Evidence map›Paper›PMID 19168544›Full record

ArticleHuman molecular genetics2009

Deletion of eIF2beta suppresses testicular cancer incidence and causes recessive lethality in agouti-yellow mice.

Jason D Heaney, Megan V Michelson, Kirsten K Youngren, Man-Yee J Lam, Joseph H Nadeau

Open access · greenAbstract read
In one paragraph

Article in Human molecular genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 14% 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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  8. Prognostic prediction and gene regulation network ofJournal of gastrointestinal oncology · 2021
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  19. Parent-of-origin effects of A1CF and AGO2 on testicular germ-cell tumors, testicular abnormalities, and fertilization bias.Proceedings of the National Academy of Sciences of the United States of America · 2016
    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

5 authors at 1 institution in 1 country.

Jason D HeaneyDepartment of Genetics, Case Comprehensive Cancer Center, Case Western Reserve University School of Medicine, Cleveland, OH 44120, USA. jason.heaney@case.edu
Megan V Michelson
Kirsten K Youngren
Man-Yee J Lam
Joseph H Nadeau
Case Western Reserve University · US

Funding

GENETIC CONTROL OF SUSCEPTIBILITY TO TESTICULAR CANCERR01CA075056 · NCI · PACIFIC NORTHWEST RESEARCH INSTITUTE · PI NADEAU, JOSEPH H. · 1998 to 2014
$5.7M
Testicular tumor susceptibility at the agouti locusF32CA119623 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI HEANEY, JASON D · 2006 to 2007
$95k
NCI NIH HHS CA119623NCI NIH HHS CA75056NCI NIH HHS F32 CA119623NCI NIH HHS R01 CA075056
6 · The paper itself

Abstract

The agouti-yellow (A(y)) deletion is the only genetic modifier known to suppress testicular germ cell tumor (TGCT) susceptibility in mice or humans. The A(y) mutation deletes Raly and Eif2s2, and induces the ectopic expression of agouti, all of which are potential TGCT-modifying mutations. Here we report that the reduced TGCT incidence of heterozygous A(y) males and the recessive embryonic lethality of A(y) are caused by the deletion of Eif2s2, the beta subunit of translation initiation factor eIF2. We found that the incidence of affected males was reduced 2-fold in mice that were partially deficient for Eif2s2 and that embryonic lethality occurred near the time of implantation in mice that were fully deficient for Eif2s2. In contrast, neither reduced expression of Raly in gene-trap mice nor ectopic expression of agouti in transgenic or viable-yellow (A(vy)) mutants affected TGCT incidence or embryonic viability. In addition, we provide evidence that partial deficiency of Eif2s2 attenuated germ cell proliferation and differentiation, both of which are important to TGCT formation. These results show that germ cell development and TGCT pathogenesis are sensitive to the availability of the eIF2 translation initiation complex and to changes in the rate of translation.

Indexed as

Genes, LethalAnimalsEukaryotic Initiation Factor-2Gene DeletionHomozygoteMaleMiceMice, TransgenicTesticular NeoplasmsTestisEukaryotic Initiation Factor-2

Identifiers

PMID19168544
PMCPMC2664146
OpenAlexW2147826510

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.