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Literature summary for 3.4.24.B28 extracted from

  • Mattern, J.; Roghi, C.; Hurtz, M.; Knaeuper, V.; Edwards, D.; Poghosyan, Z.
    ADAM15 mediates upregulation of claudin-1 expression in breast cancer cells (2019), Sci. Rep., 9, 12540 .
    View publication on PubMedView publication on EuropePMC

Organism

Organism UniProt Comment Textmining
Homo sapiens Q13444
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Source Tissue

Source Tissue Comment Organism Textmining
MCF-7 cell
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Homo sapiens
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MDA-MB-231 cell
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Homo sapiens
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General Information

General Information Comment Organism
physiological function expression of ADAM15 natural isoforms in MDA-MB-231 cells leads to cell clustering to varying degree, without changes in epithelial mesenchymal transition markers vimentin, slug and E-cadherin. Expression leads to ADAM15 isoform specific, catalytic function dependent upregulation of claudin-1. The expression of ADAM15A, and to a lesser degree of C and E isoforms leads to an increase in claudin-1 expression in MDA-MB-231 cells, while ADAM15B has no effect. In MCF-7 cells, ADAM15E is the principal variant inducing claudin-1 expression. The PI3K/Akt/mTOR pathway is involved in regulating claudin-1 expression downstream of ADAM15. ADAM15 co-localizes with claudin-1 and ZO1 at cell-cell junctions Homo sapiens