<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hsiao JJ</submitter><funding>University of Iowa Start up funds</funding><funding>U.S. Department of Defense</funding><pagination>22208</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8592995</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>Supraphysiologic androgen (SPA) inhibits cell proliferation in prostate cancer (PCa) cells by transcriptional repression of DNA replication and cell-cycle genes. In this study, quantitative glycoprotein profiling identified androgen-regulated glycoprotein networks associated with SPA-mediated inhibition of PCa cell proliferation, and androgen-regulated glycoproteins in clinical prostate tissues. SPA-regulated glycoprotein networks were enriched for translation factors and ribosomal proteins, proteins that are known to be O-GlcNAcylated in response to various cellular stresses. Thus, androgen-regulated glycoproteins are likely to be targeted for O-GlcNAcylation. Comparative analysis of glycosylated proteins in PCa cells and clinical prostate tissue identified androgen-regulated glycoprotein</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Discovery proteomics defines androgen-regulated glycoprotein networks in prostate cancer cells, as well as putative biomarkers of prostatic diseases.</pubmed_title><pmcid>PMC8592995</pmcid><funding_grant_id>W81XWH-08-1-0471</funding_grant_id><pubmed_authors>Hsiao JJ</pubmed_authors><pubmed_authors>Wright ME</pubmed_authors><pubmed_authors>Ng BH</pubmed_authors><pubmed_authors>Lee J</pubmed_authors><pubmed_authors>Smits MM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Discovery proteomics defines androgen-regulated glycoprotein networks in prostate cancer cells, as well as putative biomarkers of prostatic diseases.</name><description>Supraphysiologic androgen (SPA) inhibits cell proliferation in prostate cancer (PCa) cells by transcriptional repression of DNA replication and cell-cycle genes. In this study, quantitative glycoprotein profiling identified androgen-regulated glycoprotein networks associated with SPA-mediated inhibition of PCa cell proliferation, and androgen-regulated glycoproteins in clinical prostate tissues. SPA-regulated glycoprotein networks were enriched for translation factors and ribosomal proteins, proteins that are known to be O-GlcNAcylated in response to various cellular stresses. Thus, androgen-regulated glycoproteins are likely to be targeted for O-GlcNAcylation. Comparative analysis of glycosylated proteins in PCa cells and clinical prostate tissue identified androgen-regulated glycoprotein</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2026-05-08T03:24:48.885Z</modification><creation>2025-05-29T20:26:09.328Z</creation></dates><accession>S-EPMC8592995</accession><cross_references><pubmed>34782677</pubmed><doi>10.1038/s41598-021-01554-2</doi></cross_references></HashMap>