Evidence map›Paper›PMID 25482952›Full record

ArticleCancer biology & therapy2014

Dose-dependent benefits of quercetin on tumorigenesis in the C3(1)/SV40Tag transgenic mouse model of breast cancer.

Jl Steiner, Jm Davis, Jl McClellan, Rt Enos, Ja Carson, R Fayad, M Nagarkatti, Ps Nagarkatti, D Altomare, Ke Creek and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.2field-weighted citation impact, top 23% of its field
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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. Hawthorn (Molecules (Basel, Switzerland) · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Sub-chronic oral toxicity screening of quercetin in mice.BMC complementary medicine and therapies · 2022
    Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Therapy-related acute myeloid leukemia and its prevention.American journal of blood research · 2020
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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 at 2 institutions in 1 country.

Jl Steinera Department of Pathology Microbiology and Immunology ; University of South Carolina School of Medicine ; Columbia , SC USA.
Jm Davis
Jl McClellan
Rt Enos
Ja Carson
R Fayad
M Nagarkatti
Ps Nagarkatti
D Altomare
Ke Creek
Ea Murphy
University of South Carolina · USColumbia College - South Carolina · US

Funding

Targeting early ceramide elevation in pre-symptomatic eczemaP20GM103641 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI ENOS, REILLY, NAGARKATTI, PRAKASH S · 2012 to 2023
$20.7M
Use of Resveratrol to treat experimental multiple sclerosisP01AT003961 · NCCIH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI SINGH, NARENDRA P · 2007 to 2018
$14.2M
Role of natural indoles in experimental autoimmune encephalomyelitisR01AT006888 · NCCIH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI · 2011 to 2015
$2.0M
Estrogen-T cell InteractionsR01ES019313 · NIEHS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI, NAGARKATTI, PRAKASH S · 2010 to 2014
$1.5M
Regulation of Macrophages in Obesity-Enhanced Colon Cancer:Benefits of QuercetinK01AT007824 · NCCIH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI MURPHY, ELIZABETH ANGELA · 2013 to 2017
$632k
NCCIH NIH HHS K01 AT007824NCCIH NIH HHS K01AT007824NCCIH NIH HHS P01 AT003961NCCIH NIH HHS R01 AT006888NIEHS NIH HHS R01 ES019313NIGMS NIH HHS P20 GM103641NIGMS NIH HHS P20GM103641
6 · The paper itself

Abstract

Breast cancer is the leading cause of cancer related death in women. Quercetin is a flavonol shown to have anti-carcinogenic actions. However, few studies have investigated the dose-dependent effects of quercetin on tumorigenesis and none have used the C3(1)/SV40 Tag breast cancer mouse model. At 4 weeks of age female C3(1)/SV40 Tag mice were randomized to one of four dietary treatments (n = 15-16/group): control (no quercetin), low-dose quercetin (0.02% diet), moderate-dose quercetin (0.2% diet), or high-dose quercetin (2% diet). Tumor number and volume was assessed twice a week and at sacrifice (20 wks). Results showed an inverted 'U' dose-dependent effect of dietary quercetin on tumor number and volume; at sacrifice the moderate dose was most efficacious and reduced tumor number 20% and tumor volume 78% compared to control mice (C3-Con: 9.0 ± 0.9; C3-0.2%: 7.3 ± 0.9) and (C3-Con: 2061.8 ± 977.0 mm(3); and C3-0.2%: 462.9 ± 75.9 mm(3)). Tumor volume at sacrifice was also reduced by the moderate dose compared to the high and low doses (C3-2%: 1163.2 ± 305.9 mm(3); C3-0.02%: 1401.5 ± 555.6 mm(3)), as was tumor number (C3-2%: 10.7 ± 1.3 mm(3); C3-0.02%: 8.1 ± 1.1 mm(3)). Gene expression microarray analysis performed on mammary glands from C3-Con and C3-0.2% mice determined that 31 genes were down-regulated and 9 genes were up-regulated more than 2-fold (P < 0.05) by quercetin treatment. We report the novel finding that there is a distinct dose-dependent effect of quercetin on tumor number and volume in a transgenic mouse model of human breast cancer, which is associated with a specific gene expression signature related to quercetin treatment.

Indexed as

AnimalsAnticarcinogenic AgentsBreast NeoplasmsCell Transformation, NeoplasticChemopreventionDisease Models, AnimalDose-Response Relationship, DrugFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMammary Neoplasms, ExperimentalMiceMice, TransgenicQuercetinTime FactorsAnticarcinogenic AgentsQuercetinBW, body weightDCIS, ductal carcinoma in situDEPTOR, DEP domain containing mTOR-interacting proteinDEXA, dual-energy X-ray absorptiometrydose-responseERα, estrogen receptor alphaFABP7, fatty acid binding protein-7flavonoidgene expression microarrayGREB1, growth regulation by estrogen in breast cancerkrt6a/b, keratin 6A/Bmammary tumorigenesisMIN, mammary intraepithelial neoplasiaMuc13, Mucin 13NGFR, nerve growth factor receptorTIMP4, tissue inhibitor of metalloproteinases-4TMPRSS4, transmembrane protease serine 4

Identifiers

PMID25482952
PMCPMC4623114
OpenAlexW2035603238

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.