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Decorin as a multivalent therapeutic agent against cancer
- Source :
- Advanced Drug Delivery Reviews. 97:174-185
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Decorin is a prototypical small leucine-rich proteoglycan and epitomizes the multifunctional nature of this critical gene family. Soluble decorin engages multiple receptor tyrosine kinases within the target rich environment of the tumor stroma and tumor parenchyma. Upon receptor binding, decorin initiates signaling pathways within endothelial cells downstream of VEGFR2 that ultimately culminate in a Peg3/Beclin 1/LC3-dependent autophagic program. Concomitant with autophagic induction, decorin blunts capillary morphogenesis and endothelial cell migration, thereby significantly compromising tumor angiogenesis. In parallel within the tumor proper, decorin binds multiple RTKs with high affinity, including Met, for a multitude of oncosuppressive functions including growth inhibition, tumor cell mitophagy, and angiostasis. Decorin is also pro-inflammatory by modulating macrophage function and cytokine secretion. Decorin suppresses tumorigenic growth, angiogenesis, and prevents metastatic lesions in a variety of in vitro and in vivo tumor models. Therefore, decorin would be an ideal therapeutic candidate for combatting solid malignancies.
- Subjects :
- 0301 basic medicine
Decorin
Angiogenesis
Pharmaceutical Science
Article
Receptor tyrosine kinase
03 medical and health sciences
0302 clinical medicine
Neoplasms
Autophagy
Animals
Humans
ROCK1
Neovascularization, Pathologic
biology
Genetic Therapy
Proto-Oncogene Proteins c-met
ErbB Receptors
carbohydrates (lipids)
Vascular endothelial growth factor A
030104 developmental biology
Proteoglycan
030220 oncology & carcinogenesis
biology.protein
Cancer research
Cytokine secretion
Platelet-derived growth factor receptor
Subjects
Details
- ISSN :
- 0169409X
- Volume :
- 97
- Database :
- OpenAIRE
- Journal :
- Advanced Drug Delivery Reviews
- Accession number :
- edsair.doi.dedup.....dc5a39ac9af46dbc6834774b744c5f4a
- Full Text :
- https://doi.org/10.1016/j.addr.2015.10.016