Silencing of secreted protein acidic and rich in cysteine inhibits the growth of human melanoma cells with G1 arrest induction
Author:
Publisher
Wiley
Subject
Cancer Research,Oncology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1349-7006.2009.01476.x/fullpdf
Reference34 articles.
1. SPARC, a matricellular protein that functions in cellular differentiation and tissue response to injury;Bradshaw;J Clin Invest,2001
2. SPARC, a matricellular glycoprotein with important biological functions;Yan;J Histochem Cytochem,1999
3. SPARC antagonizes the effect of basic fibroblast growth factor on the migration of bovine aortic endothelial cells;Hasselaar;J Cell Biochem,1992
4. The extracellular glycoprotein SPARC interacts with platelet-derived growth factor (PDGF)-AB and -BB and inhibits the binding of PDGF to its receptors;Raines;Proc Natl Acad Sci U S A,1992
5. SPARC (BM-40, osteonectin) inhibits the mitogenic effect of vascular endothelial growth factor on microvascular endothelial cells;Kupprion;J Biol Chem,1998
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1. SPARC: a potential target for functional nanomaterials and drugs;Frontiers in Molecular Biosciences;2023-07-28
2. SPARC is down-regulated by DNA methylation and functions as a tumor suppressor in T-cell lymphoma;Experimental Cell Research;2018-03
3. Prognostic significance of immunohistochemical epithelial–mesenchymal transition markers in skin melanoma patients;Biomarkers in Medicine;2016-09
4. The secreted protein acidic and rich in cysteine is a critical mediator of cell death program induced by WIN/TRAIL combined treatment in osteosarcoma cells;International Journal of Oncology;2015-12-24
5. Expression of secreted protein acidic and rich in cysteine is an independent prognostic indicator of a poor clinical outcome in oropharyngeal carcinoma patients;Acta Oto-Laryngologica;2015-11-02
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