Evidence map›Paper›PMID 40713647›Full record

ArticleBreast cancer research : BCR2025

Short-term consumption of the modified standard American diet perturbed the metabolic balance and altered DNA damage in MMTV-PyMT transgenic mice.

Arlet Hernandez, Alekhya Puppala, Jenna Hedlich-Dwyer, Nayonika Mukherjee, Guihua Zhai, Valeria L Dal Zotto, Bohan Ning, Hua Guo, Ritu Aneja, Natalie R Gassman

Abstract read
In one paragraph

Article in Breast cancer research : BCR, 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

10 authors.

Arlet HernandezDepartment of Pharmacology and Toxicology, Heersink School of Medicine, The University of Alabama at Birmingham, 1720 University Blvd, Birmingham, AL, 35294, USA.
Alekhya PuppalaDepartment of Nutrition Sciences, School of Health Professions, The University of Alabama at Birmingham, 1716 9th Ave South, Birmingham, AL, 35294, USA.
Jenna Hedlich-DwyerDepartment of Pharmacology and Toxicology, Heersink School of Medicine, The University of Alabama at Birmingham, 1720 University Blvd, Birmingham, AL, 35294, USA.
Nayonika MukherjeeDepartment of Pharmacology and Toxicology, Heersink School of Medicine, The University of Alabama at Birmingham, 1720 University Blvd, Birmingham, AL, 35294, USA.
Guihua ZhaiCenter for Clinical and Translational Sciences, Biostatistics, Epidemiology & Research Design, The University of Alabama at Birmingham, 1825 University Blvd, Birmingham, AL, 35294, USA.
Valeria L Dal ZottoDepartment of Pathology, Heersink School of Medicine, The University of Alabama at Birmingham, 1802 6th Ave South, Birmingham, AL, 35233, USA.
Bohan NingDepartment of Pathology, Heersink School of Medicine, The University of Alabama at Birmingham, 1802 6th Ave South, Birmingham, AL, 35233, USA.
Hua GuoDepartment of Pathology, Heersink School of Medicine, The University of Alabama at Birmingham, 1802 6th Ave South, Birmingham, AL, 35233, USA.
Ritu AnejaDepartment of Nutrition Sciences, School of Health Professions, The University of Alabama at Birmingham, 1716 9th Ave South, Birmingham, AL, 35294, USA.
Natalie R GassmanDepartment of Pharmacology and Toxicology, Heersink School of Medicine, The University of Alabama at Birmingham, 1720 University Blvd, Birmingham, AL, 35294, USA. nrg2@uab.edu.

Funding

National Dissemination of I-Corps@NCATS: Accelerating Translation through CommercializationUL1TR003096 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GUTIERREZ, ORLANDO M, KIMBERLY, ROBERT P. · 2019 to 2023
$43.6M
CTSA UM1 at the University of Alabama at BirminghamUM1TR004771 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PATRICE DELAFONTAINE, Orlando M Gutierrez · 2024 to 2026
$29.2M
TRAINING AND CAREER DEVELOPMENTU54CA118948 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI UPENDER MANNE, Erica Michelle Stringer-Reasor · 2005 to 2026
$26.6M
NCATS NIH HHS TL1R003106NCATS NIH HHS UL1TR003096NCATS NIH HHS UM1TR004771NCI NIH HHS U54 CA118948
6 · The paper itself

Abstract

backgroundRisk factors for breast cancer include obesity and hyperglycemia, which are associated with poor survival. Previous studies have used high-fat diets (HFDs) or Western-style diets to model dietary influences on breast cancer progression. However, these diets do not reflect the energy-dense, nutrient-poor diets that Americans typically consume. To address this gap in our understanding of the interplay between diet and breast cancer progression, we examined the effects of a modified standard American diet (SAD2) on mammary tumorigenesis in the MMTV-PyMT transgenic murine model and their FVB/N controls.

methodsMMTV-PyMT and FVB/N mice were fed normal chow or the experimental diet SAD2 for up to 12 weeks. We evaluated body weight, blood glucose, adiposity, cytokine, and tumor characteristics to measure SAD2 diet-induced changes in breast tumor development.

resultsIncreased body weight and adiposity were observed in MMTV SAD2-treated mice, consistent with the findings of shorter-term HFD studies. The SAD2 diet also resulted in earlier tumor initiation and progression and decreased survival in the SAD2-fed mice. While only modest changes were observed in circulating cytokines and metabolic parameters, the SAD2 tumors presented significant changes in oxidative DNA damage and advanced glycation end products (AGEs). These changes coincided with increases in the oncogenic transcription factor Foxm1 and the expression of Glut1. Both proteins are elevated in breast cancer patient samples but have not yet been linked to diet-induced effects.

conclusionsUsing SAD2, we demonstrated that an American-style diet increased weight and adiposity while promoting the accumulation of oxidative DNA damage and AGEs and the expression of oncogenic Foxm1 within a relatively short diet interval. These data suggest that the SAD2 diet may offer insight into mechanisms that promote breast cancer aggressiveness and resistance to therapy.

Indexed as

Breast NeoplasmsDietDiet, High-FatDNA DamageMammary Neoplasms, ExperimentalAdiposityAnimalsBody WeightDisease Models, AnimalFemaleHumansMammary Tumor Virus, MouseMiceMice, TransgenicAdiposityAmerican dietBreast cancerDNA damageFoxm1Oxidative stress

Identifiers

PMID40713647
PMCPMC12296626

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LicenceCC BY
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Registered trials

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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.