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Membrane type 1-matrix metalloproteinase expression is regulated by E-cadherin through the suppression of mitogen-activated protein kinase cascade.
- Source :
-
Cancer letters [Cancer Lett] 2000 Sep 01; Vol. 157 (2), pp. 115-21. - Publication Year :
- 2000
-
Abstract
- To elucidate the role of E-cadherin in matrix metalloproteinases (MMPs) expression, we transfected to squamous carcinoma cells with E-cadherin cDNA. HN5 cells and mock-transfected HN5-neo cells expressed proMMP-2 and active MMP-2. E-cadherin-transfected HN5-EC cells produced comparable proMMP-2 but low active MMP-2; and membrane type 1-MMP (MT1-MMP) mRNA declined. Phosphorylated ERK, a marker of mitogen-activated protein (MAP) kinase cascade, also declined in HN5-EC cells. The addition of anti-E-cadherin antibody resulted in the disappearance of these alterations in HN5-EC cells. These results suggest that E-cadherin suppresses MAP kinase cascade and down-regulates MT1-MMP.
- Subjects :
- Blotting, Western
Cadherins genetics
Carcinoma, Squamous Cell enzymology
Cytoskeletal Proteins metabolism
DNA Primers
DNA, Complementary metabolism
Down-Regulation
Fluorescent Antibody Technique
Gene Expression Regulation, Neoplastic
Humans
Matrix Metalloproteinase 1 biosynthesis
Matrix Metalloproteinase 1 genetics
Matrix Metalloproteinase 2 biosynthesis
Matrix Metalloproteinase 2 genetics
Precipitin Tests
RNA, Messenger metabolism
Reverse Transcriptase Polymerase Chain Reaction
Tissue Inhibitor of Metalloproteinase-2 metabolism
Transfection
Tumor Cells, Cultured
alpha Catenin
beta Catenin
Cadherins metabolism
Carcinoma, Squamous Cell metabolism
MAP Kinase Signaling System
Matrix Metalloproteinase 1 metabolism
Matrix Metalloproteinase 2 metabolism
Mitogen-Activated Protein Kinases metabolism
Trans-Activators
Subjects
Details
- Language :
- English
- ISSN :
- 0304-3835
- Volume :
- 157
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Cancer letters
- Publication Type :
- Academic Journal
- Accession number :
- 10936671
- Full Text :
- https://doi.org/10.1016/s0304-3835(00)00494-8