Carcinogenesis, Vol 19, 1153-1156, Copyright © 1998 by Oxford University Press
CS Drugan, IC Paterson and SS Prime
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.
ARTICLES
Fibroblast growth factor receptor expression reflects cellular differentiation in human oral squamous carcinoma cell lines
Department of Oral and Dental Science, University of Bristol, UK.
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