P-selectin cell adhesion molecule in inflammation, thrombosis, cancer growth and metastasis

被引:86
作者
Geng, JG [1 ]
Chen, M
Chou, KC
机构
[1] Univ Minnesota, Sch Med, Vasc Biol Ctr, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Div Hematol Oncol & Transplantat, Minneapolis, MN 55455 USA
[3] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Mol Cell Biol Lab, Shanghai 200031, Peoples R China
[4] Tianjin Inst Bioinformat & Drug Discovery, Tianjin 300074, Peoples R China
[5] Shanghai Jiao Tong Univ, Life Sci Res Ctr, Shanghai 200030, Peoples R China
[6] Gordon Life Sci Inst, San Diego, CA 92130 USA
关键词
selectin; cell adhesion molecule; leukocyte; platelet; endothelial cell; cancer cell; inflammation; thrombosis; cancer growth and metastasis;
D O I
10.2174/0929867043364720
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
P-selectin (CD62P) is a member of the selectin family of cell adhesion molecules. It is expressed on stimulated endothelial cells and activated platelets and mediates leukocyte rolling on stimulated endothelial cells and heterotypic aggregation of activated platelets onto leukocytes. It also mediates heterotypic aggregation of activated platelets to cancer cells and adhesion of cancer cells to stimulated endothelial cells. Using P-selectin knockout mice, the importance of P-selectin-mediated cell adhesive interactions in the pathogeneses of inflammation, thrombosis, growth and metastasis of cancers has been clearly demonstrated. Here we will summarize the current knowledge and highlight the important progress in the biomedical research of P-selectin biology, providing a suitable target for therapeutic interventions developed through both experimental and bioinformatic approaches.
引用
收藏
页码:2153 / 2160
页数:8
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