Disrupting the Scaffold to Improve Focal Adhesion Kinase–Targeted Cancer Therapeutics

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Science Signaling  19 Mar 2013:
DOI: 10.1126/scisignal.2004021


Focal adhesion kinase (FAK) is emerging as a promising cancer target because it is highly expressed at both the transcriptional and translational level in cancer and is involved in many aspects of tumor growth, invasion, and metastasis. Existing FAK-based therapeutics focus on inhibiting the kinase’s catalytic function and not the large scaffold it creates that includes many oncogenic receptor tyrosine kinases and tumor suppressor proteins. Targeting the FAK scaffold is a feasible and promising approach for developing highly specific therapeutics that disrupt FAK signaling pathways in cancer.

Full article available 26 March 2013, Vol. 6, Issue 268, pe10

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