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Publication : IAP regulation of metastasis.

First Author  Mehrotra S Year  2010
Journal  Cancer Cell Volume  17
Issue  1 Pages  53-64
PubMed ID  20129247 Mgi Jnum  J:156930
Mgi Id  MGI:4422109 Doi  10.1016/j.ccr.2009.11.021
Citation  Mehrotra S, et al. (2010) IAP Regulation of Metastasis. Cancer Cell 17(1):53-64
abstractText  Inhibitor-of-Apoptosis (IAP) proteins contribute to tumor progression, but the requirements of this pathway are not understood. Here, we show that intermolecular cooperation between XIAP and survivin stimulates tumor cell invasion and promotes metastasis. This pathway is independent of IAP inhibition of cell death. Instead, a survivin-XIAP complex activates NF-kappaB, which in turn leads to increased fibronectin gene expression, signaling by beta1 integrins, and activation of cell motility kinases FAK and Src. Therefore, IAPs are direct metastasis genes, and their antagonists could provide antimetastatic therapies in patients with cancer.
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