<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Gadad SS</submitter><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pubmed_abstract>Recent studies have demonstrated that a subset of long "noncoding" RNAs (lncRNAs) produce functional polypeptides and proteins. In this study, we discovered a 132 amino acid protein in human breast cancer cells named XCP (X-linked Cancer-associated Polypeptide), which is encoded by &lt;i>lncRNA1456&lt;/i> (a.k.a. &lt;i>RHOXF1P3&lt;/i>), a transcript previously thought to be noncoding. &lt;i>lncRNA1456&lt;/i> is a pancreas- and testis-specific RNA whose gene is located on chromosome X. We found that the expression of &lt;i>lncRNA1456&lt;/i> and XCP are highly upregulated in the luminal A, luminal B, and HER2 molecular subtypes of breast cancer. XCP modulates both estrogen-dependent and estrogen-independent growth of breast cancer cells by regulating cancer pathways, as shown in cell and xenograft models. XCP shares some homology with homeodomain-containing proteins and interacts with the histone demethylase plant homeodomain finger protein 8 (PHF8), which is also encoded by an X-linked gene. Mechanistically, XCP stimulates the histone demethylase activity of PHF8 to regulate gene expression in breast cancer cells. These findings identify XCP as a coregulator of transcription and emphasize the need to interrogate the potential functional roles of open reading frames originating from noncoding RNAs.</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2025.03.21.644649</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11974697</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>X-Linked Cancer-Associated Polypeptide (XCP) from &amp;lt;i&amp;gt;lncRNA1456&amp;lt;/i&amp;gt; Cooperates with PHF8 to Regulate Gene Expression and Cellular Pathways in Breast Cancer.</pubmed_title><pmcid>PMC11974697</pmcid><funding_grant_id>S10 OD021684</funding_grant_id><funding_grant_id>R16 GM149497</funding_grant_id><funding_grant_id>P30 CA142543</funding_grant_id><pubmed_authors>Koul S</pubmed_authors><pubmed_authors>Peng Y</pubmed_authors><pubmed_authors>Nagari A</pubmed_authors><pubmed_authors>Thornton M</pubmed_authors><pubmed_authors>Camacho CV</pubmed_authors><pubmed_authors>Malladi VS</pubmed_authors><pubmed_authors>Kraus WL</pubmed_authors><pubmed_authors>Sundaresan A</pubmed_authors><pubmed_authors>Nandu T</pubmed_authors><pubmed_authors>Gadad SS</pubmed_authors><pubmed_authors>Gong X</pubmed_authors></additional><is_claimable>false</is_claimable><name>X-Linked Cancer-Associated Polypeptide (XCP) from &amp;lt;i&amp;gt;lncRNA1456&amp;lt;/i&amp;gt; Cooperates with PHF8 to Regulate Gene Expression and Cellular Pathways in Breast Cancer.</name><description>Recent studies have demonstrated that a subset of long "noncoding" RNAs (lncRNAs) produce functional polypeptides and proteins. In this study, we discovered a 132 amino acid protein in human breast cancer cells named XCP (X-linked Cancer-associated Polypeptide), which is encoded by &lt;i>lncRNA1456&lt;/i> (a.k.a. &lt;i>RHOXF1P3&lt;/i>), a transcript previously thought to be noncoding. &lt;i>lncRNA1456&lt;/i> is a pancreas- and testis-specific RNA whose gene is located on chromosome X. We found that the expression of &lt;i>lncRNA1456&lt;/i> and XCP are highly upregulated in the luminal A, luminal B, and HER2 molecular subtypes of breast cancer. XCP modulates both estrogen-dependent and estrogen-independent growth of breast cancer cells by regulating cancer pathways, as shown in cell and xenograft models. XCP shares some homology with homeodomain-containing proteins and interacts with the histone demethylase plant homeodomain finger protein 8 (PHF8), which is also encoded by an X-linked gene. Mechanistically, XCP stimulates the histone demethylase activity of PHF8 to regulate gene expression in breast cancer cells. These findings identify XCP as a coregulator of transcription and emphasize the need to interrogate the potential functional roles of open reading frames originating from noncoding RNAs.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-04-08T19:27:39.155Z</modification><creation>2026-04-08T13:31:15.959Z</creation></dates><accession>S-EPMC11974697</accession><cross_references><pubmed>40196671</pubmed><doi>10.1101/2025.03.21.644649</doi></cross_references></HashMap>