Perspectives in Pharmacology Molecular Mechanisms of Selective Estrogen Receptor Modulator (SERM) Action1

In females, estrogens play a key role in reproduction and have beneficial effects on the skeletal, cardiovascular, and central nervous systems. Most estrogenic responses are mediated by estrogen receptors (ERs), either ERa or ERb, which are mem-bers of the nuclear receptor superfamily of ligand-dependent transcription factors. Selective estrogen receptor modulators (SERMs) are ER ligands that in some tissues act like estrogens, but block estrogen action in others. Thus, SERMs may exhibit an agonistic or antagonistic biocharacter depending on the context in which their activity is examined. For example, the SERMs tamoxifen and raloxifene both exhibit ER antagonist activity in breast and agonist activity in bone, but only tamox-ifen manifests agonist activity in the uterus. Numerous studies have examined the molecular basis for SERM selectivity. Col-lectively they indicate that different ER ligands induce distinct structural changes in the receptor that influence its ability to interact with other proteins (e.g., coactivators or corepressors) critical for the regulation of target gene transcription. The rela-tive expression of coactivators and corepressors, and the na-ture of the ER and of its target gene promoter affect SERM biocharacter. Taken together, SERM selectivity reflects the di-versity of ER forms and coregulators, cell type differences in their expression, and the diversity of ER target genes. This model provides a basis for understanding the molecular mech-anisms of SERM action, and should help identify new SERMs with enhanced tissue or target gene selectivity