Evidence map›Paper›PMID 9337394›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1997

Quantitative trait loci for estrogen-dependent pituitary tumor growth in the rat.

D L Wendell, J Gorski

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 61 citations in OpenAlex.

  1. Mapping Mammary Tumor Traits in the Rat.Methods in molecular biology (Clifton, N.J.) · 2019
    Review
  2. Genetic variation in sensitivity to estrogens and breast cancer risk.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
  3. Article
  4. Article
  5. Article
  6. 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
  7. Toxicological sciences : an official journal of the Society of Toxicology · 2010
    Article
  8. Article
  9. Article
  10. Genetic control of estrogen action in the rat: mapping of QTLs that impact pituitary lactotroph hyperplasia in a BN x ACI intercross.Mammalian genome : official journal of the International Mammalian Genome Society · 2007
    Article
  11. Genetic mapping of loci controlling diethylstilbestrol-induced thymic atrophy in the Brown Norway rat.Mammalian genome : official journal of the International Mammalian Genome Society · 2006
    Article
  12. Genetic identification of distinct loci controlling mammary tumor multiplicity, latency, and aggressiveness in the rat.Mammalian genome : official journal of the International Mammalian Genome Society · 2006
    Article
  13. Angiogenesis and capillary maturation phenotypes associated with the Edpm3 locus on rat chromosome 3.Mammalian genome : official journal of the International Mammalian Genome Society · 2006
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

2 authors at 1 institution in 1 country.

D L WendellDepartment of Biochemistry, University of Wisconsin-Madison 53706-1569, USA.
J Gorski
University of Wisconsin–Madison · US

Funding

CONTROL OF ESTROGEN INDUCED PITUITARY HYPERPLASIAF32CA067422 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI WENDELL, DOUGLAS L · 1995 to 1996
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ESTROGEN INDUCTION OF PITUITARY HYPERPLASIAR01CA058013 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI GORSKI, JACK · 1992 to 1996
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ESTROGEN-DEPENDENT TUMOR GROWTH AND ANGIOGENESISR01CA071911 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI GORSKI, JACK · 1996 to 1999
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NCI NIH HHS CA58013NCI NIH HHS CA67422NCI NIH HHS CA71911-01
6 · The paper itself

Abstract

Growth control is of fundamental importance to biology in general and of critical importance to cancer research in particular. Tumors develop when control of the normal growth process is lost. The rat pituitary is a model system for control of estrogen-dependent growth. Chronic estrogen treatment induces uncontrolled growth in the pituitaries of Fischer 344 (F344) rats, but not of Brown Norway (BN) rats. We have identified five quantitative trait loci (QTL) for estrogen-dependent pituitary mass (Edpm) in an F2 intercross of F344 and BN. These QTL reside on rat Chromosomes (Chrs) 2, 3, 5, and 9 and explain a total of 55% of the genetic variance in the F2. We have also detected suggestive evidence for a QTL on rat Chr 14. For Edpm2-1, Edpm2-2, Edpm3, and Edpm5, the F344 allele corresponds with increased pituitary mass, as expected. Surprisingly, for Edpm9 and the suggested QTL on Chr 14, the BN allele corresponds with increased pituitary mass. We also find evidence for interaction (epistasis) between Edpm3 and Edpm9 and between Edpm5 and the suggested QTL on Chr 14.

Indexed as

EstrogensQuantitative Trait, HeritableAllelesAnimalsCell DivisionChromosome MappingCrosses, GeneticDiethylstilbestrolEpistasis, GeneticFemaleGenetic MarkersNeoplasms, Hormone-DependentPituitary NeoplasmsRatsRats, Inbred BNRats, Inbred F344DiethylstilbestrolEstrogensGenetic Markers

Identifiers

PMID9337394
OpenAlexW2029746280

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.