<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Herber CB</submitter><funding>NIA NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>National Institutes of Health</funding><funding>National Institute on Aging</funding><pagination>44</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9036729</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Menopausal hormone therapy (MHT) is recommended for only five years to treat vasomotor symptoms and vulvovaginal atrophy because of safety concerns with long-term treatment. We investigated the ability of 2',3',4'-trihydroxychalcone (2',3',4'-THC) to modulate estrogen receptor (ER)-mediated responses in order to find drug candidates that could potentially prevent the adverse effects of long-term MHT treatment.&lt;h4>Methods&lt;/h4>Transfection assays, real time-polymerase chain reaction, and microarrays were used to evaluate the effects of 2',3',4'-THC on gene regulation. Radioligand binding studies were used to determine if 2',3',4'-THC binds to ERα. Cell proliferation was examined in MCF-7 breast cancer cells by using growth curves and flow cytometry. Western blots were used</pubmed_abstract><journal>Molecular medicine (Cambridge, Mass.)</journal><pubmed_title>2',3',4'-Trihydroxychalcone changes estrogen receptor α regulation of genes and breast cancer cell proliferation by a reprogramming mechanism.</pubmed_title><pmcid>PMC9036729</pmcid><funding_grant_id>1 R43 DK109862-01</funding_grant_id><funding_grant_id>1 R43 AG072965-01</funding_grant_id><funding_grant_id>R01 DK113019</funding_grant_id><funding_grant_id>R43 AG072965</funding_grant_id><funding_grant_id>R43 DK109862</funding_grant_id><funding_grant_id>DK113019-01A1</funding_grant_id><pubmed_authors>Yuan C</pubmed_authors><pubmed_authors>Chang A</pubmed_authors><pubmed_authors>Wang JC</pubmed_authors><pubmed_authors>Cohen I</pubmed_authors><pubmed_authors>Leitman DC</pubmed_authors><pubmed_authors>Herber CB</pubmed_authors></additional><is_claimable>false</is_claimable><name>2',3',4'-Trihydroxychalcone changes estrogen receptor α regulation of genes and breast cancer cell proliferation by a reprogramming mechanism.</name><description>&lt;h4>Background&lt;/h4>Menopausal hormone therapy (MHT) is recommended for only five years to treat vasomotor symptoms and vulvovaginal atrophy because of safety concerns with long-term treatment. We investigated the ability of 2',3',4'-trihydroxychalcone (2',3',4'-THC) to modulate estrogen receptor (ER)-mediated responses in order to find drug candidates that could potentially prevent the adverse effects of long-term MHT treatment.&lt;h4>Methods&lt;/h4>Transfection assays, real time-polymerase chain reaction, and microarrays were used to evaluate the effects of 2',3',4'-THC on gene regulation. Radioligand binding studies were used to determine if 2',3',4'-THC binds to ERα. Cell proliferation was examined in MCF-7 breast cancer cells by using growth curves and flow cytometry. Western blots were used</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-06-01T02:00:22.549Z</modification><creation>2024-10-17T20:04:52.74Z</creation></dates><accession>S-EPMC9036729</accession><cross_references><pubmed>35468719</pubmed><doi>10.1186/s10020-022-00470-z</doi></cross_references></HashMap>