Wenzel, Marten C. ORCID: 0009-0009-0322-2577, Dasmeh, Pouria, Plum, Patrick S. ORCID: 0000-0002-8165-4553, Giel, Ann-Sophie, Hoppe, Sascha ORCID: 0000-0001-9246-3747, Franitza, Marek, Jonas, Christoph, Thieme, René, Zhao, Yue ORCID: 0000-0002-6790-3402, Heider, Dominik, Palles, Claire, Fitzgerald, Rebecca Claire, Bruns, Christiane J. ORCID: 0000-0001-6590-8181, Buettner, Reinhard ORCID: 0000-0001-8806-4786, Quaas, Alexander ORCID: 0000-0002-3537-6011, Gockel, Ines, Maj, Carlo, Chon, Seung-Hun ORCID: 0000-0002-8923-6428, Schumacher, Johannes and Hillmer, Axel M. ORCID: 0000-0002-3381-7266 (2025). Single-cell analysis of Barrett’s esophagus and carcinoma reveals cell types conferring risk via genetic predisposition. Cell Genomics, 5 (10). pp. 1-19. Elsevier. ISSN 2666-979X

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Identification Number:10.1016/j.xgen.2025.100980

Abstract

[Artikel-Nr.: 100980] Inherited genetic variants contribute to Barrett’s esophagus (BE) and esophageal adenocarcinoma (EAC), but it is unknown which cell types are involved in this process. We performed single-cell RNA sequencing of BE, EAC, and paired normal tissues and integrated genome-wide association data to determine cell-type-specific genetic risk and cellular processes that contribute to BE and EAC. The analysis reveals that EAC development is driven to a greater extent by local cellular processes than BE development and suggests that one cell type of BE origin (intestinal metaplasia cells) and cellular processes that control the differentiation of columnar cells are of particular relevance for EAC development. Specific subtypes of fibroblasts and endothelial cells likely contribute to BE and EAC development, while dendritic cells and CD4+ memory T cells seem to contribute to BE development. The diagnostic value of markers characterizing the cell types and cellular processes should be explored for EAC prediction.

Item Type: Article
Creators:
Creators
Email
ORCID
ORCID Put Code
Wenzel, Marten C.
UNSPECIFIED
UNSPECIFIED
Dasmeh, Pouria
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Plum, Patrick S.
UNSPECIFIED
UNSPECIFIED
Giel, Ann-Sophie
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Hoppe, Sascha
UNSPECIFIED
UNSPECIFIED
Franitza, Marek
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Jonas, Christoph
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Thieme, René
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Zhao, Yue
UNSPECIFIED
UNSPECIFIED
Heider, Dominik
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Palles, Claire
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Fitzgerald, Rebecca Claire
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Bruns, Christiane J.
UNSPECIFIED
UNSPECIFIED
Buettner, Reinhard
UNSPECIFIED
UNSPECIFIED
Quaas, Alexander
UNSPECIFIED
UNSPECIFIED
Gockel, Ines
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Maj, Carlo
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Chon, Seung-Hun
UNSPECIFIED
UNSPECIFIED
Schumacher, Johannes
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Hillmer, Axel M.
UNSPECIFIED
UNSPECIFIED
URN: urn:nbn:de:hbz:38-806630
Identification Number: 10.1016/j.xgen.2025.100980
Journal or Publication Title: Cell Genomics
Volume: 5
Number: 10
Page Range: pp. 1-19
Number of Pages: 19
Date: 8 October 2025
Publisher: Elsevier
ISSN: 2666-979X
Language: English
Faculty: Faculty of Medicine
Divisions: Faculty of Medicine > Chirurgie > Klinik und Poliklinik für Allgemein-, Viszeral-, Thorax- und Transplantationschirurgie
Faculty of Medicine > Pathologie und Neuropathologie > Institut für Pathologie
Zentrum für Molekulare Medizin
Subjects: Medical sciences Medicine
['eprint_fieldname_oa_funders' not defined]: Publikationsfonds UzK
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/80663

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