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CLEC18A interacts with sulfated glycosaminoglycans and controls clear cell renal cell carcinoma progression
Open accessPublished version of a preprint
Abstract
C‐type lectins are a large protein family with essential functions in both health and disease. In cancer, some C‐type lectins have been found to both promote and inhibit tumor growth, but many of the C‐type lectins still remain uncharacterized. Here, we report a key role of the C‐type lectin domain family 18 members (CLEC18 family) in the progression of clear cell renal cell carcinoma (ccRCC). The CLEC18 family is conserved across the entire Chordata phylum, with a high frequency of duplication events in humans compared to other species. We found that CLEC18A is exclusively expressed in the proximal tubule of the kidney and the medial habenula of the brain. We further identified sulfated glycosaminoglycans as the main CLEC18A ligand, making them unique among C‐type lectins. In ccRCC patients, high expression of genes in the CLEC18 family in the tumor is associated with improved survival. In mouse models of ccRCC, deletion of the mouse ortholog, Clec18a , resulted in enhanced tumor growth. Our results establish CLEC18A as a newly identified and critical regulator of ccRCC tumor growth and highlight the potential benefit of modulating expression of CLEC18 family genes in the renal tumor microenvironment.
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Metadata
- Authors
- Jonsson, G., Hofmann, M., Mereiter, S., Hartley‐Tassell, L., Onji, M., Sakic, I., Oliveira, T., Hoffmann, D., Novatchkova, M., Schleiffer, A., & Penninger, J. M.
- Affiliations
- Institute of Molecular Biotechnology (AT)
- Griffith University (AU)
- Corresponding author
- Jonsson, Gustav
- Penninger, Josef M.
- ORCID
- Venue
- The FEBS Journal
- Publisher
- Wiley
- Published
- 2025-08-23
- Volume
- 293
- Issue
- 3
- Pages
- 709-728
- ISSN
- 1742-464X (ISSN-L)
- 1742-4658
- PMC
- PMC12871919
- OpenAlex
- W4413471203
- Cited by
- 1
- References
- 4
- Citations by year
- 2025: 1
- FWCI
- 0.65
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- FEBS Journal (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Bundesministerium für Bildung und Forschung (01KX2324)
- Österreichische Akademie der Wissenschaften
- T. Von Zastrow Foundation
- Austrian Science Fund (ESP 166)
- Fundació la Marató de TV3 (202125‐31)
- H2020 Marie Skłodowska-Curie Actions (841319)
- Canada Research Chairs (F18‐01336)
- Topics
- Health Sciences › Medicine › Oncology › Renal cell carcinoma treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
- Life Sciences › Immunology and Microbiology › Immunology › Galectins and Cancer Biology
- Keywords
- C-type lectin, clear cell renal cell carcinoma, sulfated glycosaminoglycans, tumor progression, tumor microenvironment, proximal tubule, medial habenula, gene duplication, tumor growth, patient survival
- MeSH terms
- Animals, Carcinoma, Renal Cell, Glycosaminoglycans, Humans, Kidney Neoplasms, Gene Expression Regulation, Neoplastic, Disease Progression, Lectins, C-Type, Cell Line, Tumor, Mice
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