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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1-s2.0-S2666979X25002368-main.pdf Bereitstellung unter der CC-Lizenz: Creative Commons Attribution. Download (10MB) |
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 Dasmeh, Pouria UNSPECIFIED UNSPECIFIED UNSPECIFIED Giel, Ann-Sophie UNSPECIFIED UNSPECIFIED UNSPECIFIED Franitza, Marek UNSPECIFIED UNSPECIFIED UNSPECIFIED Jonas, Christoph UNSPECIFIED UNSPECIFIED UNSPECIFIED Thieme, René UNSPECIFIED UNSPECIFIED UNSPECIFIED Heider, Dominik UNSPECIFIED UNSPECIFIED UNSPECIFIED Palles, Claire UNSPECIFIED UNSPECIFIED UNSPECIFIED Fitzgerald, Rebecca Claire UNSPECIFIED UNSPECIFIED UNSPECIFIED Gockel, Ines UNSPECIFIED UNSPECIFIED UNSPECIFIED Maj, Carlo UNSPECIFIED UNSPECIFIED UNSPECIFIED Schumacher, Johannes UNSPECIFIED 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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https://orcid.org/0009-0009-0322-2577