Differential cadherin expression: Potential markers for epithelial to mesenchymal transformation during tumor progression

被引:77
作者
Agiostratidou, Georgia
Hulit, James
Phillips, Greg R.
Hazan, Rachel B.
机构
[1] Albert Einstein Coll Med, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10461 USA
[3] CUNY Mt Sinai Sch Med, Fishberg Dept Neurosci, New York, NY 10029 USA
关键词
adhesion; metastasis; breast cancer; signaling; invasion;
D O I
10.1007/s10911-007-9044-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The cadherin family of adhesion molecules regulates cell-cell interactions during development and in tissues. The prototypical cadherin, E-cadherin, is responsible for maintaining interactions of epithelial cells and is frequently downregulated during tumor progression. N-cadherin, normally found in fibroblasts and neural cells, can be upregulated during tumor progression and can increase the invasiveness of tumor cells. The proinvasive effects of N-cadherin expression in tumor cells result from two possible mechanisms: promotion of tumor cell interactions with the N-cadherin-expressing microenvironment, or enhancement of signaling via the fibroblast growth factor receptor. The downregulation of E-cadherin and the upregulation of N-cadherin in tumors may be a result of an epithelial to mesenchymal transformation (EMT) of tumor cells, which is notoriously difficult to detect in vivo. Double labeling of individual tumors with specific E- and N-cadherin antibodies suggests that EMT can occur heterogeneously and/or transiently within an invasive tumor.
引用
收藏
页码:127 / 133
页数:7
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