Jw. Huang et al., IMMUNOHISTOCHEMICAL EVALUATION OF THE CA2-BINDING S-100 PROTEINS S-100A1, S-100A2, S-100A4, S-100A6 AND S-100B IN SALIVARY-GLAND TUMORS(), Journal of oral pathology & medicine, 25(10), 1996, pp. 547-555
The Ca2+-binding S-100 proteins are involved in the regulation of a nu
mber of cellular processes and an altered expression has been reported
in several neoplastic tissues. Tissue specimens of normal salivary gl
ands (n=23), pleomorphic adenomas (n=60), basal cell adenomas (n=6), c
analicular ademomas (n=2), myoepitheliomas (n=2), adenoid cystic carci
nomas (n=26) and adenocarcinomas NOS (n=11) were evaluated for the exp
ression of S-100A1, S-100A2, A-100A4, S-100A6 and S-100B by using high
ly specific polyclonal and monoclonal antibodies generated against the
recombinant human protein. In normal salivary glands, the ductal cell
s showed mild to intense immunoreactivity for S-100A1, S-100A2, S-100A
4 and S-100A6, while S-100B was observed in nerve fibers in the connec
tive tissue. The normal myoepithelial cells were unreactive. In pleomo
rphic adenoma, the luminal tumor cells of the duct-like structures sho
wed moderate to intense immunoreactivity for S-100A2, while reactivity
for S-100A1, S-100A4 and S-100A6 was relatively weak. The non-luminal
cells, also termed neoplastic myoepithelial cells, showed immunoreact
ivity for S-100B, while tumor cells in the solid, myxoid and chondroid
areas were immunoreactive for S-100A1, S-100A4, S-100A6 and S-100B. T
he non-luminally located tumor cells in basal cell adenomas and canali
cular adenomas, and numerous tumor cells in clusters in myoepithelioma
s were intensely reactive for S-100A2. In adenoid cystic carcinomas an
d in adenocarcinomas not otherwise specified, the luminal cells formin
g the tubular or cribriform structures were markedly positive for S-10
0A2 and/or S-100A6. Squamous metaplastic cells in salivary tumors show
ed intense immunoreactivity for S-100A2. The results of the present st
udy suggest that the majority of the tumor cells in salivary neoplasms
, despite the most heterogeneous tumor cell differentiation, express S
-100 proteins more heterogeneously than the normal glandular ducts. Th
e salivary ducts in normal glands, the luminal tumor cells and squamou
s metaplastic cells in the neoplastic lesions were intensely immunorea
ctive for S-100A2 as compared to S-100A1, S-100A4 or S-100A6. In contr
ast, the non-luminal tumor cells showed a rather heterogeneous express
ion of the S-100 proteins.