In this paper we investigated how the increase of human estrogen receptor alfa (ERα) gene expression may affect breast, osteoblast and osteoclast cells. Increase of ERα expression was obtained by interfering with the activity of a negative transcription factor and by removing it with a short and powerful decoy oligonucleotide (RA4-3 ) mimicking a region of distal promoter C of ERα gene. We provide evidence that this decoy was able to induce apoptosis in osteoclasts, but not in osteoblasts and in breast cancer cells, in an estrogen dependent manner. This effect was associated with increase of the levels of Caspase 3 and Fas receptor. Since ERα is important in the transcription of different genes and is involved in several pathological processes, including neoplastic and osteopenic diseases, our findings may be of relevance for a possible new therapeutical approach of such diseases.
Induction of apoptosis of human primary osteoclasts treated with a transcription factor decoy mimicking a promoter region of estrogen receptor alpha
PIVA, Maria Roberta;PENOLAZZI, Maria Letizia;LAMBERTINI, Elisabetta;GIORDANO, Silvia;GAMBARI, Roberto
2005
Abstract
In this paper we investigated how the increase of human estrogen receptor alfa (ERα) gene expression may affect breast, osteoblast and osteoclast cells. Increase of ERα expression was obtained by interfering with the activity of a negative transcription factor and by removing it with a short and powerful decoy oligonucleotide (RA4-3 ) mimicking a region of distal promoter C of ERα gene. We provide evidence that this decoy was able to induce apoptosis in osteoclasts, but not in osteoblasts and in breast cancer cells, in an estrogen dependent manner. This effect was associated with increase of the levels of Caspase 3 and Fas receptor. Since ERα is important in the transcription of different genes and is involved in several pathological processes, including neoplastic and osteopenic diseases, our findings may be of relevance for a possible new therapeutical approach of such diseases.I documenti in SFERA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.