K. Yoshikawa et al., BIOCHEMICAL AND IMMUNOHISTOCHEMICAL ANALYSES OF KERATIN EXPRESSION INBASAL-CELL CARCINOMA, Journal of dermatological science, 17(1), 1998, pp. 15-23
Recently we demonstrated that the keratin 17 (K17) content exceeded th
e K16 content in most follicular tumors, in comparison with non-follic
ular epithelial skin rumours by two-dimensional gel electrophoresis (2
-DE), densitometry and immunohistochemistry. At present the origin of
basal cell carcinoma (BCC) is unknown. So, based on the above results,
we studied keratin expression in eight cases of BCC, in order to anal
yze tumor differentiation by both biochemical and immunohistochemical
methods. Biochemically, using 2-DE and immunoblotting, stratified epit
helial keratins K5/K14 and large amounts of K17 were present in all ca
ses. Simple epithelial keratins K8 and K19 were expressed in all and h
alf of the cases, respectively. However, hyperproliferative associated
keratins (K6/K16) and keratinized keratins (K1/K10) were detected in
only a few cases. Immunohistochemical studies using frozen sections wi
th chain-specific antikeratin monoclonal antibodies against K1, K7, K8
, K10, K14, K16, K17, K18 and K19 showed that BCC tumor cells reacted
positively with antibodies against K8, K14, K17 and K19, but did not r
eact, or were rarely positive with K1, K7, K10, K16 and K18 antibodies
. Predominant expression of K17 and the frequent expression of K8 and
K19, with little K6/K16 and K1/K10 expression are the characteristic f
eatures of BCC, suggesting that BCC is differentiated towards undiffer
entiated follicular epithelia, most probably hair bulge cells. (C) 199
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