Evidence map›Paper›PMID 23574728›Full record

ArticleBMC veterinary research2013

The ESR1 gene is associated with risk for canine mammary tumours.

Kaja Sverdrup Borge, Malin Melin, Patricio Rivera, Stein Istre Thoresen, Matthew Thomas Webster, Henrik von Euler, Kerstin Lindblad-Toh, Frode Lingaas

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Is PTEN rs397510595 an Unexpected Guardian in Canine Mammary Neoplasia?International journal of molecular sciences · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Somatic Mutation ofCancers · 2019
    Article
  7. Article
  8. Canine mammary tumor risk is associated with polymorphisms in RAD51 and STK11 genes.Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc · 2018
    Article
  9. Review
  10. 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 4 institutions in 3 countries.

Kaja Sverdrup BorgeSection of Genetics, Department of Basic Sciences and Aquatic Medicine, Norwegian School of Veterinary Science, P,O Box 8146 Dep,, 0033 Oslo, Norway. KajaSverdrup.Borge@nvh.no
Malin Melin
Patricio Rivera
Stein Istre Thoresen
Matthew Thomas Webster
Henrik von Euler
Kerstin Lindblad-Toh
Frode Lingaas
Norwegian University of Life Sciences · NOUppsala University · SEScience for Life Laboratory · SESwedish University of Agricultural Sciences · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe limited within-breed genetic heterogeneity and an enrichment of disease-predisposing alleles have made the dog a very suitable model for the identification of genes associated with risk for specific diseases. Canine mammary cancer is an example of such a disease. However, the underlying inherited risk factors for canine mammary tumours (CMTs) are still largely unknown. In this study, 52 single nucleotide polymorphisms (SNPs) in ten human cancer-associated genes were genotyped in two different datasets in order to identify genes/alleles associated with the development of CMTs. The first dataset consisted of English Springer Spaniel (ESS) CMT cases and controls. ESS is a dog breed known to be at increased risk of developing CMTs. In the second dataset, dogs from breeds known to have a high frequency of CMTs were compared to dogs from breeds with a lower occurrence of these tumours.

resultsWe found significant associations to CMT for SNPs and haplotypes in the estrogen receptor 1 (ESR1) gene in the ESS material (best PBonf = 0.021). A large number of SNPs, among them several SNPs in ESR1, showed significantly different allele frequencies between the high and low risk breed groups (best PBonf = 8.8E-32, best PBPerm = 0.076).

conclusionsThe identification of CMT-associated SNPs in ESR1 in two independent datasets suggests that this gene might be involved in CMT development. These findings also support that CMT may serve as a good model for human breast cancer research.

Indexed as

AllelesAnimalsDog DiseasesDogsEstrogen Receptor alphaFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHaplotypesMammary Neoplasms, AnimalPolymorphism, Single NucleotideRisk FactorsSequence AlignmentEstrogen Receptor alpha

Identifiers

PMID23574728
PMCPMC3637093
OpenAlexW2163855624

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.