Identification of a region of the fibrin molecule involved in upregulation of interleukin-8 expression from human oral squamous cell carcinoma cells
| Autor: | Rajesh V. Lalla, Marvin L. Tanzer, Donald L. Kreutzer |
|---|---|
| Rok vydání: | 2003 |
| Předmět: |
Male
Macromolecular Substances Angiogenesis medicine.drug_class Monoclonal antibody Fibrin Fibrin Fibrinogen Degradation Products Structure-Activity Relationship Downregulation and upregulation In vivo Tumor Cells Cultured medicine Humans Interleukin 8 General Dentistry Aged Dose-Response Relationship Drug biology Chemistry Interleukin-8 Cell Biology General Medicine Molecular biology Peptide Fragments In vitro Up-Regulation Otorhinolaryngology Carcinoma Squamous Cell biology.protein Mouth Neoplasms Cell activation Oligopeptides |
| Zdroj: | Archives of Oral Biology. 48:263-271 |
| ISSN: | 0003-9969 |
| Popis: | A number of studies have implicated the fibrin-coagulation-fibrinolysis system in human tumour progression. Interleukin-8 (IL-8) mediates most of the angiogenic activity induced by human oral squamous cell carcinoma (OSCC) cells. We have recently demonstrated that: (1) fibrin is present in association with IL-8 expressing human OSCC cells in vivo and (2) in situ fibrin polymerisation induces a specific, dose and time-dependent upregulation of IL-8 expression from human OSCC cells in vitro. Our present studies extend this observation by demonstrating that in addition to fibrin formed in situ, both fibrin-derived liquid expressates (soluble fibrin) and preformed fibrin clots induced an over eight-fold stimulation of IL-8 expression from human OSCC cells as compared to media controls. IL-8 upregulation by soluble fibrin was dose-dependent. A monoclonal antibody against the N terminal region of the beta chain of human fibrin (Bbeta15-42) inhibited 67% of soluble fibrin-induced IL-8 expression from human OSCC cells. A peptide (GHRP), representing the sequence at the N terminus of this region, induced a dose-dependent stimulation of IL-8 expression, further confirming the role of this region. These studies directly support our hypothesis that fibrin induces protumourigenic factor expression from tumour cells, thus promoting tumour progression. Future studies to further characterise the role of the Bbeta15-42 region in tumour cell activation may lead to the design of peptide antagonists with important therapeutic potential. |
| Databáze: | OpenAIRE |
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