| Literature DB >> 29767984 |
Aaron Dolor1, Francis C Szoka1.
Abstract
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.Entities:
Keywords: collagenase; drug diffusion; drug penetration; extracellular matrix; hyaluronidase; interstitial fluid pressure
Mesh:
Substances:
Year: 2018 PMID: 29767984 PMCID: PMC6764447 DOI: 10.1021/acs.molpharmaceut.8b00319
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939