Publication Date:
2002-03-30
Description:
Selective estrogen receptor modulators (SERMs) mimic estrogen action in certain tissues while opposing it in others. The therapeutic effectiveness of SERMs such as tamoxifen and raloxifene in breast cancer depends on their antiestrogenic activity. In the uterus, however, tamoxifen is estrogenic. Here, we show that both tamoxifen and raloxifene induce the recruitment of corepressors to target gene promoters in mammary cells. In endometrial cells, tamoxifen, but not raloxifene, acts like estrogen by stimulating the recruitment of coactivators to a subset of genes. The estrogen-like activity of tamoxifen in the uterus requires a high level of steroid receptor coactivator 1 (SRC-1) expression. Thus cell type- and promoter-specific differences in coregulator recruitment determine the cellular response to SERMs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shang, Yongfeng -- Brown, Myles -- CA57374/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2002 Mar 29;295(5564):2465-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Adult Oncology, Dana-Farber Cancer Institute, 44 Binney Street, and Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11923541" target="_blank"〉PubMed〈/a〉
Keywords:
Breast/*drug effects/metabolism
;
Breast Neoplasms/genetics/metabolism
;
Cell Cycle
;
DNA-Binding Proteins/metabolism
;
Endometrial Neoplasms/genetics/metabolism
;
Endometrium/*drug effects/metabolism
;
Estradiol/pharmacology
;
Female
;
Gene Expression Regulation/drug effects
;
Gene Silencing
;
Genes, myc
;
Histone Acetyltransferases
;
Histone Deacetylases/metabolism
;
Humans
;
Insulin-Like Growth Factor I/genetics
;
Nuclear Receptor Coactivator 1
;
Organ Specificity
;
Promoter Regions, Genetic
;
Raloxifene Hydrochloride/metabolism/*pharmacology
;
Receptors, Estrogen/chemistry/metabolism
;
Repressor Proteins/metabolism
;
Response Elements
;
Selective Estrogen Receptor Modulators/metabolism/*pharmacology
;
Tamoxifen/metabolism/*pharmacology
;
Transcription Factors/genetics/*metabolism
;
Transcription, Genetic
;
Tumor Cells, Cultured
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
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