Journal article
Binding of Anti-GRP78 Autoantibodies to Cell Surface GRP78 Increases Tissue Factor Procoagulant Activity via the Release of Calcium from Endoplasmic Reticulum Stores*
Abstract
The increased risk of venous thromboembolism in cancer patients has been attributed to enhanced tissue factor (TF) procoagulant activity (PCA) on the surface of cancer cells. Recent studies have shown that TF PCA can be modulated by GRP78, an endoplasmic reticulum (ER)-resident molecular chaperone. In this study, we investigated the role of cell surface GRP78 in modulating TF PCA in several human cancer cell lines. Although both GRP78 and TF …
Authors
Al-Hashimi AA; Caldwell J; Gonzalez-Gronow M; Pizzo SV; Aboumrad D; Pozza L; Al-Bayati H; Weitz JI; Stafford A; Chan H
Journal
Journal of Biological Chemistry, Vol. 285, No. 37, pp. 28912–28923
Publisher
Elsevier
Publication Date
September 2010
DOI
10.1074/jbc.m110.119107
ISSN
0021-9258
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Antibodies, NeoplasmAutoantibodiesCalciumCell Line, TumorEndoplasmic ReticulumEndoplasmic Reticulum Chaperone BiPEnzyme InhibitorsEpitopesHeat-Shock ProteinsHumansMalePhosphatidylserinesProstatic NeoplasmsSarcoplasmic Reticulum Calcium-Transporting ATPasesSignal TransductionThapsigarginThromboplastinType C PhospholipasesVenous Thromboembolism