{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Salazar MD"],"funding":["NCI NIH HHS"],"pagination":["R18"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3109587"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13(1)"],"pubmed_abstract":["<h4>Introduction</h4>Current hormonal adjuvant therapies for breast cancer including tamoxifen treatment and estrogen depletion are overall tumoristatic and are severely limited by the frequent recurrence of the tumors. Regardless of the resistance mechanism, development and progression of the resistant tumors requires the persistence of a basal level of cycling cells during the treatment for which the underlying causes are unclear.<h4>Methods</h4>In estrogen-sensitive breast cancer cells the effects of hormone depletion and treatment with estrogen, tamoxifen, all-trans retinoic acid (ATRA), fulvestrant, estrogen receptor α (ER) siRNA or retinoic acid receptor α (RARα) siRNA were studied by examining cell growth and cycling, apoptosis, various mRNA and protein expression levels, mRNA profi"],"journal":["Breast cancer research : BCR"],"pubmed_title":["During hormone depletion or tamoxifen treatment of breast cancer cells the estrogen receptor apoprotein supports cell cycling through the retinoic acid receptor α1 apoprotein."],"pmcid":["PMC3109587"],"funding_grant_id":["CA 140690"],"pubmed_authors":["Trumbly R","Kisovic I","Iman M","Patki M","Ratnam M","Salazar MD"],"additional_accession":[]},"is_claimable":false,"name":"During hormone depletion or tamoxifen treatment of breast cancer cells the estrogen receptor apoprotein supports cell cycling through the retinoic acid receptor α1 apoprotein.","description":"<h4>Introduction</h4>Current hormonal adjuvant therapies for breast cancer including tamoxifen treatment and estrogen depletion are overall tumoristatic and are severely limited by the frequent recurrence of the tumors. Regardless of the resistance mechanism, development and progression of the resistant tumors requires the persistence of a basal level of cycling cells during the treatment for which the underlying causes are unclear.<h4>Methods</h4>In estrogen-sensitive breast cancer cells the effects of hormone depletion and treatment with estrogen, tamoxifen, all-trans retinoic acid (ATRA), fulvestrant, estrogen receptor α (ER) siRNA or retinoic acid receptor α (RARα) siRNA were studied by examining cell growth and cycling, apoptosis, various mRNA and protein expression levels, mRNA profi","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011 Feb","modification":"2026-04-07T17:53:05.071Z","creation":"2026-04-07T16:09:49.183Z"},"accession":"S-EPMC3109587","cross_references":{"pubmed":["21299862"],"doi":["10.1186/bcr2827"]}}