Decorin A Guardian from the Matrix

被引:246
作者
Neill, Thomas [1 ]
Schaefer, Liliana [2 ]
Iozzo, Renato V. [1 ]
机构
[1] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[2] Goethe Univ Frankfurt, Frankfurt, Germany
关键词
GROWTH-FACTOR RECEPTOR; LEUCINE-RICH PROTEOGLYCANS; FACTOR-I RECEPTOR; CANCER GROWTH; BETA-CATENIN; C-MET; BIGLYCAN; EXPRESSION; BINDS; ACTIVATION;
D O I
10.1016/j.ajpath.2012.04.029
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Decorin, an archetypal member of the small leucine-rich proteoglycan gene family, has a broad binding repertoire that encompasses matrix structural components, such as collagens, and growth factors, particularly those that belong to the transforming growth factor-beta ligand superfamily. Within the tumor microenvironment, stromal decorin has an inherent proclivity to directly bind and down-regulate several receptor tyrosine kinases, which are often overexpressed in cancer cells. The decorin interactome commands a powerful antitumorigenic signal by potently repressing and attenuating tumor cell proliferation, survival, migration, and angiogenesis. This collection of interacting molecules also regulates key downstream signaling processes indirectly via the sequestration of growth factors or directly via the antagonism of receptor tyrosine kinases. We propose that decorin can be considered a "guardian from the matrix" because of its innate ability to oppose protumorigenic cues. (Am J Pathol 2012, 181:380-387; http://dx.doi.org/10.1016/j.ajpath.2012.04.029)
引用
收藏
页码:380 / 387
页数:8
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