Evidence map›Paper›PMID 40172096›Full record

ArticleJournal of neurochemistry2025

Impact of Psychological Stress and Spontaneous Tumour Regression on the Hippocampal Proteome in a Mouse Model of Breast Cancer.

Myrthe Mampay, Gheed Al-Hity, Sara O Rolle, Walla Alzboon, Nicolas A Stewart, Melanie S Flint, Graham K Sheridan

Abstract read
In one paragraph

Article in Journal of neurochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

7 authors.

Myrthe MampaySchool of Applied Sciences, University of Brighton, Brighton, UK.
Gheed Al-HitySchool of Applied Sciences, University of Brighton, Brighton, UK.
Sara O RolleGreen Templeton College, University of Oxford, Oxford, UK.
Walla AlzboonSchool of Life Sciences, University of Nottingham, Nottingham, UK.
Nicolas A StewartSchool of Applied Sciences, University of Brighton, Brighton, UK.
Melanie S FlintSchool of Applied Sciences, University of Brighton, Brighton, UK.
Graham K SheridanSchool of Life Sciences, University of Nottingham, Nottingham, UK.ORCID 0000-0002-8493-2651

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cognitive impairment is common in people diagnosed with breast cancer, but the molecular mechanisms that underlie maladaptive changes in the brain are unknown. The psychological stress of a cancer diagnosis is certainly a contributing factor. Here, we investigated alterations in the hippocampal proteome in response to both cancer and psychological stress using label-free quantitative mass spectrometry techniques. An orthotopic syngeneic model of triple-negative breast cancer (TNBC) was established by injecting Py230 cells into the mammary fat pads of female C57Bl/6 mice. Half of the mice were subjected to a daily restraint stress paradigm. Mice that experienced both cancer and restraint stress lost weight and displayed larger tumours compared to non-stressed mice. Their urinary corticosterone levels were also elevated, as measured by enzyme-linked immunosorbent assay. Non-stressed tumour-bearing mice displayed higher levels of TNFα in the prefrontal cortex (PFC) compared to stressed mice with cancer. Flow cytometry results suggested that the CD4

Indexed as

HippocampusProteomeStress, PsychologicalTriple Negative Breast NeoplasmsAnimalsCell Line, TumorDisease Models, AnimalFemaleMiceMice, Inbred C57BLProteomebreast cancercytokineshippocampusproteomicsstresstumour regression

Identifiers

PMID40172096
PMCPMC11963485

What Socratic 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 Socratic graph.