Tyrosine kinases (TKs) are important candidate genes for malignant transfor
mation and at least 21 different TKs have been identified in the thyroid gl
and. We hypothesized that the collective activity of these TKs might be inc
reased in thyroid carcinoma and have association with the clinical behavior
of individual tumors. To test this, we determined TK expression by immunoh
istochemistry in 74 archival thyroid tissue blocks (48 papillary thyroid ca
rcinoma, PTC; 9 follicular thyroid carcinoma, FTC; 17 benign thyroid diseas
es) from children and young adults. Mean TK expression was greater for PTC
(2.1 +/- 0.11) than benign lesions (1.6 +/- 0.2, p = 0.027), and also tende
d to be greater in ETC (2.1 +/- 0.25, p = 0.12). Recurrence risk was three-
fold greater for PTC with intense TK expression (4/15, 27%) than for PTC wi
th minimal - moderate TK expression (3/33, 9.0%). However, this was not sta
tistically significant (p = 0.10). In PTC, TK expression correlated with ex
pression of the receptor for hepatocyte growth factor/scatter factor (cMET,
r = 0.31, p = 0.044). In FTC, TK expression did not correlate with cMET, b
ut tended to be greater in young patients (r= -0.59, p = 0.09). We conclude
that TK expression is increased in PTC and possibly associated with an inc
reased recurrence risk.