<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Peinetti N</submitter><funding>BLRD VA</funding><pagination>e165357</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9711867</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>132(23)</volume><pubmed_abstract>Androgen deprivation therapy (ADT) is the longstanding treatment for advanced prostate cancer (PC) because androgen receptor (AR) is the key therapeutic vulnerability for this disease. Bipolar androgen therapy (BAT) - the rapid cycling of supraphysiologic androgen (SPA) and low serum testosterone levels - is an alternative concept, but not all patients respond and acquired resistance can occur. In this issue of the JCI, Sena et al. developed a gene signature indicative of high AR activity to predict patient response to BAT, including a decline in both serum prostate-specific antigen (PSA) and tumor volume. Preclinical models showed that AR-mediated suppression of MYC, known to drive PC, was associated with decreased cell growth following SPA treatment. Because BAT eventually leads to resis</pubmed_abstract><journal>The Journal of clinical investigation</journal><pubmed_title>Is androgen receptor activity in metastatic prostate cancer a good biomarker for bipolar androgen therapy?</pubmed_title><pmcid>PMC9711867</pmcid><funding_grant_id>I01 BX002773</funding_grant_id><funding_grant_id>I01 BX005466</funding_grant_id><pubmed_authors>Peinetti N</pubmed_authors><pubmed_authors>Bilusic M</pubmed_authors><pubmed_authors>Burnstein KL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Is androgen receptor activity in metastatic prostate cancer a good biomarker for bipolar androgen therapy?</name><description>Androgen deprivation therapy (ADT) is the longstanding treatment for advanced prostate cancer (PC) because androgen receptor (AR) is the key therapeutic vulnerability for this disease. Bipolar androgen therapy (BAT) - the rapid cycling of supraphysiologic androgen (SPA) and low serum testosterone levels - is an alternative concept, but not all patients respond and acquired resistance can occur. In this issue of the JCI, Sena et al. developed a gene signature indicative of high AR activity to predict patient response to BAT, including a decline in both serum prostate-specific antigen (PSA) and tumor volume. Preclinical models showed that AR-mediated suppression of MYC, known to drive PC, was associated with decreased cell growth following SPA treatment. Because BAT eventually leads to resis</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-04T21:00:44.813Z</modification><creation>2025-02-18T23:35:00.158Z</creation></dates><accession>S-EPMC9711867</accession><cross_references><pubmed>36453547</pubmed><doi>10.1172/JCI165357</doi></cross_references></HashMap>