Evidence map›Paper›PMID 23408836›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Cancer-produced metabolites of 5-lipoxygenase induce tumor-evoked regulatory B cells via peroxisome proliferator-activated receptor α.

Katarzyna Wejksza, Catalina Lee-Chang, Monica Bodogai, Jessica Bonzo, Frank J Gonzalez, Elin Lehrmann, Kevin Becker, Arya Biragyn

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

68 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
  2. Autocrine CysLTOncogene · 2026
    Article
  3. Article
  4. Review
  5. Regulatory B cells andBiomolecules & biomedicine · 2026
    Article
  6. Review
  7. Review
  8. Regulatory B Cells in Tumor Microenvironment.Current issues in molecular biology · 2026
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Immune Checkpoints in B Cells: Unlocking New Potentials in Cancer Treatment.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  19. Review
  20. Review

8 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 1 country.

Katarzyna WejkszaImmunoregulation Section, Laboratory of Molecular Biology and Immunology, National Institute on Aging, Baltimore, MD 21224, USA.
Catalina Lee-Chang
Monica Bodogai
Jessica Bonzo
Frank J Gonzalez
Elin Lehrmann
Kevin Becker
Arya Biragyn
National Institute on Aging · USCenter for Cancer Research · USNational Cancer Institute · US

Funding

Xenobiotic ReceptorsZIABC005708 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GONZALEZ, FRANK J · 2009 to 2025
$16.4M
Analysis of complex biological systems by microarray based gene expressionZICAG000616 · NIA · NATIONAL INSTITUTE ON AGING · PI DE, SUPRIYO · 2009 to 2025
$15.5M
The role of immunosuppressive cells in metastasisZIAAG000443 · NIA · NATIONAL INSTITUTE ON AGING · PI BIRAGYN, ARYA · 2009 to 2022
$8.6M
Intramural NIH HHS ZIA AG000443
6 · The paper itself

Abstract

Breast cancer cells facilitate distant metastasis through the induction of immunosuppressive regulatory B cells, designated tBregs. We report in this study that, to do this, breast cancer cells produce metabolites of the 5-lipoxygenase pathway such as leukotriene B4 to activate the peroxisome proliferator-activated receptor α (PPARα) in B cells. Inactivation of leukotriene B4 signaling or genetic deficiency of PPARα in B cells blocks the generation of tBregs and thereby abrogates lung metastasis in mice with established breast cancer. Thus, in addition to eliciting fatty acid oxidation and metabolic signals, PPARα initiates programs required for differentiation of tBregs. We propose that PPARα in B cells and/or tumor 5-lipoxygenase pathways represents new targets for pharmacological control of tBreg-mediated cancer escape.

Indexed as

AnimalsB-Lymphocyte SubsetsCell Line, TumorCells, CulturedFemaleLipoxygenaseMelanoma, ExperimentalMiceMice, 129 StrainMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutNeoplasm MetastasisPPAR alphaTumor EscapeLipoxygenasePPAR alpha

Identifiers

PMID23408836
PMCPMC3594535
OpenAlexW2161001354

What OpenQuestion holds

Textmetadata
LicenceTDM
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.