Evidence map›Paper›PMID 30934972›Full record

ReviewCells2019

Microbiome-Microbial Metabolome-Cancer Cell Interactions in Breast Cancer-Familiar, but Unexplored.

Edit Mikó, Tünde Kovács, Éva Sebő, Judit Tóth, Tamás Csonka, Gyula Ujlaki, Adrienn Sipos, Judit Szabó, Gábor Méhes, Péter Bai

Abstract readReview
In one paragraph

Review in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

133 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  17. Fecal sample biobanking for breast cancer research focused on the gut microbiome.medRxiv : the preprint server for health sciences · 2025
    Article
  18. Article
  19. Mammary Gland Microbiota in Benign Breast Diseases.International journal of molecular sciences · 2025
    Review
  20. Article

73 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

10 authors.

Edit MikóDepartment of Medical Chemistry, University of Debrecen, 4032 Debrecen, Hungary. miko.edit@med.unideb.hu.
Tünde KovácsDepartment of Medical Chemistry, University of Debrecen, 4032 Debrecen, Hungary. tunde.kovacs33@gmail.com.
Éva SebőKenézy Breast Center, Kenézy Gyula County Hospital, 4032 Debrecen, Hungary. seboeva@gmail.com.
Judit TóthKenézy Breast Center, Kenézy Gyula County Hospital, 4032 Debrecen, Hungary. tothjuditdr11@t-online.hu.
Tamás CsonkaDepartment of Pathology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary. csonkatamas84@gmail.com.
Gyula UjlakiDepartment of Medical Chemistry, University of Debrecen, 4032 Debrecen, Hungary. ujlakigyula15@gmail.com.
Adrienn SiposDepartment of Medical Chemistry, University of Debrecen, 4032 Debrecen, Hungary. siposadri@med.unideb.hu.
Judit SzabóDepartment of Microbiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary. szabjud@med.unideb.hu.
Gábor MéhesDepartment of Pathology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary. gabor.mehes@med.unideb.hu.
Péter BaiDepartment of Medical Chemistry, University of Debrecen, 4032 Debrecen, Hungary. baip@med.unideb.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is a leading cause of death among women worldwide. Dysbiosis, an aberrant composition of the microbiome, characterizes breast cancer. In this review we discuss the changes to the metabolism of breast cancer cells, as well as the composition of the breast and gut microbiome in breast cancer. The role of the breast microbiome in breast cancer is unresolved, nevertheless it seems that the gut microbiome does have a role in the pathology of the disease. The gut microbiome secretes bioactive metabolites (reactivated estrogens, short chain fatty acids, amino acid metabolites, or secondary bile acids) that modulate breast cancer. We highlight the bacterial species or taxonomical units that generate these metabolites, we show their mode of action, and discuss how the metabolites affect mitochondrial metabolism and other molecular events in breast cancer. These metabolites resemble human hormones, as they are produced in a "gland" (in this case, the microbiome) and they are subsequently transferred to distant sites of action through the circulation. These metabolites appear to be important constituents of the tumor microenvironment. Finally, we discuss how bacterial dysbiosis interferes with breast cancer treatment through interfering with chemotherapeutic drug metabolism and availability.

Indexed as

Cell CommunicationMetabolomeMicrobiotaAntineoplastic AgentsBreast NeoplasmsDysbiosisFemaleHumansAntineoplastic Agentsbreast cancercadaverineestrogen deconjugationFFARlithocholic acidmicrobiomemitochondrial metabolismOXPHOSsecondary bile acidsTAARTGR5

Identifiers

PMID30934972
PMCPMC6523810

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.