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Midkine promotes tetraspanin–integrin interaction and induces FAK-Stat1α pathway contributing to migration/invasiveness of human head and neck squamous cell carcinoma cells
- Source :
- Biochemical and Biophysical Research Communications. 377:474-478
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- The heparin-binding growth factor, MK, promoting tumorigenesis and survival was found to associate with alpha6beta1 integrins. We showed for the first time that MK interacted with TSPAN1 and facilitated the association between TSPAN1 and integrin alpha6beta1 proteins in head and neck squamous cell carcinoma (HNSCC) cells. We found that MK mediated an integrin-dependent tyrosine phosphorylation of FAK and activation of paxillin and Stat1alpha pathways. As result, downstream target genes implicated in cell migration and invasiveness (e.g. MMP-2 and MMP-26) were overexpressed. We observed that RNAi silencing of the critical signaling intermediates led to decrease of MK-induced migration/invasiveness of HNSCC cells. The major finding of this study is a novel MK-triggered signaling mechanism implicated in migration and invasiveness of HNSCC cells.
- Subjects :
- Tetraspanins
Integrin
Biophysics
Gene Expression
Biochemistry
chemistry.chemical_compound
Tetraspanin
Cell Movement
Two-Hybrid System Techniques
medicine
Humans
Neoplasm Invasiveness
Nerve Growth Factors
Molecular Biology
Paxillin
Midkine
Integrin alpha6beta1
biology
Chemistry
Membrane Proteins
Cell migration
Tyrosine phosphorylation
Interferon-Stimulated Gene Factor 3
Cell Biology
medicine.disease
Head and neck squamous-cell carcinoma
Head and Neck Neoplasms
Focal Adhesion Kinase 1
Carcinoma, Squamous Cell
biology.protein
Cancer research
RNA Interference
Signal transduction
Genes, Neoplasm
Signal Transduction
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 377
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....d9e0c79274b388f2c2b08554c86f2110
- Full Text :
- https://doi.org/10.1016/j.bbrc.2008.09.138