Evidence map›Paper›PMID 41097775›Full record

ReviewCancers2025

Guardians in the Gut: Mechanistic Insights into a Hidden Ally Against Triple-Negative Breast Cancer.

Kayla Jaye, Muhammad A Alsherbiny, Dennis Chang, Chun-Guang Li, Deep Jyoti Bhuyan

Abstract readReview
In one paragraph

Review in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

5 authors.

Kayla JayeNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.ORCID 0000-0001-7809-3401
Muhammad A AlsherbinyNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.ORCID 0000-0001-9337-2441
Dennis ChangNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.
Chun-Guang LiNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.ORCID 0000-0002-7789-2209
Deep Jyoti BhuyanNICM Health Research Institute, Western Sydney University, Penrith, NSW 2751, Australia.ORCID 0000-0002-9736-0197

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiome possesses a diverse range of biological properties that play a role in maintaining host health and preventing disease. Gut microbial metabolites, including short-chain fatty acids, natural purine nucleosides, ellagic acid derivatives, and tryptophan metabolites, have been observed to have complex and multifaceted roles in the gut and in wider body systems in the management of disease, including cancer. Triple-negative breast cancer is the most aggressive subtype of breast cancer, with restricted treatment options and poor prognoses. Recently, preclinical research has investigated the antiproliferative potential of gut microbial metabolites against this type of breast cancer with promising results. However, little is understood about the mechanisms of action and molecular pathways driving this antiproliferative potential. Understanding the complex mechanisms of action of gut microbial metabolites on triple-negative breast cancer will be instrumental in the investigation of the combined administration with standard chemotherapeutic drugs. To date, there is a paucity of research studies investigating the potential synergistic interactions between gut microbial metabolites and standard chemotherapeutic drugs. The identification of synergistic potential between these compounds may provide alternate and more effective therapeutic options in the treatment and management of triple-negative breast cancer. Further investigation into the mechanistic action of gut microbial metabolites against this breast cancer subtype may support the administration of more cost-effective treatment options for breast cancer, with an aim to reduce side effects associated with standard treatments. Additionally, future research will aim to identify more potent metabolite-drug combinations in the mitigation of triple-negative breast cancer progression and metastasis.

Indexed as

ellagic acid derivativesgut microbial metabolitesnatural purine nucleosidesshort-chain fatty acidsstandard chemotherapytriple-negative breast cancertryptophan metabolites

Identifiers

PMID41097775
PMCPMC12523523

What OpenQuestion holds

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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.