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Research ArticleOriginal Article
Open Access

Monocyte tissue factor levels in cancer patients

Bashir A. Lwaleed, John L. Francis and Morag Chisholm
Saudi Medical Journal August 2000, 21 (8) 722-729;
Bashir A. Lwaleed
University Department of Haematology Level F (827), South Academic Block, Southampton General Hospital, Tremona Road, Southampton, SO16 6YD, United Kingdom. Tel/Fax. +44 (2380) 796580. E-mail. [email protected]
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  • For correspondence: [email protected]
John L. Francis
Thrombosis Research Unit, Walt Disney Memorial Cancer Institute at Florida Hospital, Florida, United States of America.
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Morag Chisholm
University Department of Hematology, Southampton University Hospitals, Southampton, United Kingdom.
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Abstract

OBJECTIVE: The association between cancer and thromboembolic disease has been known for over a century. Increased tissue factor expression by endothelial cells, monocytes or macrophages is implicated. Thus, monocyte tissue factor measurements may reflect disease presence or progression.

METHODS: Using a 2 stage kinetic chromogenic assay, monocyte tissue factor levels were assessed in normal controls (n=60), patient controls (hernia or cholecystectomy, n=60) and in patients with benign and malignant disease of the bladder (n=73), prostate (n=81), breast (n=83) and colorectum (n=62). This was performed as baseline (resting cells) and after 6 hours incubation with (stimulated) and without (unstimulated) lipopolysaccharide. Each benign disease group was sub-divided into inflammatory and non-inflammatory categories.

RESULTS: The relative operating characteristic curve for the lipopolysaccharide-stimulated monocyte tissue factor assay showed sensitivity and specificity for cancer, the area under the curve being 0.71. The control groups and the benign non-inflammatory groups gave similar results and were pooled for further analysis. Each malignant group showed higher monocyte tissue factor levels than the control groups for baseline (P< 0.05) and lipopolysaccharide-stimulated cells (P< 0.05). All benign inflammatory groups apart from breast, showed increased monocyte tissue factor levels over controls for baseline (P< 0.05) and lipopolysaccharide-stimulated cells (P< 0.05). In all cases there was no significant difference between the malignant and the benign inflammatory groups. Monocyte tissue factor levels were related to tumor grade or stage, patients’ survival time, serum prostate specific antigen and static bone scan images. Levels were also higher in patients with bladder cancer recurrence and in those who subsequently died.

CONCLUSION: Lipopolysaccharide-stimulated monocyte tissue factor assay showed sensitivity and specificity for cancer compared to controls. Monocyte tissue factor levels are raised in malignant groups compared to controls and non-inflammatory diseases but not when compared with inflammatory conditions. Stimulated cells give better discrimination between the groups and may be useful in identifying high risk individuals. Monocyte tissue factor levels were related to tumor progression.

  • Copyright: © Saudi Medical Journal

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Saudi Medical Journal: 21 (8)
Saudi Medical Journal
Vol. 21, Issue 8
1 Aug 2000
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Monocyte tissue factor levels in cancer patients
Bashir A. Lwaleed, John L. Francis, Morag Chisholm
Saudi Medical Journal Aug 2000, 21 (8) 722-729;

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Monocyte tissue factor levels in cancer patients
Bashir A. Lwaleed, John L. Francis, Morag Chisholm
Saudi Medical Journal Aug 2000, 21 (8) 722-729;
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© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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