<?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>2026-07-21T14:20:14Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/9136" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/9136</identifier><datestamp>2025-06-13T10:44:27Z</datestamp><setSpec>com_20.500.12105_2173</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>com_20.500.12105_2052</setSpec><setSpec>col_20.500.12105_19597</setSpec><setSpec>col_20.500.12105_19616</setSpec><setSpec>col_20.500.12105_25179</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Abarrategi, Ander</subfield>
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      <subfield code="a">Gambera, Stefano</subfield>
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      <subfield code="a">Alfranca, Arantzazu</subfield>
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      <subfield code="a">Rodriguez-Milla, Miguel A</subfield>
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      <subfield code="a">Perez-Tavarez, Raquel</subfield>
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      <subfield code="a">Rouault-Pierre, Kevin</subfield>
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      <subfield code="a">Chakravarty, Probir</subfield>
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      <subfield code="a">Mulero, Francisca</subfield>
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      <subfield code="a">Trigueros, César</subfield>
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      <subfield code="a">Navarro, Samuel</subfield>
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      <subfield code="a">Bonnet, Dominique</subfield>
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      <subfield code="a">Garcia-Castro, Javier</subfield>
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      <subfield code="a">Mesenchymal progenitor cells (MPCs) have been hypothesized as cells of origin for sarcomas, and c-Fos transcription factor has been showed to act as an oncogene in bone tumors. In this study, we show c-Fos is present in most sarcomas with chondral phenotype, while multiple other genes are related to c-Fos expression pattern. To further define the role of c-Fos in sarcomagenesis, we expressed it in primary human MPCs (hMPCs), immortalized hMPCs and transformed murine MPCs (mMPCs). In immortalized hMPCs, c-Fos expression generated morphological changes, reduced mobility capacity and impaired adipogenic- and osteogenic-differentiation potentials. Remarkably, immortalized hMPCs or mMPCs expressing c-Fos generated tumors harboring a chondrogenic phenotype and morphology. Thus, here we show that c-Fos protein has a key role in sarcomas and that c-Fos expression in immortalized MPCs yields cell transformation and chondrogenic tumor formation.</subfield>
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      <subfield code="a">Sci Rep. 2018 Oct 23;8(1):15615.</subfield>
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      <subfield code="a">10.1038/s41598-018-33689-0</subfield>
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      <subfield code="a">30353072</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/9136</subfield>
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      <subfield code="a">c-Fos induces chondrogenic tumor formation in immortalized human mesenchymal progenitor cells</subfield>
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