Evidence map›Paper›PMID 40847602›Full record

ArticleThe FEBS journal2026

CLEC18A interacts with sulfated glycosaminoglycans and controls clear cell renal cell carcinoma progression.

Gustav Jonsson, Maura Hofmann, Stefan Mereiter, Lauren Hartley-Tassell, Masahiro Onji, Irma Sakic, Tiago Oliveira, David Hoffmann, Maria Novatchkova, Alexander Schleiffer and 1 more

Abstract read
In one paragraph

Article in The FEBS journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Gustav JonssonInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.ORCID 0000-0001-6692-8395
Maura HofmannInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.
Stefan MereiterInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.
Lauren Hartley-TassellInstitute for Glycomics, Griffith University, Southport, Australia.
Masahiro OnjiInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.
Irma SakicInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.
Tiago OliveiraInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.
David HoffmannInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.
Maria NovatchkovaInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.
Alexander SchleifferInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.
Josef M PenningerInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, IMBA, Dr. Bohr-Gasse 3, Vienna, Austria.

Funding

Austrian Science Fund ESP 166Bundesministerium für Bildung und Forschung 01KX2324Canada Research Chairs F18-01336Fundació la Marató de TV3 202125-31H2020 Marie Skłodowska-Curie Actions 841319Österreichischen Akademie der Wissenschaften DOC fellowshipT. Von Zastrow Foundation
6 · The paper itself

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.

Indexed as

Carcinoma, Renal CellGlycosaminoglycansKidney NeoplasmsLectins, C-TypeAnimalsCell Line, TumorDisease ProgressionGene Expression Regulation, NeoplasticHumansMiceGlycosaminoglycansLectins, C-Typeclear cell renal cell carcinomaC‐type lectinglycosaminoglycanproteoglycanproximal tubule

Identifiers

PMID40847602
PMCPMC12871919

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.