Expression of squamous cell carcinoma (SCC) antigen emerged concurrently wi
th squamous formation of the uterine cervix and increased during the neopla
stic transformation of the cervical squamous epithelium. SCC antigen expres
sion differed considerably among the histomorphologic cell types of cervica
l carcinoma. Large cell nonkeratinizing carcinoma contained high levels of
the antigen. In contrast, no appreciable expression of SCC antigen was obse
rved in small cell nonkeratinizing carcinoma. The pattern of SCC antigen ex
pression closely coincided with EGF receptor (EGF-R) expression in cervical
squamous neoplasia. This suggests that the expression of SCC and EGF-R in
cervical carcinoma is related to the differentiation or dedifferentiation p
rocesses of the tumor cells. SCC production by CaSki cervical epidermoid ca
rcinoma cells was stimulated by EGF. IL seems likely that an autocrine syst
em, in which EGF serves as the signal, may exist in cervical squamous carci
noma. 17 beta-estradiol and L-triiodothyronine were found to upregulate EGF
-R expression, proliferative potential and SCC production in the CaSki cerv
ical carcinoma cells.