Structural Determination of Certain Novel ER Complexes
Abstract
Tamoxifen is effective for the prevention and treatment of estrogen-dependent breast cancers, but is associated with an increased incidence of endometrial tumors. We completed the first aim of this proposal to solve the crystal structure of the estrogen receptor alpha ligand-binding domain (ER alpha LBD) bound to the structurally similar compound GW5638, which has therapeutic potential and does not stimulate the uterus. Like tamoxifen, GW5638 relocates the carboxy-terminal helix (H12) to the known coactivator-docking site in the ER alpha LBD. However, GW5638 repositions residues in H12 through specific contacts with the N-terminus of this helix. In contrast to tamoxifen, the resulting increase in exposed hydrophobic surface of ER alpha LBD correlates with a significant degradation of ER alpha in MCF-7 cells. Thus, the GW5638-ER alpha LBD structure reveals a unique mode of SERM-mediated ER antagonism, in which the stability of ER alpha is decreased through an altered position of H12. This dual mechanism of antagonism may explain why GW5638 can inhibit tamoxifen-resistant breast tumors. In addition, difficulties encountered with experiments under aim 2 and 3 were addressed along with alternative approaches proposed in this report.
Document Details
- Document Type
- Technical Report
- Publication Date
- Sep 01, 2004
- Accession Number
- ADA434775
Entities
People
- Geoffrey L Greene
- Ya-ling Wu
Organizations
- University of Chicago