Cancer cell binding to E-selectin transfected human endothelia.

Abstract:

:Human endothelial cells were transiently transfected with E-Selectin which enabled us to study tumor cell/endothelial interactions following engagement of E-Selectin without the added complications of metabolic stimulation, morphological changes, and/or up regulation of other adhesion molecules due to cytokine induction. Similar results were received from in vitro binding studies and FACS analyses on both Tumor Necrosis Factor-alpha activated and E-Selectin transfected endothelial cells. These data suggest that this methodology is appropriate for dissecting the individual activities of E-selectin while minimizing the participation of other adhesion molecules, thereby allowing us to develop a better understanding of the role of E-Selectin and endothelia in metastatic disease.

authors

Merwin JR,Madri JA,Lynch M

doi

10.1016/0006-291x(92)91560-d

subject

Has Abstract

pub_date

1992-11-30 00:00:00

pages

315-23

issue

1

eissn

0006-291X

issn

1090-2104

pii

0006-291X(92)91560-D

journal_volume

189

pub_type

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