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Differential cadherin expression: potential markers for epithelial to mesenchymal transformation during tumor progression.
Agiostratidou, Georgia; Hulit, James; Phillips, Greg R; Hazan, Rachel B.
Afiliação
  • Agiostratidou G; Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
J Mammary Gland Biol Neoplasia ; 12(2-3): 127-33, 2007 Sep.
Article em En | MEDLINE | ID: mdl-17564818
ABSTRACT
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.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Caderinas / Células Epiteliais / Mesoderma / Neoplasias Limite: Animals / Humans Idioma: En Revista: J Mammary Gland Biol Neoplasia Ano de publicação: 2007 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Caderinas / Células Epiteliais / Mesoderma / Neoplasias Limite: Animals / Humans Idioma: En Revista: J Mammary Gland Biol Neoplasia Ano de publicação: 2007 Tipo de documento: Article