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New approaches to targeting the actin cytoskeleton for chemotherapy

Journal

FUTURE MEDICINAL CHEMISTRY
Volume 1, Issue 7, Pages 1311-1331

Publisher

FUTURE SCI LTD
DOI: 10.4155/FMC.09.99

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Funding

  1. National Health and Medical Research Council (NHMRC) of Australia
  2. Oncology Children's Foundation

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The actin cytoskeleton is indispensable for normal cellular function. In particular, several actin-based structures coordinate cellular motility, a process hijacked by tumor cells in order to facilitate their propagation to distant sites. The actin cytoskeleton, therefore, represents a point for chemotherapeutic intervention. The challenge in disrupting the actin cytoskeleton is in preserving actin-driven contraction of cardiac and skeletal muscle. By targeting actin-binding proteins with altered expression in malignancy, it may be possible to achieve tumor-specific toxicity. A number of actin-binding proteins act cooperatively and synergistically to regulate actin structures required for motility. The actin cytoskeleton is characterized by a significant degree of plasticity. Targeting specific actin-binding proteins for chemotherapy will only be successful if no other compensatory mechanisms exist.

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