Journal
ONCOGENE
Volume 21, Issue 18, Pages 2854-2863Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.onc.1205386
Keywords
aromatase; gene regulation; nuclear receptors; breast cancer
Funding
- NCI NIH HHS [CA65767, CA44735] Funding Source: Medline
- NIEHS NIH HHS [ES08258] Funding Source: Medline
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Using the yeast one-hybrid approach to screen a human breast tissue hybrid cDNA expression library, we have found that four orphan/nuclear receptors, ERRalpha-1, EAR-2, COUP-TFI (EAR-3), and RARgamma, bind to the silencer (SI) region of the human aromatase gene. S1 down regulates promoters 1.3 and 11 of the human aromatase gene. In this study, the interaction of EAR-2, COUP-TFI, and RARgamma with SI was confirmed by DNA mobility shift analysis. In contrast to the findings that ERRalpha-1 behaves as a positive regulatory factor, these three nuclear receptors were found, by, mammalian cell transfection experiments, to act as negative regulatory factors by binding to SI. Furthermore, the negative action of these three nuclear receptors could override the positive effect of ERRalpha-1. RT-PCR analysis of 11 cell lines and 55 human breast tumor specimens has shown that these nuclear receptors are expressed in human breast tissue. Since EAR-2, COUP-TFI, and RARgamma are expressed at high levels, it is likely that SI is a negative regulatory element that suppresses aromatase promoters 1.3 and 11 in normal breast tissue. In cancer tissue, SI may function as a positive element since ERRYalpha-1 is expressed, but EAR-2 and RARgamma are only present in a small number of tumor specimens. This hypothesis is sustained by the finding that there is a weak inverse correlation between the expression of COUP-TFI and that of aromatase in breast tumor tissue. Our studies have revealed that estrogen receptor alpha (ERalpha) can also bind to SI, in a ligand-dependent manner. By binding to S1, ERalpha down-regulates the aromatase promoter activity. These results demonstrate that nuclear receptors play important roles in modulating aromatase expression in human breast tissue.
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