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Anticoagulation Inhibits Tumor Cell-mediated Release of Platelet Angiogenic Proteins and Diminishes Platelet Angiogenic Response

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 2013 Sep 26
PMID 24065244
Citations 48
Authors
Affiliations
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Abstract

Platelets are a reservoir for angiogenic proteins that are secreted in a differentially regulated process. Because of the propensity for clotting, patients with malignancy are often anticoagulated with heparin products, which paradoxically offer a survival benefit by an unknown mechanism. We hypothesized that antithrombotic agents alter the release of angiogenesis regulatory proteins from platelets. Our data revealed that platelets exposed to heparins released significantly decreased vascular endothelial growth factor (VEGF) in response to adenosine 5'-diphosphate or tumor cells (MCF-7 cells) and exhibited a decreased angiogenic potential. The releasate from these platelets contained decreased proangiogenic proteins. The novel anticoagulant fondaparinux (Xa inhibitor) demonstrated a similar impact on the platelet angiogenic potential. Because these anticoagulants decrease thrombin generation, we hypothesized that they disrupt signaling through the platelet protease-activated receptor 1 (PAR1) receptor. Addition of PAR1 antagonists to platelets decreased VEGF release and angiogenic potential. Exposure to a PAR1 agonist in the presence of anticoagulants rescued the angiogenic potential. In vivo studies demonstrated that platelets from anticoagulated patients had decreased VEGF release and angiogenic potential. Our data suggest that the mechanism by which antithrombotic agents increase survival and decrease metastasis in cancer patients is through attenuation of platelet angiogenic potential.

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References
1.
Bambace N, Levis J, Holmes C . The effect of P2Y-mediated platelet activation on the release of VEGF and endostatin from platelets. Platelets. 2010; 21(2):85-93. DOI: 10.3109/09537100903470298. View

2.
Lee A, Rogers L, Longcroft J, Jeffery R . Reduction of metastasis in a murine mammary tumour model by heparin and polyinosinic-polycytidylic acid. Clin Exp Metastasis. 1990; 8(2):165-71. DOI: 10.1007/BF00117789. View

3.
Marchetti M, Diani E, Ten Cate H, Falanga A . Characterization of the thrombin generation potential of leukemic and solid tumor cells by calibrated automated thrombography. Haematologica. 2012; 97(8):1173-80. PMC: 3409814. DOI: 10.3324/haematol.2011.055343. View

4.
Gay L, Felding-Habermann B . Contribution of platelets to tumour metastasis. Nat Rev Cancer. 2011; 11(2):123-34. PMC: 6894505. DOI: 10.1038/nrc3004. View

5.
Boukerche H, Berthier-Vergnes O, Penin F, Tabone E, Lizard G, Bailly M . Human melanoma cell lines differ in their capacity to release ADP and aggregate platelets. Br J Haematol. 1994; 87(4):763-72. DOI: 10.1111/j.1365-2141.1994.tb06736.x. View