| Literature DB >> 1993074 |
V Cavailles1, P Augereau, H Rochefort.
Abstract
Cathepsin D is a lysosomal protease produced and secreted in excess by most human breast cancer cells. In MCF7 cells, estrogens stimulate cathepsin D expression at the mRNA level via a mechanism independent of de novo protein synthesis. We have isolated the human cathepsin D gene and its 5' flanking sequences from a MCF7 genomic library. To demonstrate its transcriptional estrogen regulation, we constructed chimeric recombinants bearing different fragments of the cathepsin D gene 5' proximal region inserted in front of the bacterial chloramphenicol acetyl transferase reporter gene. By transient cotransfection with the estrogen receptor expression vector into MCF7 cells, we showed that a 240 bp fragment located in the 5' proximal region of the gene was able to mediate transcriptional estrogen activation. This induction was concentration-dependent and suppressed by the antiestrogen ICI 164, 384.Entities:
Mesh:
Substances:
Year: 1991 PMID: 1993074 DOI: 10.1016/0006-291x(91)91491-t
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575