Evidence map›Paper›PMID 21484786›Full record

ArticleEuropean journal of immunology2011

ST2 deletion enhances innate and acquired immunity to murine mammary carcinoma.

Ivan Jovanovic, Gordana Radosavljevic, Maja Mitrovic, Vanda Lisnic Juranic, Andrew N J McKenzie, Nebojsa Arsenijevic, Stipan Jonjic, Miodrag L Lukic

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

75 citing papers in PubMed, 126 citations in OpenAlex.

  1. Review
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  6. Dual Role ofPharmaceuticals (Basel, Switzerland) · 2024
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  13. The role of IL-33/ST2 signaling in the tumor microenvironment and Treg immunotherapy.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
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  19. Review
  20. Dual role of interleukin-33 in tumors.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2021
    Article

15 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

8 authors at 3 institutions in 3 countries.

Ivan JovanovicCenter for Molecular Medicine and Stem Cell Research, Faculty of Medicine, University of Kragujevac, Kragujevac, Serbia.
Gordana Radosavljevic
Maja Mitrovic
Vanda Lisnic Juranic
Andrew N J McKenzie
Nebojsa Arsenijevic
Stipan Jonjic
Miodrag L Lukic
University of Kragujevac · RSUniversity of Rijeka · HRMRC Laboratory of Molecular Biology · GB

Funding

Medical Research Council MC_U105178805
6 · The paper itself

Abstract

ST2 is a member of the IL-1 receptor family and IL-33 was recently identified as its natural ligand. The IL-33/ST2 pathway regulates Th1/Th2 immune responses in autoimmune and inflammatory conditions, but the role of ST2 signaling in tumor growth and metastasis has not been investigated. We aimed to investigate whether ST2 gene deletion affects tumor appearance, growth, and metastasis, and antitumor immunity in an experimental metastatic breast cancer model. Deletion of ST2 in BALB/c mice bearing mammary carcinoma attenuated tumor growth and metastasis, which was accompanied by increased serum levels of IL-17, IFN-γ, and TNF-α and decreased IL-4. Tumor-bearing ST2-/- mice had significantly higher percentages of activated CD27high CD11bhigh NK cells, CD69+ and KLRG- NK cells and higher cytotoxic activity of splenocytes, NK cells, and CD8+ T cells in vitro. A significantly higher number of NK cells expressing IFN-γ were found in ST2-/- mice compared with WT recipients. In vivo depletion of CD8+ or NK cells revealed a key role for NK cells in enhanced antitumor immunity in ST2-/- mice. We report for the first time that suppressed breast cancer progression and metastasis in mice lacking ST2 corresponds mainly with enhanced cytotoxic activity of NK cells, and increased systemic Th1/Th17 cytokines.

Indexed as

Adaptive ImmunityImmunity, InnateAnimalsAntigens, CDAntigens, Differentiation, T-LymphocyteCD11b AntigenCD69 AntigensCD8-Positive T-LymphocytesCell Line, TumorDisease ProgressionFemaleInterferon-gammaInterleukin-17Interleukin-1 Receptor-Like 1 ProteinInterleukin-33Interleukin-4Antigens, CDAntigens, Differentiation, T-LymphocyteCD11b AntigenCD69 AntigensIl1rl1 protein, mouseIl33 protein, mouseInterferon-gammaInterleukin-17Interleukin-1 Receptor-Like 1 ProteinInterleukin-33Interleukin-4InterleukinsKlrg1 protein, mouseLectins, C-TypeReceptors, ImmunologicReceptors, InterleukinTumor Necrosis Factor-alphaTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID21484786
PMCPMC3746127
OpenAlexW2091617195

What OpenQuestion holds

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LicenceCC BY
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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.