Abstract
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 α4-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 α4-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.
| Original language | English |
|---|---|
| Pages (from-to) | 538-549 |
| Number of pages | 12 |
| Journal | Cancer Cell |
| Volume | 20 |
| Issue number | 4 |
| DOIs | |
| State | Published - Oct 18 2011 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Animals
- Breast Neoplasms/genetics
- Cell Adhesion/immunology
- Cytoskeletal Proteins/metabolism
- Female
- Humans
- Leukocytes/immunology
- Lung Neoplasms/secondary
- Macrophages/metabolism
- Mice
- Neoplastic Cells, Circulating/immunology
- Oncogene Protein v-akt/metabolism
- Signal Transduction
- Vascular Cell Adhesion Molecule-1/genetics
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