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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

The EphB4 receptor suppresses breast cancer cell tumorigenicity through an Abl-Crk pathway.

Recent evidence supports a role for EphB receptor tyrosine kinases as tumour suppressors in colorectal and prostate cancer. However, it is unclear how these receptors inhibit cancer cell tumorigenicity - an activity that is highly unusual for a family of receptor tyrosine kinases. Here, we report that the EphB4 receptor can behave as a tumour suppressor in a mouse xenograft model of breast cancer when stimulated by its ligand, ephrin-B2. In breast cancer cells, EphB4 activates an antioncogenic pathway involving Abl family tyrosine kinases and the Crk adaptor protein. This Abl-Crk pathway inhibits breast cancer cell viability and proliferation in addition to motility and invasion, and also downregulates the pro-invasive matrix metalloprotease, MMP-2. Consistent with these effects, EphB4 and the Abl-Crk pathway are constitutively active in non-transformed mammary epithelial cells. These findings identify a novel Eph receptor signalling pathway with tumour-suppressor activity and predict that therapeutic intervention to activate EphB4 signalling will inhibit tumour progression.[1]


  1. The EphB4 receptor suppresses breast cancer cell tumorigenicity through an Abl-Crk pathway. Noren, N.K., Foos, G., Hauser, C.A., Pasquale, E.B. Nat. Cell Biol. (2006) [Pubmed]
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