The expression of major histocompatibility complex (MHC) class I antig
ens was studied in five breast carcinoma cell lines before and after t
reatment with 17-beta estradiol. Increased HLA class I antigen express
ion correlated with the presence of estrogen receptors. The modulation
of expression appeared to be mediated by transcriptional mechanisms,
as revealed by class I mRNA levels. To elucidate the basis of MHC clas
s I upregulation, we examined transcriptional factor binding activity
to the class I regulatory element (CRE). Our results showed that 17-be
ta estradiol induced increases in factor binding activity to the CRE I
I probe, and decreases to the CRE I probe. In addition, our results su
ggested that factors that bind the CRE I region may modulate the bindi
ng of CRE II. Binding to CRE II was significantly increased in extract
s pretreated with a competitor that contained the CRE I sequence, and
that bound NF-kB/kBF1. In addition, induction of NF-kB binding activit
y by the tumor necrosis factor was accompanied by a decrease in nuclea
r factors that bind to the CRE II region.