Interactions between osteopontin and vascular endothelial growth factor: Implications for cancer

被引:37
|
作者
Ramchandani, Divya [1 ]
Weber, Georg F. [1 ]
机构
[1] Univ Cincinnati, James L Winkle Coll Pharm, Cincinnati, OH 45267 USA
来源
关键词
Angiogenesis; Hypoxia; Apoptosis; Cancer; Vascular disease; Immune system; MARROW STROMAL CELLS; BONE MORPHOGENETIC PROTEINS; EPITHELIAL OVARIAN-CANCER; BIOACTIVE GLASS SCAFFOLDS; GENE-EXPRESSION ANALYSIS; BREAST-TUMOR GROWTH; IN-VITRO; OSTEOGENIC DIFFERENTIATION; EXTRACELLULAR-MATRIX; PROSTATE-CANCER;
D O I
10.1016/j.bbcan.2015.02.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For this comprehensive review, 257 publications with the keywords "osteopontin" or "OPN" and "vascular endothelial growth factor" or "VEGF" in PubMed were screened (time frame from year 1996 to year 2014). 37 articles were excluded because they were not focused on the interactions between these molecules, and papers relevant for transformation-related phenomena were selected. Osteopontin (OPN) and vascular endothelial growth factor (VEGF) are characterized by a convergence in function for regulating cell motility and angiogenesis, the response to hypoxia, and apoptosis. Often, they are co-expressed or one molecule induces the other, however, in some settings OPN-associated pathways and VEGF-associated pathways are distinct. Their relationships affect the pathogenesis in cancer, where they contribute to progression and angiogenesis and serve as markers for poor prognosis. The inhibition of OPN may reduce VEGF levels and suppress tumor progression. In vascular pathologies, these two cytokines mediate remodeling, but may also perpetuate inflammation and narrowing of the arteries. OPN and VEGF are elevated and contribute to vascularization in inflammatory diseases. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:202 / 222
页数:21
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