Evidence map›Paper›PMID 31354733›Full record

ArticleFrontiers in immunology2019

The Tim-3-Galectin-9 Pathway and Its Regulatory Mechanisms in Human Breast Cancer.

Inna M Yasinska, Svetlana S Sakhnevych, Ludmila Pavlova, Anette Teo Hansen Selnø, Ana Maria Teuscher Abeleira, Ouafa Benlaouer, Isabel Gonçalves Silva, Marianne Mosimann, Luca Varani, Marco Bardelli and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

105 citing papers in PubMed, 1 synthesis or guideline pooled it, 170 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Galectin-9-An Emerging Glyco-Immune Checkpoint Target for Cancer Therapy.International journal of molecular sciences · 2025
    Review
  12. TIM3Cancer cell · 2025
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

45 more citing papers are in PubMed but not listed here.

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

19 authors at 8 institutions in 3 countries.

Inna M YasinskaMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Svetlana S SakhnevychMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Ludmila PavlovaSchool of Biological Sciences, University of Essex, Colchester, United Kingdom.
Anette Teo Hansen SelnøMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Ana Maria Teuscher AbeleiraDepartment of Pediatric Surgery, Department of Biomedical Research, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Ouafa BenlaouerMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Isabel Gonçalves SilvaMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Marianne MosimannDepartment of Pediatric Surgery, Department of Biomedical Research, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Luca VaraniInstitute for Research in Biomedicine, Universita' della Svizzera italiana, Bellinzona, Switzerland.
Marco BardelliInstitute for Research in Biomedicine, Universita' della Svizzera italiana, Bellinzona, Switzerland.
Rohanah HussainBeamline B23, Diamond Light Source, Didcot, United Kingdom.
Giuliano SiligardiBeamline B23, Diamond Light Source, Didcot, United Kingdom.
Dietmar CholewaDepartment of Pediatric Surgery, Department of Biomedical Research, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Steffen M BergerDepartment of Pediatric Surgery, Department of Biomedical Research, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Bernhard F GibbsMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Yuri A UshkaryovMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Elizaveta Fasler-KanDepartment of Pediatric Surgery, Department of Biomedical Research, Children's Hospital, Inselspital, University of Bern, Bern, Switzerland.
Elena KlenovaSchool of Biological Sciences, University of Essex, Colchester, United Kingdom.
Vadim V SumbayevMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Medway School of Pharmacy · GBDiamond Light Source · GBUniversità della Svizzera italiana · CHUniversity Children’s Hospital Bern · CHUniversity of Bern · CHUniversity of Essex · GBCarl von Ossietzky Universität Oldenburg · DEUniversity Hospital of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cancer cells operate a variety of effective molecular and signaling mechanisms which allow them to escape host immune surveillance and thus progress the disease. We have recently reported that the immune receptor Tim-3 and its natural ligand galectin-9 are involved in the immune escape of human acute myeloid leukemia (AML) cells. These cells use the neuronal receptor latrophilin 1 (LPHN1) and its ligand fibronectin leucine rich transmembrane protein 3 (FLRT3, and possibly other ligands) to trigger the pathway. We hypothesized that the Tim-3-galectin-9 pathway may be involved in the immune escape of cancer cells of different origins. We found that studied breast tumors expressed significantly higher levels of both galectin-9 and Tim-3 compared to healthy breast tissues of the same patients and that these proteins were co-localized. Increased levels of LPHN2 and expressions of LPHN3 as well as FLRT3 were also detected in breast tumor cells. Activation of this pathway facilitated the translocation of galectin-9 onto the tumor cell surface, however no secretion of galectin-9 by tumor cells was observed. Surface-based galectin-9 was able to protect breast carcinoma cells against cytotoxic T cell-induced death. Furthermore, we found that cell lines from brain, colorectal, kidney, blood/mast cell, liver, prostate, lung, and skin cancers expressed detectable amounts of both Tim-3 and galectin-9 proteins. The majority of cell lines expressed one of the LPHN isoforms and FLRT3. We conclude that the Tim-3-galectin-9 pathway is operated by a wide range of human cancer cells and is possibly involved in prevention of anti-tumor immunity.

Indexed as

Breast NeoplasmsCell Line, TumorFemaleGalectinsHepatitis A Virus Cellular Receptor 2HumansLeukemia, Myeloid, AcuteMCF-7 CellsMembrane GlycoproteinsReceptors, G-Protein-CoupledSignal TransductionT-Lymphocytes, CytotoxicGalectinsHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2LGALS9 protein, humanMembrane GlycoproteinsReceptors, G-Protein-Coupledbreast cancergalectin-9immune evasionimmune surveillanceTIM-3

Identifiers

PMID31354733
PMCPMC6637653
OpenAlexW2957946774

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.