Morphologic and biologic studies were undertaken to clarify the biolog
ic significance of basic fibroblast growth factor (bFGF) in human thyr
oid neoplasms. A total of 71 malignant tumors (50 papillary carcinomas
, 14 follicular carcinomas, 7 anaplastic carcinomas), 11 follicular ad
enomas, 6 adenomatous goiters, and 6 Graves' disease tissues were exam
ined employing immunohistochemical methods (avidin-biotin-peroxidase c
omplex technique). An affinity-purified polyclonal rabbit antiserum to
human bFGF was used as a primary antibody. The eluate of malignant th
yroid tumor tissues from the heparin-Sepharose column was examined by
Western blot analysis to elucidate the molecular weight form. With imm
unohistochemical staining, bFGF was frequently detected in the cytopla
sm of malignant thyroid tumors compared to tissues of the benign disea
ses and normal controls. With anaplastic carcinoma, immunoreactivity o
f the tumor cells was particularly strong. In the correlative analyses
between UICC TNM classification and bFGF staining in papillary carcin
oma, there were significant differences when relating positive stainin
g to the grade of nodal metastases. By Western blot analysis, the bFGF
immunoreactivity was specifically detected in the two forms, with mol
ecular weights of 18 and 33 kDa. The high-molecular weight form was de
tected in only anaplastic carcinoma. The present investigations demons
trated a close correlation between the expression of bFGF and the degr
ee of malignancy. bFGF might play an important role in promoting lymph
node metastases. Moreover, the high-molecular-weight form of bFGF mig
ht have an intense influence on tumor growth.