Background. The Id-1 helix-loop-helix protein inhibits differentiation and
enhances cell proliferation. It is require for cell cycle progression. The
Id-1 gene is highly expressed in a variety of tumor-derived cell lines. It
increases after mitogen stimulation and is overexpressed in some human neop
lasms. Therefore, we hypothesized that the Id-1 gene may play a rob in medu
lla thyroid carcinogenesis.
Methods, The expression of the Id-1 protein in human medullary thyroid canc
er (MTC) and the corresponding normal thyroid tissue was determined by Id-1
immunohistochemistry. In a human MTC cell line (TT), the effects of growth
stimulation and redifferentiation on Id-1 expression were determined by No
rthern blot analysis.
Results, Id-1 immunostaining intensity in 9 MTC samples (6 sporadic, 2 fami
lial, and 1 MEN 2A) was moderate to strong However, it was absent or faint
in the corresponding normal thyroid tissue. The Id-1 protein was significan
tly overexpressed in MTC compared with corresponding normal thyroid tissue
on the basis of the percentage of positive cells and immunostaining intensi
ty (P =.002). In the TT cell line, Id-1 messenger RNA (mRNA) expression was
increased 4-fold after growth stimulation with serum. Phorbol ester (which
induces redifferentiation in the TT cell line) downregulated Id-1 mRNA exp
ression.
Conclusions. Id-1 is overexpressed in MTC. The Id-1 gene may play a role in
the regulation of MTC differentiation and proliferation.