It is now widely accepted that human neoplasms arise as a result of a
sequence of mutations affecting the structure of genes involved in gro
wth control. Identifying the nature of such genetic mutations in thyro
id neoplasms and their prevalence in the various tumor phenotypes is c
ritical to the understanding of their pathogenesis. Mutational activat
ion of ras oncogenes has been associated with human thyroid neoplasia.
We examined the expression of ras oncogene in benign hyperplastic or
inflamatory lesions of the goiter, as well as in benign and malignant
thyroid tumors. Although no significant differences of ras oncogene ex
pression was found between benign and malignant lesions, the overexpre
ssion in proliferative areas generally suggests the possible involveme
nt of ras oncogene in the trophic hormone control of the thyroid.