Role of the metastasis-promoting protein osteopontin in the tumour microenvironment

被引:181
作者
Anborgh, Pieter H. [1 ]
Mutrie, Jennifer C. [1 ,2 ]
Tuck, Alan B. [1 ,2 ,3 ,4 ]
Chambers, Ann F. [1 ,2 ,4 ]
机构
[1] London Reg Canc Program, London, ON N6A 4L6, Canada
[2] Univ Western Ontario, Dept Pathol, London, ON, Canada
[3] London Hlth Sci Ctr, Dept Pathol, London, ON, Canada
[4] Univ Western Ontario, Dept Oncol, London, ON, Canada
基金
加拿大健康研究院;
关键词
osteopontin; tumour microenvironment; bone microenvironment; metastasis; angiogenesis; ENDOTHELIAL GROWTH-FACTOR; MAMMARY EPITHELIAL-CELLS; BREAST-CANCER MALIGNANCY; HEPATOCELLULAR-CARCINOMA; PROSTATE-CANCER; SECRETED PHOSPHOPROTEIN; MACROPHAGES PROMOTE; ADHESIVE PROPERTIES; PLASMA OSTEOPONTIN; BONE SIALOPROTEIN;
D O I
10.1111/j.1582-4934.2010.01115.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Osteopontin (OPN) is a secreted protein present in bodily fluids and tissues. It is subject to multiple post-translational modifications, including phosphorylation, glycosylation, proteolytic cleavage and crosslinking by transglutamination. Binding of OPN to integrin and CD44 receptors regulates signalling cascades that affect processes such as adhesion, migration, invasion, chemotaxis and cell survival. A variety of cells and tissues express OPN, including bone, vasculature, kidney, inflammatory cells and numerous secretory epithelia. Normal physiological roles include regulation of immune functions, vascular remodelling, wound repair and developmental processes. OPN also is expressed in many cancers, and elevated levels in patients' tumour tissue and blood are associated with poor prognosis. Tumour growth is regulated by interactions between tumour cells and their tissue microenvironment. Within a tumour mass, OPN can be expressed by both tumour cells and cellular components of the tumour microenvironment, and both tumour and normal cells may have receptors able to bind to OPN. OPN can also be found as a component of the extracellular matrix. The functional roles of OPN in a tumour are thus complex, with OPN secreted by both tumour cells and cells in the tumour microenvironment, both of which can in turn respond to OPN. Much remains to be learned about the cross-talk between normal and tumour cells within a tumour, and the role of multiple forms of OPN in these interactions. Understanding OPN-mediated interactions within a tumour will be important for the development of therapeutic strategies to target OPN.
引用
收藏
页码:2037 / 2044
页数:8
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