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1000 Titel
  • Loss of CDX2 in colorectal cancer is associated with histopathologic subtypes and microsatellite instability but is prognostically inferior to hematoxylin–eosin-based morphologic parameters from the WHO classification
1000 Autor/in
  1. Konukiewitz, Björn |
  2. Schmitt, Maxime |
  3. Silva, Miguel |
  4. Pohl, Junika |
  5. Lang, Corinna |
  6. Steiger, Katja |
  7. Halfter, Kathrin |
  8. Engel, Jutta |
  9. Schlitter, Anna Melissa |
  10. Boxberg, Melanie |
  11. Pfarr, Nicole |
  12. Wilhelm, Dirk |
  13. Foersch, Sebastian |
  14. Tschurtschenthaler, Markus |
  15. Weichert, Wilko |
  16. Jesinghaus, Moritz |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-10-06
1000 Erschienen in
1000 Quellenangabe
  • 125(12):1632-1646
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1038/s41416-021-01553-0 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651779/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Immunohistochemical loss of CDX2 has been proposed as a biomarker of dismal survival in colorectal carcinoma (CRC), especially in UICC Stage II/III. However, it remains unclear, how CDX2 expression is related to central hematoxylin-eosin (HE)-based morphologic parameters defined by 2019 WHO classification and how its prognostic relevance is compared to these parameters.!##!Methods!#!We evaluated CDX2 expression in 1003 CRCs and explored its prognostic relevance compared to CRC subtypes, tumour budding and WHO grade in the overall cohort and in specific subgroups.!##!Results!#!CDX2-low/absent CRCs were enriched in specific morphologic subtypes, right-sided and microsatellite-instable (MSI-H) CRCs (P < 0.001) and showed worse survival characteristics in the overall cohort/UICC Stage II/III (e.g. DFS: P = 0.005) and in microsatellite stable and left-sided CRCs, but not in MSI-H or right-sided CRCs. Compared with CDX2, all HE-based markers showed a significantly better prognostic discrimination in all scenarios. In multivariate analyses including all morphologic parameters, CDX2 was not an independent prognostic factor.!##!Conclusion!#!CDX2 loss has some prognostic impact in univariate analyses, but its prognostic relevance is considerably lower compared to central HE-based morphologic parameters defined by the WHO classification and vanishes in multivariate analyses incorporating these factors.
1000 Sacherschließung
lokal Biomarkers
lokal Female [MeSH]
lokal Prognostic markers
lokal Humans [MeSH]
lokal Hematoxylin/metabolism [MeSH]
lokal World Health Organization [MeSH]
lokal Eosine Yellowish-(YS)/metabolism [MeSH]
lokal Microsatellite Instability [MeSH]
lokal CDX2 Transcription Factor/metabolism [MeSH]
lokal Article
lokal Male [MeSH]
lokal Prognosis [MeSH]
lokal Colorectal Neoplasms/genetics [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/S29udWtpZXdpdHosIEJqw7Zybg==|https://frl.publisso.de/adhoc/uri/U2NobWl0dCwgTWF4aW1l|https://frl.publisso.de/adhoc/uri/U2lsdmEsIE1pZ3VlbA==|https://frl.publisso.de/adhoc/uri/UG9obCwgSnVuaWth|https://frl.publisso.de/adhoc/uri/TGFuZywgQ29yaW5uYQ==|https://orcid.org/0000-0002-7269-5433|https://frl.publisso.de/adhoc/uri/SGFsZnRlciwgS2F0aHJpbg==|https://frl.publisso.de/adhoc/uri/RW5nZWwsIEp1dHRh|https://frl.publisso.de/adhoc/uri/U2NobGl0dGVyLCBBbm5hIE1lbGlzc2E=|https://frl.publisso.de/adhoc/uri/Qm94YmVyZywgTWVsYW5pZQ==|https://orcid.org/0000-0002-5977-5375|https://frl.publisso.de/adhoc/uri/V2lsaGVsbSwgRGlyaw==|https://frl.publisso.de/adhoc/uri/Rm9lcnNjaCwgU2ViYXN0aWFu|https://orcid.org/0000-0002-0060-4790|https://frl.publisso.de/adhoc/uri/V2VpY2hlcnQsIFdpbGtv|https://orcid.org/0000-0002-0018-5661
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1000 Erstellt am 2023-04-26T16:01:04.741+0200
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