Matrikine and matricellular regulators of EGF receptor signaling on cancer cell migration and invasion

被引:38
作者
Grahovac, Jelena [1 ]
Wells, Alan [1 ]
机构
[1] Univ Pittsburgh, Dept Pathol, Pittsburgh VAMC, 3550 Terrace St, Pittsburgh, PA 15261 USA
关键词
amoeboid; cancer invasion; decorin; EGFR; mesenchymal; migration; tenascin C; EPIDERMAL-GROWTH-FACTOR; PLASMINOGEN-ACTIVATOR INHIBITOR-1; SPARC-INDUCED MIGRATION; UNSPLICED TENASCIN-C; ACTIN STRESS FIBERS; EXTRACELLULAR-MATRIX; IN-VITRO; GENE-EXPRESSION; FOCAL ADHESIONS; PROTEOGLYCANS BIGLYCAN;
D O I
10.1038/labinvest.2013.132
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cancer invasion is a complex process requiring, among other events, extensive remodeling of the extracellular matrix including deposition of pro-migratory and pro-proliferative moieties. In recent years, it has been described that while invading through matrices cancer cells can change shape and adapt their migration strategies depending on the microenvironmental context. Although intracellular signaling pathways governing the mesenchymal to amoeboid migration shift and vice versa have been mostly elucidated, the extracellular signals promoting these shifts are largely unknown. In this review, we summarize findings that point to matrikines that bind specifically to the EGF receptor as matricellular molecules that enable cancer cell migrational plasticity and promote invasion.
引用
收藏
页码:31 / 40
页数:10
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