Evidence map›Paper›PMID 36478037›Full record

ArticleCancer immunology research2023

Extracellular Galectin 4 Drives Immune Evasion and Promotes T-cell Apoptosis in Pancreatic Cancer.

Tommy Lidström, Joshua Cumming, Rahul Gaur, Lars Frängsmyr, Ioannis S Pateras, Matthias J Mickert, Oskar Franklin, Mattias N E Forsell, Niklas Arnberg, Mitesh Dongre and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

35 citing papers in PubMed, 42 citations in OpenAlex.

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  11. HERV-K TM Subunit Elicits CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  15. Methanol Extract fromAntioxidants (Basel, Switzerland) · 2025
    Article
  16. Early cancer diagnosisWorld journal of gastrointestinal oncology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Galectin-4 potentiates CD8+ T cell immunity by enhancing MHC-I expression on dendritic cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
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

12 authors at 3 institutions in 2 countries.

Tommy LidströmWallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden.ORCID 0000-0002-1353-316X
Joshua CummingWallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden.ORCID 0000-0003-3661-7443
Rahul GaurWallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden.ORCID 0000-0003-0529-7176
Lars FrängsmyrDepartment of Clinical Microbiology, Umeå University, Umeå, Sweden.ORCID 0000-0002-6523-5156
Ioannis S Pateras2nd Department of Pathology, "Attikon" University Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-6406-9811
Matthias J MickertLumito AB, Lund, Sweden.ORCID 0000-0002-1542-5998
Oskar FranklinDepartment of Surgical and Perioperative Science, Umeå University, Umeå, Sweden.ORCID 0000-0002-3777-6887
Mattias N E ForsellDepartment of Clinical Microbiology, Umeå University, Umeå, Sweden.ORCID 0000-0001-6904-742X
Niklas ArnbergDepartment of Clinical Microbiology, Umeå University, Umeå, Sweden.ORCID 0000-0002-7069-6678
Mitesh DongreWallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden.ORCID 0000-0002-7151-1137
Cedric PattheyWallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden.ORCID 0000-0002-2627-9578
Daniel ÖhlundWallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden.ORCID 0000-0002-5847-2778
Umeå University · SENational and Kapodistrian University of Athens · GRSwedish Orphan Biovitrum (Sweden) · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is characterized by rich deposits of extracellular matrix (ECM), affecting the pathophysiology of the disease. Here, we identified galectin 4 (gal 4) as a cancer cell-produced protein that was deposited into the ECM of PDAC tumors and detected high-circulating levels of gal 4 in patients with PDAC. In orthotopic transplantation experiments, we observed increased infiltration of T cells and prolonged survival in immunocompetent mice transplanted with cancer cells with reduced expression of gal 4. Increased survival was not observed in immunodeficient RAG1-/- mice, demonstrating that the effect was mediated by the adaptive immune system. By performing single-cell RNA-sequencing, we found that the myeloid compartment and cancer-associated fibroblast (CAF) subtypes were altered in the transplanted tumors. Reduced gal 4 expression associated with a higher proportion of myofibroblastic CAFs and reduced numbers of inflammatory CAFs. We also found higher proportions of M1 macrophages, T cells, and antigen-presenting dendritic cells in tumors with reduced gal 4 expression. Using a coculture system, we observed that extracellular gal 4 induced apoptosis in T cells by binding N-glycosylation residues on CD3ε/δ. Hence, we show that gal 4 is involved in immune evasion and identify gal 4 as a promising drug target for overcoming immunosuppression in PDAC.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsAnimalsApoptosisGalectin 4Immune EvasionMiceGalectin 4

Identifiers

PMID36478037
PMCPMC9808371
OpenAlexW4310960003

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.