Role of calcium in E-selectin induced phenotype of T84 colon carcinoma cells

被引:14
作者
D'Amato, M
Flugy, AM
Alaimo, G
Bauder, B
Kohn, EC
De Leo, G
Alessandro, R
机构
[1] Univ Palermo, Dipartimento Biopatol & Metodol Biomed, I-90133 Palermo, Italy
[2] NCI, Pathol Lab, Mol Signaling Sect, Bethesda, MD 20892 USA
关键词
E-selectin; calcium signaling; metastasis; colon carcinoma; tumor cells;
D O I
10.1016/S0006-291X(03)00062-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The adhesion of cancer cells to the endothelium during the metastatic process involves the interaction of specific cell-cell adhesion receptors on the cell surface. E-selectin on endothelial cells and sialyl Lewis X carbohydrate component on tumor cells are mainly implicated in the adhesion of colon carcinoma cells to the endothelium of target organ. In this paper we show that binding of E-selectin to T84 colon tumor cells causes approximately a twofold increase in intracellular calcium concentration. In particular, using two inhibitors of receptor operated calcium channels, CAI and SK&F 96365, we present evidences that the augmentation in cytoplasmic calcium originates from ionic influx from extracellular sources. Furthermore, we demonstrated that modulation of [Ca2+](i) by engagement of E-selectin receptor starts signal transduction pathways that affect cell spreading, tyrosine phosphorylation signaling, and cancer cell motility. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:907 / 914
页数:8
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