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1000 Titel
  • The tight junction protein claudin 6 is a potential target for patient-individualized treatment in esophageal and gastric adenocarcinoma and is associated with poor prognosis
1000 Autor/in
  1. Simon, Adrian Georg |
  2. Lyu, Su Ir |
  3. Laible, Mark |
  4. Wöll, Stefan |
  5. Türeci, Özlem |
  6. Şahin, Uğur |
  7. Alakus, Hakan |
  8. Fahrig, Luca |
  9. Zander, Thomas |
  10. Buettner, Reinhard |
  11. Bruns, Christiane Josephine |
  12. Schroeder, Wolfgang |
  13. Gebauer, Florian |
  14. Quaas, Alexander |
1000 Verlag
  • BioMed Central
1000 Erscheinungsjahr 2023
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2023-08-17
1000 Erschienen in
1000 Quellenangabe
  • 21(1):552
1000 Copyrightjahr
  • 2023
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12967-023-04433-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436499/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>The prognosis of esophageal adenocarcinoma (EAC) and gastric adenocarcinoma (GAC) remains poor, and new therapeutic approaches are urgently needed. Claudin 6 (CLDN6) is an oncofetal antigen that is largely absent in healthy tissues and upregulated in several cancers, making it a promising therapeutical target. In this study, the expression of CLDN6 was assessed in an large Caucasian EAC and GAC cohort.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>RNA-Seq data from 89 EACs and 371 GACs were obtained from The Cancer Genome Atlas project and EAC/GAC cases were stratified by CLDN6 mRNA expression based on a survival-associated cutoff. For groups with CLDN6 expression above or below this cutoff, differential gene expression analyses were performed using DESeq, and dysregulated biological pathways were identified using the Enrichr tool. Additionally, CLDN6 protein expression was assessed in more than 800 EACs and almost 600 GACs using a CLDN6-specific immunohistochemical antibody (clone 58-4B-2) that is currently used in Phase I/II trials to identify patients with CLDN6-positive tumors (NCT05262530; NCT04503278). The expression of CLDN6 was also correlated with histopathological parameters and overall survival (OS).</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>EACs and GACs with high CLDN6 mRNA levels displayed an overexpression of pathways regulating the cell cycle, DNA replication, and receptor / extracellular matrix interactions. CLDN6 protein expression was associated with shorter OS in EAC and GAC, both in treatment-naïve subgroups and cohorts receiving neoadjuvant therapy. In multivariate analysis, CLDN6 protein expression was an independent adverse prognostic factor in EAC associated with a shorter OS (HR: 1.75; p = 0.01) and GAC (HR: 2.74; p = 0.028).</jats:p> </jats:sec><jats:sec> <jats:title>Conclusions</jats:title> <jats:p>High expression of CLDN6 mRNA is associated with the dysregulation of distinct biological pathways regulating cell growth, proliferation, and cell–matrix interactions. Clinically, the expression of CLDN6 protein is a valuable adverse prognostic marker in EAC and GAC.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Gastric cancer
lokal Stomach Neoplasms/genetics [MeSH]
lokal Humans [MeSH]
lokal CLDN6
lokal CAR T-cell therapy
lokal Tight Junction Proteins [MeSH]
lokal Aminocaproic Acid [MeSH]
lokal Medical and Health Sciences
lokal Adenocarcinoma
lokal Research
lokal Esophageal cancer
lokal Immunotherapy
lokal Adenocarcinoma/genetics [MeSH]
lokal Combination strategies
lokal Claudins/genetics [MeSH]
lokal Claudin
lokal Tight junctions
lokal Antibodies [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-2709-863X|https://frl.publisso.de/adhoc/uri/THl1LCBTdSBJcg==|https://frl.publisso.de/adhoc/uri/TGFpYmxlLCBNYXJr|https://frl.publisso.de/adhoc/uri/V8O2bGwsIFN0ZWZhbg==|https://frl.publisso.de/adhoc/uri/VMO8cmVjaSwgw5Z6bGVt|https://frl.publisso.de/adhoc/uri/xZ5haGluLCBVxJ91cg==|https://frl.publisso.de/adhoc/uri/QWxha3VzLCBIYWthbg==|https://frl.publisso.de/adhoc/uri/RmFocmlnLCBMdWNh|https://frl.publisso.de/adhoc/uri/WmFuZGVyLCBUaG9tYXM=|https://frl.publisso.de/adhoc/uri/QnVldHRuZXIsIFJlaW5oYXJk|https://frl.publisso.de/adhoc/uri/QnJ1bnMsIENocmlzdGlhbmUgSm9zZXBoaW5l|https://frl.publisso.de/adhoc/uri/U2Nocm9lZGVyLCBXb2xmZ2FuZw==|https://frl.publisso.de/adhoc/uri/R2ViYXVlciwgRmxvcmlhbg==|https://frl.publisso.de/adhoc/uri/UXVhYXMsIEFsZXhhbmRlcg==
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    1000 Förderer Universitätsklinikum Köln |
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