Abstract |
This study examined the expression of fibroblast growth factor receptor 2 (FGFR 2) splice variants, IIIb and IIIc, in normal and malignant human oral keratinocytes and in normal oral fibroblasts by RT-PCR using both exon-specific primers and primers common to both FGFR 2 isoforms. Fibroblasts expressed exclusively FGFR 2/IIIc whilst the normal and malignant keratinocytes co-expressed FGFR 2/IIIb and FGFR 2/IIIc. Well-differentiated keratinocytes expressed proportionally more FGFR 2/IIIb than IIIc whereas the poorly-differentiated cells expressed more FGFR 2/IIIc than IIIb. The normal and malignant keratinocytes, but not fibroblasts, expressed an additional amplification product, which consisted of both IIIb and IIIc of FGFR 2 joined by an extra base pair and with the intronic sequence removed. The results indicate that the expression of FGFR 2 isoforms reflects the degree of cellular differentiation in normal and malignant human oral keratinocytes and that receptor complexes of FGFR 2/IIIb and IIIc may regulate ligand-receptor interactions.
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Authors | C S Drugan, I C Paterson, S S Prime |
Journal | Carcinogenesis
(Carcinogenesis)
Vol. 19
Issue 6
Pg. 1153-6
(Jun 1998)
ISSN: 0143-3334 [Print] England |
PMID | 9667757
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Receptors, Fibroblast Growth Factor
- FGFR2 protein, human
- Receptor Protein-Tyrosine Kinases
- Receptor, Fibroblast Growth Factor, Type 2
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Topics |
- Carcinoma, Squamous Cell
(genetics, pathology)
- Cell Differentiation
(genetics)
- Exons
- Humans
- Mouth Neoplasms
(genetics, pathology)
- Polymerase Chain Reaction
- RNA Splicing
- Receptor Protein-Tyrosine Kinases
(genetics)
- Receptor, Fibroblast Growth Factor, Type 2
- Receptors, Fibroblast Growth Factor
(genetics)
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