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

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Science Signaling  26 Mar 2013:
Vol. 6, Issue 268, pp. pe10
DOI: 10.1126/scisignal.2004021

Article Information

vol. 6 no. 268 pe10

DOI: 
https://doi.org/10.1126/scisignal.2004021
PubMed: 
23532331
Published By: 
Science Signaling
Print ISSN: 
1945-0877
Online ISSN: 
1937-9145
History: 
  • .

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Copyright & Usage: 
Copyright © 2013, American Association for the Advancement of Science

Author Information

  1. William G. Cance1,2,3,*,
  2. Elena Kurenova1,3,
  3. Timothy Marlowe1, and
  4. Vita Golubovskaya1,3
  1. 1Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA.
  2. 2Department of Surgery, University at Buffalo, State University of New York, Elm and Carlton Streets, Buffalo, NY 14263, USA.
  3. 3CureFAKtor Pharmaceuticals, LLC, 14 Rockdove Lane, Orchard Park, NY 14127, USA.
  1. ↵*Corresponding author. E-mail: william.cance{at}roswellpark.org

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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 Signaling : pe10

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

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