Gr. Ogden et al., INFLUENCE OF TEMPERATURE ON LONG-TERM KERATIN IMMUNOREACTIVITY FOR ORAL EXFOLIATIVE, Analytical and quantitative cytology and histology, 17(1), 1995, pp. 35-38
We previously showed that keratin profiles can be of value in the diag
nosis of oval cancer when using exfoliative cytology. In the future, t
hey may form part of a screening program for oral cancer. This study e
valuated the influence of long-term storage on keratin expression. Sme
ars were collected from the clinically normal buccal mucosa and dorsal
tongue of 22 patients. Half were stored in a refrigerator (5 degrees
C) and half in a freezer (-70 degrees C). A fetal of 528 smears were c
ollected. A panel of three antikeratin antibodies (LP34, AE8 and 1C7)
wits used to identify the preservation of keratin expression (graded a
s absent, few cells positive or many cells positive). The results for
smears from dorsal tongue indicated that many cells were impermeable b
y the antikeratin antibodies. However, a satisfactory level of keratin
immunoreactivity teas observed in smears from buccal mucosa stored at
-70 degrees C for over one year. Results for storage at 5 degrees C f
or both sites were inadequate after one month. Thus, smears from nonke
ratinized oral sites may be stored at -70 degrees C for at least one y
ear without a profound loss of keratin immunoreactivity, thus allowing
examination of archival material.