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ENVIRONMENTAL MODULATION OF α v , α 2 AND β 1 INTEGRIN SUBUNIT EXPRESSION IN HUMAN OESOPHAGEAL SQUAMOUS CELL CARCINOMAS
Author(s) -
Miller Sharon E.,
Veale Rob B.
Publication year - 2001
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1006/cbir.2000.0678
Subject(s) - integrin , cell adhesion molecule , cell , cell adhesion , g alpha subunit , cancer research , biology , ectopic expression , alpha (finance) , phenotype , angiogenesis , microbiology and biotechnology , protein subunit , cell culture , medicine , genetics , construct validity , nursing , gene , patient satisfaction
Integrins are cell adhesion molecules pivotal in regulating normal cell behaviour. Ectopic expression of integrins, characteristic of transformed cells, is instrumental in differentiation, proliferation, apoptosis, angiogenesis, matrix degradation and migration. Oesophageal squamous cell carcinoma (SCC) has a propensity to metastasize and hence an extremely poor prognosis. It is shown here that oesophageal SCCs express α v strongly and that normal oesophageal tissue does not express α v . This makes α v a significant indicator of the transformed phenotype. α 2 and β 1 integrin subunits are down‐regulated in oesophageal SCCs compared to normal oesophagus. Dominance of the α 2 β 1 heterodimer is symptomatic of potential loss of other β 1 binding integrins in oesophageal SCCs. These results suggest a decrease in rigid cell adhesion possibly increasing migratory potential, whilst simultaneously permitting the adhesion and migration of SCC cells on a large repertoire of ligands due to de novo α v expression.