<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pique-Gili M</submitter><funding>Alfonso Martín Escudero Foundation</funding><funding>NCATS NIH HHS</funding><funding>University Jaume I Department of Mathematics</funding><funding>Belgian American Educational Foundation Inc</funding><funding>Ramon Areces Foundation</funding><funding>National Institutes of Health</funding><funding>August Pi i Sunyer Institute of Biomedical Research</funding><funding>Cholangiocarcinoma Foundation</funding><funding>University of Barcelona</funding><funding>Spanish Association for the Study of the Liver</funding><funding>Horizon 2020 Framework Programme</funding><funding>Samuel Waxman Cancer Research Foundation</funding><funding>Ministerio de Ciencia e Innovación</funding><funding>National Institute for Health Research (NIHR)</funding><funding>NCI NIH HHS</funding><funding>Catalan Digestology Society</funding><funding>US Department of Defense</funding><funding>Damon Runyon Cancer Research Foundation</funding><funding>Spanish Association Against Cancer Scientific Foundation</funding><funding>NIH HHS</funding><funding>Icahn School of Medicine at Mount Sinai</funding><pagination>101212</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11550205</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(11)</volume><pubmed_abstract>&lt;h4>Background &amp; aims&lt;/h4>Transforming growth factor β (TGF-β) plays an oncogenic role in advanced cancer by promoting cell proliferation, metastasis and immunosuppression. &lt;i>PMEPA1&lt;/i> (prostate transmembrane protein androgen induced 1) has been shown to promote TGF-β oncogenic effects in other tumour types. Thus, we aimed to explore the role of &lt;i>PMEPA1&lt;/i> in hepatocellular carcinoma (HCC).&lt;h4>Methods&lt;/h4>We analysed 1,097 tumours from patients with HCC, including discovery (n = 228) and validation (n = 361) cohorts with genomic and clinicopathological data. &lt;i>PMEPA1&lt;/i> levels were assessed by qPCR (n = 228), gene expression data (n = 869) and at the single-cell level (n = 54). Genetically engineered mouse models overexpressing &lt;i>MYC+PMEPA1&lt;/i> compared to &lt;i>MYC&lt;/i> were generated</pubmed_abstract><journal>JHEP reports : innovation in hepatology</journal><pubmed_title>Oncogenic role of PMEPA1 and its association with immune exhaustion and TGF-β activation in HCC.</pubmed_title><pmcid>PMC11550205</pmcid><funding_grant_id>R01 CA285580</funding_grant_id><funding_grant_id>P30 CA196521</funding_grant_id><funding_grant_id>S10 OD030463</funding_grant_id><funding_grant_id>S10 OD026880</funding_grant_id><funding_grant_id>UL1 TR004419</funding_grant_id><funding_grant_id>R01 CA273932</funding_grant_id><pubmed_authors>Fernandez-Martinez E</pubmed_authors><pubmed_authors>Montironi C</pubmed_authors><pubmed_authors>Pique-Gili M</pubmed_authors><pubmed_authors>Barcena-Varela M</pubmed_authors><pubmed_authors>Peix J</pubmed_authors><pubmed_authors>Sia D</pubmed_authors><pubmed_authors>Pinyol R</pubmed_authors><pubmed_authors>Gris-Oliver A</pubmed_authors><pubmed_authors>Lindblad KE</pubmed_authors><pubmed_authors>Thung SN</pubmed_authors><pubmed_authors>Llovet JM</pubmed_authors><pubmed_authors>Mauro E</pubmed_authors><pubmed_authors>Mesropian A</pubmed_authors><pubmed_authors>Ruiz de Galarreta M</pubmed_authors><pubmed_authors>Cappuyns S</pubmed_authors><pubmed_authors>Lambrechts D</pubmed_authors><pubmed_authors>Esteban-Fabro R</pubmed_authors><pubmed_authors>Keraite I</pubmed_authors><pubmed_authors>Andreu-Oller C</pubmed_authors><pubmed_authors>Abril-Fornaguera J</pubmed_authors><pubmed_authors>Dekervel J</pubmed_authors><pubmed_authors>Martinez-Quetglas I</pubmed_authors><pubmed_authors>Torres-Martin M</pubmed_authors><pubmed_authors>Lujambio A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Oncogenic role of PMEPA1 and its association with immune exhaustion and TGF-β activation in HCC.</name><description>&lt;h4>Background &amp; aims&lt;/h4>Transforming growth factor β (TGF-β) plays an oncogenic role in advanced cancer by promoting cell proliferation, metastasis and immunosuppression. &lt;i>PMEPA1&lt;/i> (prostate transmembrane protein androgen induced 1) has been shown to promote TGF-β oncogenic effects in other tumour types. Thus, we aimed to explore the role of &lt;i>PMEPA1&lt;/i> in hepatocellular carcinoma (HCC).&lt;h4>Methods&lt;/h4>We analysed 1,097 tumours from patients with HCC, including discovery (n = 228) and validation (n = 361) cohorts with genomic and clinicopathological data. &lt;i>PMEPA1&lt;/i> levels were assessed by qPCR (n = 228), gene expression data (n = 869) and at the single-cell level (n = 54). Genetically engineered mouse models overexpressing &lt;i>MYC+PMEPA1&lt;/i> compared to &lt;i>MYC&lt;/i> were generated</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-06-02T10:38:37.21Z</modification><creation>2025-04-04T00:21:55.866Z</creation></dates><accession>S-EPMC11550205</accession><cross_references><pubmed>39524206</pubmed><doi>10.1016/j.jhepr.2024.101212</doi></cross_references></HashMap>