MURAL - Maynooth University Research Archive Library

    Posttranslational Truncation of E-Cadherin and Significance for Tumour Progression

    Masterson, Joanne C. and O'Dea, Shirley (2007) Posttranslational Truncation of E-Cadherin and Significance for Tumour Progression. Cells Tissues Organs, 185. pp. 175-179. ISSN 1422-6405

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    Stable intraepithelial adhesion complexes are essential for the maintenance of epithelial integrity. Alterations in these complexes are key events in the development and progression of many diseases. One of the major proteins involved in maintaining epithelial cell-cell adhesion is the cell-adhesion junction protein E-cadherin, a member of the cadherin family of transmembrane adhesion proteins. E-cadherin is involved in many cellular processes including morphogenesis, adhesion, recognition, communication and oncogenesis. Inactivation of its adhesive properties is often a key step in tumour progression and metastasis, leading to its recent description as a tumour suppressor gene. Mutations of the Ecadherin gene CDH1 in gastric and mammary cancers have been well documented and reports of transcriptional repression during tumour progression are increasing. This review examines the role of posttranslational truncation of Ecadherin in cancer cells focusing on implications for tumour progression. The various proteins involved in the directed cleavage of E-cadherin and consequences of these truncations are discussed.

    Item Type: Article
    Keywords: E-cadherin; E-cadherin truncation; Matrix metallo proteinase; Tumour progression;
    Academic Unit: Faculty of Science and Engineering > Biology
    Faculty of Science and Engineering > Research Institutes > Institute of Immunology
    Item ID: 3056
    Depositing User: Dr. Shirley O'Dea
    Date Deposited: 30 Jan 2012 14:37
    Journal or Publication Title: Cells Tissues Organs
    Publisher: Karger
    Refereed: Yes
      Use Licence: This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available here

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