Two antiestrogens affect differently chromatin remodeling of trefoil factor 1 (pS2) gene and the fate of estrogen receptor in MCF7 cells

This publication has 19 references indexed in Scilit:

• The Human Estrogen Receptor-α Is a Ubiquitinated Protein Whose Stability Is Affected Differentially by Agonists, Antagonists, and Selective Estrogen Receptor Modulators
  Journal of Biological Chemistry, 2001
• The 26S Proteasome Is Required for Estrogen Receptor-α and Coactivator Turnover and for Efficient Estrogen Receptor-α Transactivation
  Molecular Cell, 2000
• Subnuclear Trafficking of Estrogen Receptor- and Steroid Receptor Coactivator-1
  Molecular Endocrinology, 2000
• Comparative Analyses of Mechanistic Differences Among Antiestrogens
  Endocrinology, 1999
• Chromatin structure of the regulatory regions of pS2 and cathepsin D genes in hormone-dependent and -independent breast cancer cell lines
  Oncogene, 1999
• Interaction and Dissociation by Ligands of Estrogen Receptor and Hsp90: The Antiestrogen RU 58668 Induces a Protein Synthesis-Dependent Clustering of the Receptor in the Cytoplasm
  Molecular Endocrinology, 1998
• Synthetic antiestrogens modulate induction of pS2 and cathepsin-D messenger ribonucleic acid by growth factors and adenosine 3',5'- monophosphate in MCF7 cells
  Endocrinology, 1993
• Structural differences between the hormone and antihormone estrogen receptor complexes bound to the hormone response element.
  Proceedings of the National Academy of Sciences, 1991
• Estrogen-responsive element of the human pS2 gene is an imperfectly palindromic sequence.
  Proceedings of the National Academy of Sciences, 1989
• A rapid, sensitive, and specific method for the determination of protein in dilute solution
  Analytical Biochemistry, 1973