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1251 Impact of intra-tumoral mammary microbiota on macrophage biology and anti-tumor immune response in breast cancer

2025· article· W4415898595 on OpenAlexaff
Sara Haije

Bibliographic record

VenueRegular and Young Investigator Award Abstracts · 2025
Typearticle
Language
FieldImmunology and Microbiology
TopicImmune cells in cancer
Canadian institutionsCentre Hospitalier de l’Université de MontréalCentre hospitalier universitaire de Québec
Fundersnot available
KeywordsImmune systemMacrophageBreast cancerMammary glandCancerMammary tumor

Abstract

fetched live from OpenAlex

Background In recent decades, a revolution in knowledge about the human gut microbiota has shed light on the major role of commensal bacteria in carcinogenesis, tumor progression, and the response to immunotherapy. We now know that bacteria can infiltrate various solid tumors and form a local microbiota in breast cancer. The discovery of this bacterial population has opened a new area of research into the intra-tumoral breast microbiota and its role in the tumor microenvironment (TME), particularly regarding immune content. Our laboratory detected, using immunohistochemistry on human breast tumor sections, the presence of macrophages carrying bacterial components such as lipopolysaccharide (LPS). A positive correlation was also observed between the abundance of intra-tumoral bacteria and long-term survival in patients with advanced-grade or stage breast cancer. However, at the fundamental level, the impact of these bacteria on tumor-associated immune responses and the TME remains poorly characterized in breast cancer. Considering the functional plasticity of macrophages and their prognostic significance in breast cancer, we hypothesize that certain bacterial species within the intra-tumoral breast microbiota may modulate macrophage biology, and consequently, anti-tumor immune responses, which could influence the response to immunotherapy.Methods We aimed to determine the impact of heat-inactivated bacteria ( E. coli and S. epidermidis) on the polarization phenotype of macrophages and their effect on tumors. To this end, we differentiated blood monocytes into macrophages and co-cultured them with breast cancer cell lines (MDA-MB-231, BT549, T47D, SKBR3) expressing green fluorescent protein (GFP) at the nuclear level. The macrophages were exposed to components of Gram-negative bacteria, such as LPS, or to bacteria in combination with interferon-gamma (IFN-γ).Results Based on the results obtained by fluorescent microscopy, E. coli stimulation led to a reduction in tumor cell numbers when co-cultured with macrophages. In contrast, S. epidermidis did not show any significant effect on tumor cell numbers. From a phenotypic perspective, flow cytometry and multiplex cytokine assay results showed an increased expression of surface markers associated with the M1 phenotype, such as CD86, and elevated levels of several pro-inflammatory cytokines and chemokines, including TNF-α and CXCL10, in macrophages stimulated with E. coli bacteria.Conclusions Our results suggest that macrophages stimulated by heat-inactivated E. coli can be polarized towards the tumoricidal M1 phenotype. These findings provide insights into the potential of leveraging the intra-tumoral microbiota to reprogram macrophages and modulate immune responses, offering promising strategies for improving the efficacy of immunotherapy in breast cancer patients.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.007

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.007
GPT teacher head0.267
Teacher spread0.260 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
Admission routes1
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