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Estradiol Regulates Different Genes in Human Breast Tumor Xenografts Compared with the Identical Cells in Culture

Department of Medicine (D.M.E.H., J.K.R., C.A.S., K.B.H.), Division of Endocrinology, and Department of Pathology (K.B.H.), University of Colorado Health Sciences Center at Fitzsimons, Aurora, Colorado 80045; and Breast Center (D.C.A.), Baylor College of Medicine, Houston, Texas 77030

Address all correspondence and requests for reprints to: Djuana M. E. Harvell, Ph.D., University of Colorado Health Sciences Center at Fitzsimons, Endocrinology MS 8106, P.O. Box 6511, Aurora, Colorado 80045. E-mail: djuana.harvell{at}uchsc.edu.

In breast cancers, estrogen receptor (ER) levels are highly correlated with response to endocrine therapies. We sought to define mechanisms of estrogen (E) signaling in a solid breast tumor model using gene expression profiling. ER⁺ T47D-Y human breast cancer cells were grown as xenografts in ovariectomized nude mice under four conditions: 1) 17ß-estradiol for 8 wk (E); 2) without E for 8 wk (control); 3) E for 7 wk followed by 1 wk of E withdrawal (Ewd); or 4) E for 8 wk plus tamoxifen for the last week. E-regulated genes were defined as those that differed significantly between control and E and/or between E and Ewd or control and Ewd. These protocols generated 188 in vivo E-regulated genes that showed two major patterns of regulation. Approximately 46% returned to basal states after Ewd (class I genes); 53% did not (class II genes). In addition, more than 70% of class II-regulated genes also failed to reverse in response to tamoxifen. These genes may be interesting for the study of hormone-resistance issues. A subset of in vivo E-regulated genes appears on lists of clinical ER discriminator genes. These may be useful therapeutic targets or markers of E activity. Comparison of in vivo E-regulated genes with those regulated in identical cells in vitro after 6 and 24 h of E treatment demonstrate only 11% overlap. This indicates the extent to which gene expression profiles are uniquely dependent on hormone-treatment times and the cellular microenvironment.

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