S. Boisnic et al., ALTERATION OF CYTOKERATIN EXPRESSION IN ORAL LICHEN-PLANUS, Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, 79(2), 1995, pp. 207-215
Citations number
35
Categorie Soggetti
Pathology,Surgery,"Dentistry,Oral Surgery & Medicine
The purpose of this investigation is to examine the possible biochemic
al and topographic cytokeratin alterations in lichen planus of oral mu
cosa. Biopsy samples of clinically normal buccal mucosa (n = 5), norma
l gingiva (n = 5), lichen planus from buccal mucosa (n = 5), and liche
n planus from gingiva (n = 5) were obtained from patients of both sexe
s. Cytokeratin expression was determined by means of immunohistochemic
al labeling with use of a battery of monoclonal antibodies against cyt
okeratins and filaggrin and two-dimensional gel electrophoresis. In bu
ccal mucosa, which is not keratinized, cytokeratins 4 and 13 are expre
ssed in the majority. In buccal mucosa lichen planus, the appearance o
f cytokeratins 1, 2, 10, and 11 coincides with a decrease in cytokerat
ins 4 and 13 and a moderate increase in cytokeratins 6, 16, 17, and 19
. In normal gingiva, which is normally keratinized, the main cytokerat
ins are 1, 2, 10, and 11. In gingival lichen planus, a slight decrease
in these cytokeratins and in cytokeratin 13 expression was noted. Fin
ally, alterations in cytokeratins 5 and 14, explained by marked altera
tions of basal cells, were observed. The battery of antibodies used in
this study, in correlation with two-dimensional gel electrophoresis,
could represent useful diagnostic tools that enable the distinction be
tween inflammatory keratosis and so-called quiescent lichen planus. Mo
reover, this work showed that cytokeratins 1, 2, 10, and 11 and filagg
rin are sensitive tools that may help detect early relapse before clin
ical exacerbation. Finally, these biochemical techniques may be useful
to follow the evolution of lichen planus under treatment.