Circulating endothelial cells, endothelial progenitor cells, and endothelial microparticles in cancer

被引:176
作者
Goon, P. K. Y.
Lip, G. Y. H.
Boos, C. J.
Stonelake, P. S.
Blann, A. D. [1 ]
机构
[1] City Hosp, Univ Dept Med, Haemostasis Thrombosis & Vasc Biol Unit, Birmingham B18 7QH, W Midlands, England
[2] Russells Hall Hosp, Dept Surg, Dudley DY1 2HQ, England
来源
NEOPLASIA | 2006年 / 8卷 / 02期
关键词
circulating endothelial cells; endothelial progenitor cells; endothelial microparticles; cancer; angiogenesis;
D O I
10.1593/neo.05592
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer, a proliferative disease hallmarked by abnormal cell growth and spread, is largely dependent on tumor neoangiogenesis, with evidence of vascular endothelial dysfunction. Novel ways to assess vascular function in cancer include measuring levels of circulating endothelial cells (CEC). Rare in healthy individuals, increased CEC in peripheral blood reflects significant vascular damage and dysfunction. They have been documented in many human diseases, including different types of cancers. An additional circulating cell population are endothelial progenitor cells (EPC), which have the ability to form endothelial colonies in vitro and may contribute toward vasculogenesis. At present, there is great interest in evaluating the role of EPC as novel markers for tumor angiogenesis and drug therapy monitoring. Recently, exocytic procoagulant endothelial microparticles (EMP) have also been identified. CEC, EPC, and EMP research works may have important clinical implications but are often impeded by methodological issues and a lack of consensus on phenotypic identification of these cells and particles. This review aims to collate existing literature and provide an overview on the current position of CEC, EPC, and EMP in cell biology terms and to identify their significance to clinical medicine, with particular emphasis on relationship with cancer.
引用
收藏
页码:79 / 88
页数:10
相关论文
共 94 条
[1]  
Adams J, 2000, CANCER RES, V60, P2898
[2]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[3]   Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228
[4]   VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[5]   Circulating endothelial cells in cancer patients do not express tissue factor [J].
Beerepoot, LV ;
Mehra, N ;
Linschoten, F ;
Jorna, AS ;
Lisman, T ;
Verheul, HMW ;
Voest, EE .
CANCER LETTERS, 2004, 213 (02) :241-248
[6]   Increased levels of viable circulating endothelial cells are an indicator of progressive disease in cancer patients [J].
Beerepoot, LV ;
Mehra, N ;
Vermaat, JSP ;
Zonnenberg, BA ;
Gebbink, MFGB ;
Voest, EE .
ANNALS OF ONCOLOGY, 2004, 15 (01) :139-145
[7]  
Bertolini F, 2003, CANCER RES, V63, P4342
[8]   Assessment of endothelial dysfunction: Focus on atherothrombotic disease [J].
Blann, AD .
PATHOPHYSIOLOGY OF HAEMOSTASIS AND THROMBOSIS, 2003, 33 (5-6) :256-261
[9]  
BLANN AD, 2005, THROMB HAEMOSTASIS, V93, P1
[10]   Circulating microparticles from patients with myocardial infarction cause endothelial dysfunction [J].
Boulanger, CM ;
Scoazec, A ;
Ebrahimian, T ;
Henry, P ;
Mathieu, E ;
Tedgui, A ;
Mallat, Z .
CIRCULATION, 2001, 104 (22) :2649-2652