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Generation of a multi-functional, target organ-specific, anti-fibrotic molecule by molecular engineering of the extracellular matrix protein, decorin

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 176, Issue 1, Pages 16-25

Publisher

WILEY
DOI: 10.1111/bph.14374

Keywords

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Funding

  1. Academy of Finland
  2. Paivikki and Sakari Sohlberg Foundation
  3. Pirkanmaa Hospital District Research Foundation
  4. Diabetes Wellness Foundation
  5. Tampere Tuberculosis Foundation

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Extracellular matrix (ECM) molecules play important roles in regulating processes such as cell proliferation, migration, differentiation and survival. Decorin is a proteoglycan that binds to ('decorates') collagen fibrils in the ECM. Decorin also interacts with many growth factors and their receptors, the most notable of these interactions being its inhibitory activity on TGF-beta, the growth factor responsible for fibrosis formation. We have generated a recombinant, multi-functional, fusion-protein consisting of decorin as a therapeutic domain and a vascular homing and cell-penetrating peptide as a targeting vehicle. This recombinant decorin (CAR-DCN) accumulates at the sites of the targeted disease at higher levels and, as a result, has substantially enhanced biological activity over native decorin. CAR-DCN is an example of how molecular engineering can give a compound the ability to seek out sites of disease and enhance its therapeutic potential. CAR-DCN will hopefully be used to treat severe human diseases.

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