Evidence map›Paper›PMID 15611180›Full record

ArticleGenetics2004

Genetic determination of susceptibility to estrogen-induced mammary cancer in the ACI rat: mapping of Emca1 and Emca2 to chromosomes 5 and 18.

Karen A Gould, Martin Tochacek, Beverly S Schaffer, Tanya M Reindl, Clare R Murrin, Cynthia M Lachel, Eric A VanderWoude, Karen L Pennington, Lisa A Flood, Kimberly K Bynote and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.8field-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

35 citing papers in PubMed, 53 citations in OpenAlex.

  1. Endocrine-disrupting compounds and metabolomic reprogramming in breast cancer.Journal of biochemical and molecular toxicology · 2023
    Review
  2. Article
  3. Review
  4. Article
  5. Mapping Mammary Tumor Traits in the Rat.Methods in molecular biology (Clifton, N.J.) · 2019
    Review
  6. Review
  7. Genetic variation in sensitivity to estrogens and breast cancer risk.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Ept7 influences estrogen action in the pituitary gland and body weight of rats.Mammalian genome : official journal of the International Mammalian Genome Society · 2014
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

13 authors at 3 institutions in 1 country.

Karen A GouldEppley Institute for Research in Cancer, Department of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska 68198-5805, USA.
Martin Tochacek
Beverly S Schaffer
Tanya M Reindl
Clare R Murrin
Cynthia M Lachel
Eric A VanderWoude
Karen L Pennington
Lisa A Flood
Kimberly K Bynote
Jane L Meza
Michael A Newton
James D Shull
Pediatrics and Genetics · USUniversity of Nebraska Medical Center · USUniversity of Wisconsin–Madison · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
GENETIC SUSCEPTIBILITY TO ESTROGEN INDUCED MAMMARY CAR01CA077876 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SHULL, JAMES D · 1998 to 2012
$4.4M
ESTROGENS, DIETARY ENERGY AND PITUITARY TUMORIGENESISR01CA068529 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SHULL, JAMES D · 1995 to 2002
$924k
STATISTICAL METHODS FOR MOLECULAR CANCER DATAR01CA064364 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI NEWTON, MICHAEL A · 2000 to 2006
$695k
NCI NIH HHS P30 CA036727NCI NIH HHS P30-CA36727NCI NIH HHS R01 CA064364NCI NIH HHS R01 CA077876NCI NIH HHS R01-CA64364NCI NIH HHS R01-CA68529NCI NIH HHS R01-CA77876
6 · The paper itself

Abstract

Hormonal, genetic, and environmental factors play major roles in the complex etiology of breast cancer. When treated continuously with 17beta-estradiol (E2), the ACI rat exhibits a genetically conferred propensity to develop mammary cancer. The susceptibility of the ACI rat to E2-induced mammary cancer appears to segregate as an incompletely dominant trait in crosses to the resistant Copenhagen (COP) strain. In both (ACI x COP)F(2) and (COP x ACI)F(2) populations, we find strong evidence for a major genetic determinant of susceptibility to E2-induced mammary cancer on distal rat chromosome 5. Our data are most consistent with a model in which the ACI allele of this locus, termed Emca1 (estrogen-induced mammary cancer 1), acts in an incompletely dominant manner to increase both tumor incidence and tumor multiplicity as well as to reduce tumor latency in these populations. We also find evidence suggestive of a second locus, Emca2, on chromosome 18 in the (ACI x COP)F(2) population. The ACI allele of Emca2 acts in a dominant manner to increase incidence and decrease latency. Together, Emca1 and Emca2 act independently to modify susceptibility to E2-induced mammary cancer.

Indexed as

Chromosome MappingGenetic Predisposition to DiseaseAnimalsEstradiolFemaleGenetic LinkageGenetic MarkersMammary Neoplasms, ExperimentalRatsRats, Inbred ACIEstradiolGenetic Markers

Identifiers

PMID15611180
PMCPMC1448731
OpenAlexW2134853046

What OpenQuestion holds

Textmetadata
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.