Evidence map›Paper›PMID 39410010›Full record

ArticleCancers2024

An Exogenous Ketone Ester Slows Tumor Progression in Murine Breast and Renal Cancer Models.

Henry Nnaemeka Ogbonna, Zachary Roberts, Nicholas Godwin, Pia Muri, William J Turbitt, Zoey N Swalley, Francesca R Dempsey, Holly R Stephens, Jianqing Zhang, Eric P Plaisance and 1 more

Abstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

11 authors.

Henry Nnaemeka OgbonnaGraduate Biomedical Sciences, Pathobiology, Pharmacology, and Physiology, University of Alabama at Birmingham, Birmingham, AL 35233, USA.ORCID 0000-0003-2740-1683
Zachary RobertsUndergraduate Science and Technology Honors Program, University of Alabama at Birmingham, Birmingham, AL 35233, USA.ORCID 0009-0000-2375-6968
Nicholas GodwinAlabama School of Fine Arts, Birmingham, AL 35233, USA.
Pia MuriDepartment of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
William J TurbittDepartment of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Zoey N SwalleyUndergraduate Honors College, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Francesca R DempseyGraduate Biomedical Sciences, Cancer Biology, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Holly R StephensGraduate Biomedical Sciences, Immunology, University of Alabama at Birmingham, Birmingham, AL 35233, USA.
Jianqing ZhangDepartment of Radiation Oncology, University of Alabama at Birmingham, Birmingham, AL 35233, USA.ORCID 0000-0001-5246-3371
Eric P PlaisanceDepartment of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL 35233, USA.ORCID 0000-0001-9621-6583
Lyse A NorianDepartment of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL 35233, USA.ORCID 0000-0003-1016-313X

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Why is the prevalence of obesity so high in U.S. Southern States? Regional predictors of BMI and obesity treatment response.P30DK056336 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI James O Hill · 2000 to 2026
$31.9M
UAB Pre-Doctoral Training Program in Obesity-Related ResearchT32HL105349 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARBARA A GOWER · 2010 to 2026
$5.7M
Overcoming obesity-associated immunotherapy resistance in renal cancerR01CA269568 · NCI · UNIVERSITY OF KENTUCKY · PI Lyse A Norian · 2023 to 2026
$2.1M
NCI NIH HHS P30 CA013148NCI NIH HHS R01 CA269568NHLBI NIH HHS T32 HL105349NIDDK NIH HHS P30 DK056336UAB O'Neal Invests Comprehensive Cancer Center grant to LAN an EP. FD is supported by a NHLBI pre-doctoral T32 (T32HL105349) fellowship. (T32HL105349)
6 · The paper itself

Abstract

BACKGROUND/

objectivesKetone esters (KEs) exhibit promise as anti-cancer agents but their impact on spontaneous metastases remains poorly understood. Although consumption of a ketogenic diet (KD) that is low in carbohydrates and high in fats can lead to KE production in vivo, the restrictive composition of KDs may diminish adherence in cancer patients.

methodsWe investigated the effects of an exogenous ketone ester-supplemented (eKET), carbohydrate-replete diet on tumor growth, metastasis, and underlying mechanisms in orthotopic models of metastatic breast (4T1-Luc) and renal (Renca-Luc) carcinomas. Mice were randomized to diet after tumor challenge.

resultsAdministration of KEs did not alter tumor cell growth in vitro. However, in mice, our eKET diet increased circulating β-hydroxybutyrate and inhibited primary tumor growth and lung metastasis in both models. Body composition analysis illustrated the overall safety of eKET diet use, although it was associated with a loss of fat mass in mice with renal tumors. Immunogenetic profiling revealed divergent intratumoral eKET-related changes by tumor type. In mammary tumors, Wnt and TGFβ pathways were downregulated, whereas in renal tumors, genes related to hypoxia and DNA damage repair were downregulated.

conclusionsThus, our eKET diet exerts potent antitumor and antimetastatic effects in both breast and renal cancer models, albeit with different modes of action and physiologic effects. Its potential as an adjuvant dietary approach for patients with diverse cancer types should be explored further.

Indexed as

breast cancerdietketone esterkidney cancer

Identifiers

PMID39410010
PMCPMC11476193

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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.