Mechanisms of PECAM-1-mediated cytoprotection and implications for cancer cell survival

被引:31
作者
Bergom, C
Gao, CJ
Newman, P
机构
[1] Blood Ctr SE Wisconsin Inc, Blood Res Inst, Milwaukee, WI 53233 USA
[2] Med Coll Wisconsin, Dept Anat Cell Biol & Neurobiol, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Ctr Cardiovasc, Milwaukee, WI 53226 USA
关键词
PECAM-1; SHP-2; apoptosis; cancer; leukemia;
D O I
10.1080/10428190500126091
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Defects in apoptotic pathways can promote cancer development and cause cancers to become resistant to chemotherapy. The cell adhesion and signaling molecule PECAM-1 has been shown to potently suppress apoptosis in a variety of cellular systems. PECAM-1 expression has been reported on a variety of human malignancies-especially hematopoietic and vascular cell cancers-but the significance of this expression has not been fully explored. The ability of PECAM-1 to inhibit apoptosis makes it an attractive candidate as a molecule that may promote cancer development and/or confer resistance to chemotherapeutic treatment. The exact mechanisms by which PECAM-1 mediates its cytoprotection have not been fully defined, but its anti-apoptotic effects have been shown to require both homophilic binding and intracellular signaling via its immunoreceptor tyrosine-based inhibitory motif (ITIM) domains. In this review, we will discuss the data regarding PECAM-1's anti-apoptotic effects and ways in which this cytoprotection may be clinically relevant to the development and/or treatment of hematologic malignancies that express this vascular cell-specific surface molecule.
引用
收藏
页码:1409 / 1421
页数:13
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