Macrophage Binding to Receptor VCAM-1 Transmits Survival Signals in Breast Cancer Cells that Invade the Lungs

被引:514
作者
Chen, Qing [1 ]
Zhang, Xiang H. -F. [1 ]
Massague, Joan [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Howard Hughes Med Inst, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
MOLECULAR CHARACTERIZATION; ANGIOGENIC SWITCH; BONE METASTASIS; EXPRESSION; GROWTH; PROGRESSION; INVASION; ADHESION; PROTEIN; GENES;
D O I
10.1016/j.ccr.2011.08.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aberrant expression of vascular cell adhesion molecule-1 (VCAM-1) in breast cancer cells is associated with lung relapse, but the role of VCAM-1 as a mediator of metastasis has remained unknown. We report that VCAM-1 provides a survival advantage to breast cancer cells that infiltrate leukocyte-rich microenvironments such as the lungs. VCAM-1 tethers metastasis-associated macrophages to cancer cells via counter-receptor alpha 4-integrins. Clustering of cell surface VCAM-1, acting through Ezrin, triggers Akt activation and protects cancer cells from proapoptotic cytokines such as TRAIL. This prosurvival function of VCAM-1 can be blocked by antibodies against alpha 4-integrins. Thus, newly disseminated cancer cells expressing VCAM-1 can thrive in leukocyte-rich microenvironments through juxtacrine activation of a VCAM-1-Ezrin-PI3K/Akt survival pathway.
引用
收藏
页码:538 / 549
页数:12
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