F. Smedts et al., DETECTION OF KERATIN SUBTYPES IN ROUTINELY PROCESSED CERVICAL TISSUE - IMPLICATIONS FOR TUMOR CLASSIFICATION AND THE STUDY OF CERVIX CANCERETIOLOGY, Virchows Archiv, 425(2), 1994, pp. 145-155
We investigated the expression of keratin subtypes 7, 8, 10, 13, 14, 1
7, 18 and 19 in the normal cervix, in cervical intraepithelial neoplas
ia (CIN) lesions and in cervical carcinomas, using a selected panel of
monoclonal keratin antibodies, reactive with routinely processed, for
malin fixed paraffin embedded tissue fragments. The reaction patterns
derived for each keratin antibody were compared with known expression
patterns of the various epithelia, previously examined in frozen tissu
es. Although the reactivity of the antibodies was generally acceptable
, considerable modifications to the manufacturers' staining instructio
ns were often necessary. For some antibodies, which were previously th
ought to be reactive with fresh frozen tissue only, we developed stain
ing protocols rendering them reactive with routinely processed materia
l. As with previous findings in frozen sections we observed increasing
expression of keratins 7, 8, 17, 18 and 19 with increasing grade of C
IN. In cervical carcinomas the differences in keratin detectability be
tween the main categories were more pronounced than in frozen sections
, probably due to fixation and processing. For routine pathology, kera
tin phenotyping of cervical lesions may be of value in classification.
The fact that keratin 7 was detected for the first time in reserve ce
lls, and that this keratin was also found to be expressed in a conside
rable number of CIN lesions and cervical carcinomas supports the sugge
stion that reserve cells are a common progenitor cell for these lesion
s.