Skip Navigation

This Article
Right arrow Print PDF (2323K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (113)
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Cavailles, V.
Right arrow Articles by Rochefort, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cavailles, V.
Right arrow Articles by Rochefort, H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1988, Vol. 16, No. 5 1903-1919
© 1988


Articles

Estrogens and growth factors induce the mRNA of the 52K-pro-cathepsin-D secreted by breast cancer cells

Vincent Cavailles, Patrick Augerau, Marcel Carcia and Henri Rochefort*

Unité d'Endocrinologie Cellulaire et Moléculaire U 148 INSERM, 60, rue de Navacelles, 34100 Montpellier, France

*To whom correspondence should be addressed

Received January 12, 1988. Accepted February 11, 1988.

The estrogen-induced 52K protein secreted by human breast cancer cells is a lysosomal protease recently identified as a pro-cathepsin D by sequencing several cDNA clones isolated from MCF7 cells (Augereau et al., Mol. Endocr.). Using one of these clones, we detected, in MCF7 cells, a 2.2 kb mRNA whose level was rapidly increased 4- to 10-fold by estradlol, but not by other classes of steroids. Other mitogens, such as epidermal growth factor and insulin, also induced the 2.2 kb mRNA in a dose-dependent manner. Induction with epidermal growth factor was as rapid but was 2- to 3-fold lower than with estradiol. Antiestrogens had no effect on the 52K-cathepsin-D mRNA in MCF cells, but became estrogen agonists in two antiestrogen-resistant sublines R27 and LY2. The use of transcription and translation inhibitoi and nuclear run-on experiments indicate that estradiol enhances transcription of the 52K-cathepsin-D gene in MCF7 cells.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol. Endocrinol.Home page
S. Carascossa, J. Gobinet, V. Georget, A. Lucas, E. Badia, A. Castet, R. White, J.-C. Nicolas, V. Cavailles, and S. Jalaguier
Receptor-Interacting Protein 140 Is a Repressor of the Androgen Receptor Activity
Mol. Endocrinol., July 1, 2006; 20(7): 1506 - 1518.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
A. C. Nye, R. R. Rajendran, D. L. Stenoien, M. A. Mancini, B. S. Katzenellenbogen, and A. S. Belmont
Alteration of Large-Scale Chromatin Structure by Estrogen Receptor
Mol. Cell. Biol., May 15, 2002; 22(10): 3437 - 3449.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
Y. Shi, M. Downes, W. Xie, H.-Y. Kao, P. Ordentlich, C.-C. Tsai, M. Hon, and R. M. Evans
Sharp, an inducible cofactor that integrates nuclear receptor repression and activation
Genes & Dev., May 1, 2001; 15(9): 1140 - 1151.
[Abstract] [Full Text]


Home page
J. Cell Biol.Home page
K. Honda, T. Yamada, R. Endo, Y. Ino, M. Gotoh, H. Tsuda, Y. Yamada, H. Chiba, and S. Hirohashi
Actinin-4, a Novel Actin-bundling Protein Associated with Cell Motility and Cancer Invasion
J. Cell Biol., March 23, 1998; 140(6): 1383 - 1393.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.