METALLOTHIONEIN EXPRESSION IN NORMAL, HYPERPLASTIC, AND NEOPLASTIC THYROID FOLLICULAR AND PARAFOLLICULAR C-CELLS USING MONOCLONAL ANTIMETALLOTHIONEIN ANTIBODY-E9
Kw. Schmid et al., METALLOTHIONEIN EXPRESSION IN NORMAL, HYPERPLASTIC, AND NEOPLASTIC THYROID FOLLICULAR AND PARAFOLLICULAR C-CELLS USING MONOCLONAL ANTIMETALLOTHIONEIN ANTIBODY-E9, Endocrine pathology, 5(2), 1994, pp. 114-122
Metallothioneins (MTS) are a set of ubiquitous low molecular proteins
with a high affinity for metal ions, such as zinc, copper, and cadmium
. MT overexpression can be induced by these metal ions as well as by o
ther endogenous and exogenous factors. In this study, normal, hyperpla
stic, and neoplastic thyroid tissues of both follicular and C-cell ori
gin were immunohistochemically investigated with a monoclonal antibody
against I- and II-isoforms of MTs. MT immunoreactivity was demonstrat
ed in the follicular epithelium of 19 normal thyroid glands and in all
32 cases of Graves' disease investigated; 26 of 30 follicular adenoma
s and 25 of 28 follicular carcinomas showed MT immunoreactivity, where
as only 7 of 20 papillary carcinomas were MT-positive (p < 0.0001). In
3 of the 7 positive samples, positivity was restricted to follicular
areas of differentation. No MT could be immunolocalized in normal and
hyperplastic C cells and medullary thyroid carcinomas (n = 20). In mix
ed medullary-follicular carcinomas (n = 4), MT staining patterns resem
bled those seen for thyroglobulin. In anaplastic carcinomas, MTs were
mainly immunolocalized in nonspindle cell areas. MT expression in thyr
oid tumors may reflect the different biological behavior of follicular
and papillary carcinomas. Antibodies to MTs may also serve as fairly
specific immunohistochemical markers of follicular cell differentiatio
n in thyroid neoplasia.