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

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vol. 6 no. 268 pe10

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https://doi.org/10.1126/scisignal.2004021

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Copyright © 2013, American Association for the Advancement of Science

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William G. Cance¹,²,³,*,
Elena Kurenova¹,³,
Timothy Marlowe¹, and
Vita Golubovskaya¹,³

¹Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA.
²Department of Surgery, University at Buffalo, State University of New York, Elm and Carlton Streets, Buffalo, NY 14263, USA.
³CureFAKtor Pharmaceuticals, LLC, 14 Rockdove Lane, Orchard Park, NY 14127, USA.

↵*Corresponding author. E-mail: william.cance{at}roswellpark.org

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Science Signaling: 6 (268)

Science Signaling

Vol 6, Issue 268
26 March 2013

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

By William G. Cance, Elena Kurenova, Timothy Marlowe, Vita Golubovskaya

Science Signaling26 Mar 2013 : pe10

Targeting the scaffold of focal adhesion kinase is a therapeutic opportunity to inhibit signaling pathways selectively in cancer cells.

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

By William G. Cance, Elena Kurenova, Timothy Marlowe, Vita Golubovskaya

Science Signaling26 Mar 2013 : pe10

Targeting the scaffold of focal adhesion kinase is a therapeutic opportunity to inhibit signaling pathways selectively in cancer cells.

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