Increased activity of cell membrane-associated prothrombinase, fibrinogen-like protein 2, in peripheral blood mononuclear cells of B-cell lymphoma patients

Fibrinogen-like protein 2, FGL-2, was reported to be overexpressed in various cancer tissues, where it acts as a transmembrane prothrombinase. This study aims to determine the prothrombinase activity of FGL-2 in peripheral blood mononuclear cells (PBMC) of patients with B-cell lymphoma. FGL-2 activi...

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Published inPloS one Vol. 9; no. 10; p. e109648
Main Authors Rabizadeh, Esther, Cherny, Izhack, Wolach, Ofir, Sherman, Shany, Binkovski, Natalia, Peretz, Alon, Lederfein, Doron, Inbal, Aida
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 10.10.2014
Public Library of Science (PLoS)
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Summary:Fibrinogen-like protein 2, FGL-2, was reported to be overexpressed in various cancer tissues, where it acts as a transmembrane prothrombinase. This study aims to determine the prothrombinase activity of FGL-2 in peripheral blood mononuclear cells (PBMC) of patients with B-cell lymphoma. FGL-2 activity was determined in patients with B-cell lymphoma (n = 53), and healthy controls (n = 145). FGL-2 activity in patients at diagnosis increased 3 ± 0.3 fold (p < 0.001). Sensitivity and specificity of the test was established at 73.6% and 80.7%, respectively, using a cutoff of 150% activity over control. Moreover, FGL-2 activity in 10 of 11 patients in remission decreased by 76%. In contrast, no significant difference was observed in expression levels of fgl-2 gene in patients and controls. Taken together, our study indicates that FGL-2 prothrombinase activity in PBMC of lymphoma patients is increased in active disease and normalizes during remission, thus being a potential marker for follow up of lymphoma patients.
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: ER IC DL AI. Performed the experiments: IC DL NB. Analyzed the data: IC DL OW SS. Contributed reagents/materials/analysis tools: ER OW SS AP AI. Wrote the paper: ER IC OW SS NB AP DL AI.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0109648