Literature DB >> 19861441

Tumor-derived tissue factor-bearing microparticles are associated with venous thromboembolic events in malignancy.

Jeffrey I Zwicker1, Howard A Liebman, Donna Neuberg, Romaric Lacroix, Kenneth A Bauer, Barbara C Furie, Bruce Furie.   

Abstract

PURPOSE: Despite the strong association between malignant disease and thromboembolic disorders, the molecular and cellular basis of this relationship remains uncertain. We evaluated the hypothesis that tumor-derived tissue factor-bearing microparticles in plasma contribute to cancer-associated thrombosis. EXPERIMENTAL
DESIGN: We developed impedance-based flow cytometry to detect, quantitate, and size microparticles in platelet-poor plasma. We evaluated the number of tissue factor-bearing microparticles in a cohort of cancer patients of different histologies (N = 96) and conducted a case-control study of 30 cancer patients diagnosed with an acute venous thromboembolic event (VTE) compared with 60 cancer patients of similar age, stage, sex, and diagnosis without known VTE, as well as 22 patients with an idiopathic VTE.
RESULTS: Tissue factor-bearing microparticles were detected in patients with advanced malignancy, including two thirds of patients with pancreatic carcinoma. Elevated levels of tissue factor-bearing microparticles were associated VTE in cancer patients (adjusted odds ratio, 3.72; 95% confidence interval, 1.18-11.76; P = 0.01). In cancer patients without VTE, a retrospective analysis revealed a 1-year cumulative incidence of VTE of 34.8% in patients with tissue factor-bearing microparticles versus 0% in those without detectable tissue factor-bearing microparticles (Gray test P = 0.002).The median number of tissue factor-bearing microparticles in the cancer VTE cohort (7.1 x 10(4) microparticles/microL) was significantly greater than both the idiopathic VTE and cancer-no VTE groups (P = 0.002 and P = 0.03, respectively). Pancreatectomy in three patients eliminated or nearly eliminated these microparticles which coexpressed the epithelial tumor antigen, MUC-1.
CONCLUSION: We conclude that tumor-derived tissue factor-bearing microparticles are associated with VTE in cancer patients and may be central to the pathogenesis of cancer-associated thrombosis.

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Year:  2009        PMID: 19861441      PMCID: PMC2783253          DOI: 10.1158/1078-0432.CCR-09-0371

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  43 in total

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2.  Tumor shedding and coagulation.

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3.  Activation of blood coagulation in cancer: Trousseau's syndrome revisited.

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4.  Disseminated intravascular coagulation in solid tumors: clinical and pathologic study.

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Review 5.  Tissue factor, thrombin, and cancer.

Authors:  Frederick R Rickles; Steven Patierno; Patricia M Fernandez
Journal:  Chest       Date:  2003-09       Impact factor: 9.410

Review 6.  MUC1 and MUC2 in pancreatic neoplasia.

Authors:  E Levi; D S Klimstra; A Andea; O Basturk; N V Adsay
Journal:  J Clin Pathol       Date:  2004-05       Impact factor: 3.411

7.  Plasma tissue factor may be predictive of venous thromboembolism in pancreatic cancer.

Authors:  A A Khorana; C W Francis; K E Menzies; J-G Wang; O Hyrien; J Hathcock; N Mackman; M B Taubman
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Authors:  S G Gordon; B A Cross
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Authors:  Arun S Shet; Omer Aras; Kalpna Gupta; Mathew J Hass; Douglas J Rausch; Nabil Saba; Louann Koopmeiners; Nigel S Key; Robert P Hebbel
Journal:  Blood       Date:  2003-06-12       Impact factor: 22.113

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  144 in total

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Review 5.  Primary venous thromboembolism prophylaxis in patients with solid tumors: a meta-analysis.

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Review 7.  Thrombosis in cancer patients: etiology, incidence, and management.

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Review 8.  Emerging paradigms in arterial thrombosis.

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9.  Physiological levels of blood coagulation factors IX and X control coagulation kinetics in an in vitro model of circulating tissue factor.

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10.  Prediction and prevention of thromboembolic events with enoxaparin in cancer patients with elevated tissue factor-bearing microparticles: a randomized-controlled phase II trial (the Microtec study).

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