4.7 Review

Digesting a Path Forward: The Utility of Collagenase Tumor Treatment for Improved Drug Delivery

Journal

MOLECULAR PHARMACEUTICS
Volume 15, Issue 6, Pages 2069-2083

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.8b00319

Keywords

extracellular matrix; collagenase; hyaluronidase; interstitial fluid pressure; drug penetration; drug diffusion

Funding

  1. NIH [T32 GM007175]
  2. National Science Foundation

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Collagen and hyaluronan are the most abundant components of the extracellular matrix (ECM) and their overexpression in tumors is linked to increased tumor growth and metastasis. These ECM components contribute to a protective tumor microenvironment by supporting a high interstitial fluid pressure and creating a tortuous setting for the convection and diffusion of chemotherapeutic small molecules, antibodies, and nanoparticles in the tumor interstitial space. This review focuses on the research efforts to deplete extracellular collagen with collagenases to normalize the tumor microenvironment. Although collagen synthesis inhibitors are in clinical development, the use of collagenases is contentious and clinically untested in cancer patients. Pretreatment of murine tumors with collagenases increased drug uptake and diffusion 2-10-fold. This modest improvement resulted in decreased tumor growth, but the benefits of collagenase treatment are confounded by risks of toxicity from collagen breakdown in healthy tissues. In this review, we evaluate the published in vitro and in vivo benefits and limitations of collagenase treatment to improve drug delivery.

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