
<ns0:uwmetadata xmlns:ns0="http://phaidra.univie.ac.at/XML/metadata/V1.0" xmlns:ns1="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0" xmlns:ns10="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0" xmlns:ns11="http://phaidra.univie.ac.at/XML/metadata/provenience/V1.0/entity" xmlns:ns12="http://phaidra.univie.ac.at/XML/metadata/digitalbook/V1.0" xmlns:ns13="http://phaidra.univie.ac.at/XML/metadata/etheses/V1.0" xmlns:ns2="http://phaidra.univie.ac.at/XML/metadata/extended/V1.0" xmlns:ns3="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/entity" xmlns:ns4="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/requirement" xmlns:ns5="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/educational" xmlns:ns6="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/annotation" xmlns:ns7="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/classification" xmlns:ns8="http://phaidra.univie.ac.at/XML/metadata/lom/V1.0/organization" xmlns:ns9="http://phaidra.univie.ac.at/XML/metadata/histkult/V1.0">
  <ns1:general>
    <ns1:identifier>o:3499</ns1:identifier>
    <ns1:title language="en">Screening for oncogenic AF1q expression predicts disease recurrence in gastric cancer patients</ns1:title>
    <ns1:language>en</ns1:language>
    <ns1:description language="en">AF1q associates with tumor progression and metastases upon WNT signaling. The downstream WNT target CD44 has demonstrated prognostic significance in gastric cancer (GC). This study evaluates the impact of AF1q on tumor stage and survival in GC patients. Immunohistochemical marker expression was analyzed and data were processed to correlation and survival analysis. Out of 182 GC samples, 178 (97.8%) showed moderate to high AF1q expression (pâ&lt;â0.001), these samples correlated with positive lymph node stage (pâ=â0.036). In a subgroup analysis of patients with nodal-positive GC (nâ=â129, 70.9%), enhanced tumoral AF1q expression resulted in impaired recurrence-free survival (RFS, pâ=â0.030). Enhanced tumoral CD44 expression resulted in impaired disease-specific survival (DSS) in the subgroup of patients with nodal-positive GC (pâ=â0.031) as well as in the overall GC group (pâ=â0.005). AF1q demonstrated as an independent prognostic marker for RFS (pâ=â0.035) and CD44 for DSS (pâ=â0.036). AF1q has shown potential for prognostication of RFS in GC patients and is predominantly expressed in nodal-positive GC. Testing AF1q provides a possibility of identifying patients with locoregional (and advanced) disease, particularly at risk for disease recurrence. Implementing AF1q into the diagnostic process may facilitate screening, prognosis estimation as well as consideration of preoperative multimodal treatment in patients qualifying for elective upfront surgery.</ns1:description>
    <ns1:keyword language="en">AF1q; CD44; Lymph node stage; Recurrence; Survival; Gastric cancer</ns1:keyword>
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      <ns2:resource>1552099</ns2:resource>
      <ns2:identifier>10.1038/s41598-024-67058-x</ns2:identifier>
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    <ns1:upload_date>2024-09-09T07:00:21.519Z</ns1:upload_date>
    <ns1:status>44</ns1:status>
    <ns2:peer_reviewed>yes</ns2:peer_reviewed>
    <ns1:contribute seq="0">
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      <ns1:entity seq="0">
        <ns3:firstname>Elisabeth S.</ns3:firstname>
        <ns3:lastname>Gruber</ns3:lastname>
        <ns3:institution>Medical University of Vienna</ns3:institution>
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      <ns1:entity seq="5">
        <ns3:firstname>Georg</ns3:firstname>
        <ns3:lastname>Oberhuber</ns3:lastname>
        <ns3:institution>Medical University of Vienna / PIZ - patho im zentrum GmbH</ns3:institution>
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      <ns1:entity seq="7">
        <ns3:firstname>Michaela</ns3:firstname>
        <ns3:lastname>Schlederer</ns3:lastname>
        <ns3:institution>Medical University of Vienna</ns3:institution>
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      <ns1:entity seq="4">
        <ns3:firstname>Peter</ns3:firstname>
        <ns3:lastname>Birner</ns3:lastname>
        <ns3:institution>Medical University of Vienna</ns3:institution>
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        <ns3:firstname>Gerd</ns3:firstname>
        <ns3:lastname>Jomrich</ns3:lastname>
        <ns3:institution>Medical University of Vienna</ns3:institution>
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      <ns1:entity seq="6">
        <ns3:firstname>Sebastian F.</ns3:firstname>
        <ns3:lastname>Schoppmann</ns3:lastname>
        <ns3:institution>Medical University of Vienna</ns3:institution>
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      <ns1:entity seq="2">
        <ns3:firstname>William</ns3:firstname>
        <ns3:lastname>Tse</ns3:lastname>
        <ns3:institution>Case Western Reserve University</ns3:institution>
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        <ns3:firstname>Lukas</ns3:firstname>
        <ns3:lastname>Kenner</ns3:lastname>
        <ns3:institution>University of Veterinary Medicine Vienna / Medical University of Vienna / Center For Biomarker Research In Medicine</ns3:institution>
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        <ns3:orcid>0000-0003-2184-1338</ns3:orcid>
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  <ns12:digitalbook>
    <ns12:name_magazine language="en">Scientific Reports</ns12:name_magazine>
    <ns12:pagination>8</ns12:pagination>
    <ns12:volume>14</ns12:volume>
    <ns12:booklet>1</ns12:booklet>
    <ns12:publisher>Nature</ns12:publisher>
    <ns12:releaseyear>2024</ns12:releaseyear>
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