Evidence map›Paper›PMID 21600785›Full record

ArticleCytokine2011

Benefits of exercise training on breast cancer progression and inflammation in C3(1)SV40Tag mice.

E A Murphy, J M Davis, T L Barrilleaux, J L McClellan, J L Steiner, M D Carmichael, M M Pena, J R Hebert, J E Green

Open access · greenAbstract read
In one paragraph

Article in Cytokine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 16% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  9. Article
  10. AnHeliyon · 2022
    Article
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  12. Review
  13. Insulin and cancer: a tangled web.The Biochemical journal · 2022
    Review
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  16. Article
  17. Article
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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

9 authors at 2 institutions in 1 country.

E A MurphyDepartment of Pathology, Microbiology & Immunology, School of Medicine, University of South Carolina, Columbia, SC 29209, United States. angela.murphy@uscmed.sc.edu
J M Davis
T L Barrilleaux
J L McClellan
J L Steiner
M D Carmichael
M M Pena
J R Hebert
J E Green
University of South Carolina · USNational Cancer Institute · US

Funding

Transgenic Models for Prostate and Breast CancerZIABC005740 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GREEN, JEFFREY E · 2009 to 2016
$7.8M
Stromal modulation of response to Thymidylate synthase inhibitorsR01CA154731 · NCI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI PENA, MARIA MARJORETTE · 2011 to 2015
$1.5M
Expanding Mentoring Capacity in High-Risk PopulationsK05CA136975 · NCI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI HEBERT, JAMES R · 2009 to 2013
$801k
Intramural NIH HHSNCI NIH HHS K05 CA136975NCI NIH HHS R01 CA154731
6 · The paper itself

Abstract

Many observational epidemiologic studies suggest an association between exercise and breast cancer risk. However, the lack of controlled experimental studies that examine this relationship and the mechanisms involved weaken the basis for inferring a causal relationship. Inflammation plays a role in breast cancer progression and exercise has been reported to reduce inflammation; however, the anti-inflammatory effects of exercise in breast cancer have yet to be established. We examined the relationship between exercise training and systemic inflammation in relation to breast cancer progression in C3(1)SV40Tag mice. Female C3(1)SV40Tag mice were assigned to either exercise (Ex) or sedentary (Sed) treatment (n=12-14/group). Beginning at 4 wks of age mice (Ex) were run on a treadmill for 60 min/d (20 m/min and 5% grade), 6 d/wk for a period of 20 wks. Mice were examined weekly for palpable tumors, and tumor number and volume were recorded. At 24 wks of age mice were sacrificed and a more direct measure of tumor number and volume, and spleen weight was recorded. Plasma was analyzed for MCP-1 and IL-6 concentration using ELISA. Ex reduced palpable tumor number at sacrifice (24 wks) by approximately 70% (P<0.05). Tumor volume was also reduced in Ex at 21-23 wks (P<0.05). This reduction in tumor progression by Ex was associated with a reduction in plasma concentration of MCP-1 and IL-6, and spleen weight (P<0.05). These data provide strong support for a beneficial effect of exercise training on tumor progression in the C3(1)SV40Tag mouse model of breast cancer that may be partly mediated by its anti-inflammatory potential.

Indexed as

Disease ProgressionPhysical Conditioning, AnimalAnimalsBiomarkers, TumorBody WeightBreast NeoplasmsEatingFemaleInflammationMaleMiceMice, TransgenicRandom AllocationSpleenBiomarkers, Tumor

Identifiers

PMID21600785
PMCPMC3383660
OpenAlexW2090506708

What OpenQuestion holds

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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.