The following article requires a subscription:



(Format: HTML, PDF)

Oestrogen exerts its influence on target organs through activating oestrogen receptors (ERs) and regulating downstream genes by means of their oestrogen-responsive elements. Efp, a target gene product of ER[alpha] 1-3, is a member of the RING-finger B-box coiled-coil (RBCC) motif family 4. Efp is predominantly expressed in various female organs 2 as well as in breast cancers 5, and is thought to be essential for oestrogen-dependent cell proliferation and organ development-Efp-disrupted mice display underdeveloped uteri and reduced oestrogen responsiveness 6. Here we show that Efp is a RING-finger-dependent ubiquitin ligase (E3) that targets proteolysis of 14-3-3[sigma], a negative cell cycle regulator that causes G2 arrest (7). We demonstrate that tumour growth of breast cancer MCF7 cells implanted in female athymic mice is reduced by treatment with antisense Efp oligonucleotide. Efp-overexpressing MCF7 cells in ovariectomized athymic mice generate tumours in the absence of oestrogen. Loss of Efp function in mouse embryonic fibroblasts results in an accumulation of 14-3-3[sigma], which is responsible for reduced cell growth. These data provide an insight into the cell-cycle machinery and tumorigenesis of breast cancer by identifying 14-3-3[sigma] as a target for proteolysis by Efp, leading to cell proliferation.

(C) 2002 Nature Publishing Group