Evidence map›Paper›PMID 24196830›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2014

Metformin inhibits skin tumor promotion in overweight and obese mice.

L Allyson Checkley, Okkyung Rho, Joe M Angel, Jiyoon Cho, Jorge Blando, Linda Beltran, Stephen D Hursting, John DiGiovanni

Open access · bronzeAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Metformin: A Dual-Role Player in Cancer Treatment and Prevention.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
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  15. Review
  16. Article
  17. Obesity and Cancer: An Angiogenic and Inflammatory Link.Microcirculation (New York, N.Y. : 1994) · 2016
    Review
  18. Review
  19. Article
  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

8 authors at 1 institution in 1 country.

L Allyson CheckleyDell Pediatric Research Institute, The University of Texas at Austin, 1400 Barbara Jordan Blvd., Austin, TX 78723. john.digiovanni@austin.utexas.edu.
Okkyung Rho
Joe M Angel
Jiyoon Cho
Jorge Blando
Linda Beltran
Stephen D Hursting
John DiGiovanni
The University of Texas at Austin · US

Funding

Mechanisms of IGF-1 Tumor Promotion in Mouse SkinR01CA037111 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIGIOVANNI, JOHN · 1985 to 2010
$2.8M
Akt/mTOR Signaling in Energy Balance Modulation of Epithelial CarcinogenesisR01CA129409 · NCI · UNIVERSITY OF TEXAS AT AUSTIN · PI HURSTING, STEPHEN D · 2009 to 2013
$1.6M
NCI NIH HHS CA037111NCI NIH HHS CA129409NCI NIH HHS R01 CA037111NCI NIH HHS R01 CA129409
6 · The paper itself

Abstract

In the present study, the ability of metformin to inhibit skin tumor promotion by 12-O-tetradecanoylphorbol-13-acetate (TPA) was analyzed in mice maintained on either an overweight control diet or an obesity-inducing diet. Rapamycin was included for comparison, and a combination of metformin and rapamycin was also evaluated. Metformin (given in the drinking water) and rapamycin (given topically) inhibited development of both papillomas and squamous cell carcinomas in overweight and obese mice in a dose-dependent manner. A low-dose combination of these two compounds displayed an additive inhibitory effect on tumor development. Metformin treatment also reduced the size of papillomas. Interestingly, all treatments seemed to be at least as effective for inhibiting tumor formation in obese mice, and both metformin and rapamycin were more effective at reducing tumor size in obese mice compared with overweight control mice. The effect of metformin on skin tumor development was associated with a significant reduction in TPA-induced epidermal hyperproliferation. Furthermore, treatment with metformin led to activation of epidermal AMP-activated protein kinase (AMPK) and attenuated signaling through mTOR complex (mTORC)-1 and p70S6K. Combinations of metformin and rapamycin were more effective at blocking epidermal mTORC1 signaling induced by TPA consistent with the greater inhibitory effect on skin tumor promotion. Collectively, the current data demonstrate that metformin given in the drinking water effectively inhibited skin tumor promotion in both overweight and obese mice and that the mechanism involves activation of epidermal AMPK and attenuated signaling downstream of mTORC1.

Indexed as

Adenylate KinaseAdiponectinAnimalsBody WeightCarcinogenesisCarcinoma, Squamous CellDietDisease Models, AnimalDose-Response Relationship, DrugFemaleInsulinInsulin-Like Growth Factor ILeptinMechanistic Target of Rapamycin Complex 1MetforminMiceAdenylate KinaseAdiponectinInsulinInsulin-Like Growth Factor ILeptinMechanistic Target of Rapamycin Complex 1MetforminMultiprotein ComplexesRibosomal Protein S6 Kinases, 70-kDaSirolimusTetradecanoylphorbol AcetateTOR Serine-Threonine Kinases

Identifiers

PMID24196830
PMCPMC3918668
OpenAlexW2147685342

What OpenQuestion holds

Texttitle and abstract
LicenceTDM
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 OpenQuestion graph.