<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-13T11:26:09Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10256/16145" metadataPrefix="mets">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10256/16145</identifier><datestamp>2024-06-18T12:40:26Z</datestamp><setSpec>com_2072_452955</setSpec><setSpec>com_2072_2054</setSpec><setSpec>col_2072_453079</setSpec></header><metadata><mets xmlns="http://www.loc.gov/METS/" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_10256-16145" TYPE="DSpace ITEM" PROFILE="DSpace METS SIP Profile 1.0" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd" OBJID="&#xa;&#x9;&#x9;&#x9;&#x9;hdl:10256/16145">
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                  <mods:namePart>Corominas Faja, Bruna</mods:namePart>
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                  <mods:namePart>Cuyàs, Elisabet</mods:namePart>
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                  <mods:namePart>Gumuzio, Juan</mods:namePart>
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                  <mods:namePart>Bosch Barrera, Joaquim</mods:namePart>
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                  <mods:namePart>Leis, Olatz</mods:namePart>
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                  <mods:namePart>Martin, Ángel G.</mods:namePart>
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                  <mods:namePart>Menéndez Menéndez, Javier Abel</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-06-18T12:40:26Z</mods:dateAccessioned>
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               <mods:identifier type="uri">http://hdl.handle.net/10256/16145</mods:identifier>
               <mods:abstract>Cancer stem cells (CSC) may take advantage of the Warburg effect-induced siphoning of metabolic intermediates into de novo fatty acid biosynthesis to increase self-renewal growth. We examined the anti-CSC effects of the antifungal polyketide soraphen A, a specific inhibitor of the first committed step of lipid biosynthesis catalyzed by acetyl-CoA carboxylase (ACACA). The mammosphere formation capability of MCF-7 cells was reduced following treatment with soraphen A in a dose-dependent manner. MCF-7 cells engineered to overexpress the oncogene HER2 (MCF-7/HER2 cells) were 5-fold more sensitive than MCF-7 parental cells to soraphen A-induced reductions in mammosphere-forming efficiency. Soraphen A treatment notably decreased aldehyde dehydrogenase (ALDH)-positive CSC-like cells and impeded the HER2’s ability to increase the ALDH+-stem cell population. The following results confirmed that soraphen A-induced suppression of CSC populations occurred throughACACA-driven lipogenesis: a.) exogenous supplementation with supraphysiological concentrations of oleic acid fully rescued mammosphere formation in the presence of soraphen A and b.) mammosphere cultures of MCF-7 cells with stably silenced expression of the cytosolic isoform ACACA1, which specifically participates in de novo lipogenesis, were mostly refractory to soraphen A treatment. Our findings reveal for the first time that ACACA may constitute a previously unrecognized target for novel anti-breast CSC therapies</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">Reconeixement 3.0 Espanya http://creativecommons.org/licenses/by/3.0/es/deed.ca info:eu-repo/semantics/openAccess</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Mama -- Càncer</mods:topic>
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               <mods:subject>
                  <mods:topic>Breast -- Cancer</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Cèl·lules mare -- Càncer</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Stem cells -- Cancer</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Chemical inhibition of acetyl-CoA carboxylase suppresses self-renewal growth of cancer stem cells</mods:title>
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               <mods:genre>info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion peer-reviewed</mods:genre>
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