles (MPs) are considered to be important biological effectors of several different physiological and pathological processes. There is increasing evidence of their role in haemostasis and thrombosis, and also of their importance in cancer cell survival, invasiveness and metastasis. The level of circulating MPs has been assessed in many different disease states, and there are reports that patients with malignancy and patients with thrombosis have increased levels of circulating MPs and MP-dependent thrombogenic potential. Research into the function and effect of MPs is currently hampered by a lack of standardization in the methods used to identify and quantify them. As these methods improve it is likely that MP assays will be of use both diagnostically and therapeutically in the future.
引用
收藏
页码:688 / 700
页数:13
相关论文
共 85 条
[71]   Tissue factor activity is increased in a combined platelet and microparticle sample from cancer patients [J].
Tilley, Rachel E. ;
Holscher, Todd ;
Belani, Rajesh ;
Nieva, Jorge ;
Mackman, Nigel .
THROMBOSIS RESEARCH, 2008, 122 (05) :604-609
[72]  
Toth B, 2008, ANTICANCER RES, V28, P1107
[73]   Gender-specific and menstrual cycle dependent differences in circulating microparticlesy [J].
Toth, Bettina ;
Nikolajek, Katharina ;
Rank, Andreas ;
Nieuwland, Rienk ;
Lohse, Peter ;
Pihusch, Verena ;
Friese, Klaus ;
Thaler, Christian J. .
PLATELETS, 2007, 18 (07) :515-521
[74]   Isotype controls in phenotyping and quantification of microparticles: A major source of error and how to evade it [J].
Trummer, Arne ;
De Rop, Christiane ;
Tiede, Andreas ;
Ganser, Arnold ;
Eisert, Roswith .
THROMBOSIS RESEARCH, 2008, 122 (05) :691-700
[75]  
Ueno T, 2000, BRIT J CANCER, V83, P164
[76]  
van Doormaal FF, 2009, NETH J MED, V67, P266
[77]   Flow cytometry detection of platelet procoagulant activity and microparticles in patients with unstable angina treated by percutaneous coronary angioplasty and stent implantation [J].
Vidal, C ;
Spaulding, C ;
Picard, F ;
Schaison, F ;
Melle, J ;
Weber, S ;
Fontenay-Roupie, M .
THROMBOSIS AND HAEMOSTASIS, 2001, 86 (03) :784-790
[78]  
Vrana JA, 1996, CANCER RES, V56, P5063
[79]   Phosphatidylserine recognition by phagocytes: a view to a kill [J].
Wu, Y ;
Tibrewal, N ;
Birge, RB .
TRENDS IN CELL BIOLOGY, 2006, 16 (04) :189-197
[80]   Thrombin-induced platelet microparticles improved the aggregability of cryopreserved platelets [J].
Xiao, HY ;
Jepkorir, CJ ;
Harvey, K ;
Remick, DG .
CRYOBIOLOGY, 2002, 44 (02) :179-188