Wang, Jing; Koch, Dominik ORCID: 0000-0002-7409-0032; Hofmann, Felix Oliver
ORCID: 0000-0002-6913-2429; Härtwig, Daniel; Beirith, Iris
ORCID: 0009-0002-6129-3524; Janssen, Klaus-Peter; Bazhin, Alexandr V.; Niess, Hanno; Werner, Jens; Renz, Bernhard
ORCID: 0000-0001-9574-8051; Ilmer, Matthias
ORCID: 0000-0001-9597-1368
(2023):
WNT enhancing signals in pancreatic cancer are transmitted by LGR6.
Aging.
ISSN 1945-4589
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Abstract
The G-protein-coupled receptor LGR6 associates with ligands of the R-Spondin (RSPO) family to potentiate preexisting signals of the canonical WNT pathway. However, its importance in pancreatic ductal adenocarcinoma (PDAC) remains unclear. Here, we show that LGR6 is differentially expressed in various PDAC cell lines of mesenchymal and epithelial phenotype, respectively, siding with the latter subsets. LGR6 expression is altered based upon the cells’ WNT activation status. Furthermore, extrinsic enhancement of WNT pathway signaling increased LGR6 expression suggestive of a reinforcing self-regulatory loop in highly WNT susceptible cells. Downregulation of LGR6 on the other hand, seemed to tamper those effects. Last, downregulation of LGR6 reduced cancer stemness as determined by functional in vitro assays. These findings shed new insights into regulatory mechanisms for the canonical WNT pathway in pancreatic cancer cells. It may also have potential value for treatment stratification of PDAC.
Doc-Type: | Article (LMU Hospital) |
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Organisational unit (Faculties): | 07 Medicine > Medical Center of the University of Munich > Clinic for General, Visceral, Vascular and Transplant Surgery |
DFG subject classification of scientific disciplines: | Life sciences |
Date Deposited: | 14. Nov 2023 10:03 |
Last Modified: | 07. Dec 2023 12:19 |
URI: | https://oa-fund.ub.uni-muenchen.de/id/eprint/899 |
DFG: | Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - 491502892 |