Evidence map›Paper›PMID 30718646›Full record

ArticleScientific reports2019

Cadaverine, a metabolite of the microbiome, reduces breast cancer aggressiveness through trace amino acid receptors.

Tünde Kovács, Edit Mikó, András Vida, Éva Sebő, Judit Toth, Tamás Csonka, Anita Boratkó, Gyula Ujlaki, Gréta Lente, Patrik Kovács and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed, 2 pooled it
7.2field-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

120 citing papers in PubMed, 2 syntheses or guidelines pooled it, 178 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Review
  7. Article
  8. The dialogue between breast cancer and microorganisms.Frontiers in cellular and infection microbiology · 2026
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Mammary Gland Microbiota in Benign Breast Diseases.International journal of molecular sciences · 2025
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Article

60 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

16 authors at 2 institutions in 2 countries.

Tünde KovácsDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Edit MikóDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
András VidaDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Éva SebőKenézy Breast Center, Kenézy Gyula County Hospital, Debrecen, 4032, Hungary.
Judit TothDepartment of Oncology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Tamás CsonkaDepartment of Pathology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Anita BoratkóDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Gyula UjlakiDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Gréta LenteDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Patrik KovácsDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Dezső TóthDepartment of Oncology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Péter ÁrkosyDepartment of Oncology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Borbála KissDepartment of Dermatology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Gábor MéhesDepartment of Pathology, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary.
James J GoedertNational Cancer Institute, National Institutes of Health, Bethesda, 20982 MD, USA.
Péter BaiDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Debrecen, 4032, Hungary. baip@med.unideb.hu.
University of Debrecen · HUNational Institutes of Health · US

Funding

Center for Strategic Scientific Initiatives, National Cancer Institute (NCI Center for Strategic Scientific Initiatives) Z01CP010214
6 · The paper itself

Abstract

Recent studies showed that changes to the gut microbiome alters the microbiome-derived metabolome, potentially promoting carcinogenesis in organs that are distal to the gut. In this study, we assessed the relationship between breast cancer and cadaverine biosynthesis. Cadaverine treatment of Balb/c female mice (500 nmol/kg p.o. q.d.) grafted with 4T1 breast cancer cells ameliorated the disease (lower mass and infiltration of the primary tumor, fewer metastases, and lower grade tumors). Cadaverine treatment of breast cancer cell lines corresponding to its serum reference range (100-800 nM) reverted endothelial-to-mesenchymal transition, inhibited cellular movement and invasion, moreover, rendered cells less stem cell-like through reducing mitochondrial oxidation. Trace amino acid receptors (TAARs), namely, TAAR1, TAAR8 and TAAR9 were instrumental in provoking the cadaverine-evoked effects. Early stage breast cancer patients, versus control women, had reduced abundance of the CadA and LdcC genes in fecal DNA, both responsible for bacterial cadaverine production. Moreover, we found low protein expression of E. coli LdcC in the feces of stage 1 breast cancer patients. In addition, higher expression of lysine decarboxylase resulted in a prolonged survival among early-stage breast cancer patients. Taken together, cadaverine production seems to be a regulator of early breast cancer.

Indexed as

MicrobiotaBreast NeoplasmsCadaverineCell Line, TumorCell MovementCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionFemaleHumansKaplan-Meier EstimateModels, BiologicalReceptors, Amino AcidCadaverineReceptors, Amino Acid

Identifiers

PMID30718646
PMCPMC6361949
OpenAlexW2914763919

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.