Evidence map›Paper›PMID 16888336›Full record

ArticleGenetics2006

Zebrafish genomic instability mutants and cancer susceptibility.

Jessica L Moore, Lindsay M Rush, Carol Breneman, Manzoor-Ali P K Mohideen, Keith C Cheng

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Frontiers in oncology · 2017
    Review
  7. Article
  8. Review
  9. Current pathobiology reports · 2014
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Zebrafish models of germ cell tumor.Methods in cell biology · 2011
    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 3 institutions in 1 country.

Jessica L MooreThe Jake Gittlen Cancer Research Foundation, Department of Pathology, Pennsylvania State College of Medicine, Hershey, Pennsylvania 17033, USA.
Lindsay M Rush
Carol Breneman
Manzoor-Ali P K Mohideen
Keith C Cheng
Cancer Research Foundation · USHershey (United States) · USPenn State Milton S. Hershey Medical Center · US

Funding

Web-based Atlas of Zebrafish Microanatomy as a Community ResourceR24RR017441 · NCRR · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI CHENG, KEITH CHI · 2004 to 2011
$4.3M
A HISTOLOGIC SCREEN FOR CELL DIFFERENTIATION MUTANTSR01HD040179 · NICHD · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI CHENG, KEITH CHI · 2001 to 2005
$2.0M
VERTEBRATE MODEL OF DIFFERENTIATION/TUMOR SUPPRESSIONR01CA073935 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI CHENG, KEITH CHI · 1997 to 1999
–
NCI NIH HHS R01-CA73935NCRR NIH HHS R24 RR017441NICHD NIH HHS R01 HD040179NICHD NIH HHS R01-HD40179NIGMS NIH HHS F32-GM119794
6 · The paper itself

Abstract

Somatic loss of tumor suppressor gene function comprising the second hit of Knudson's two-hit hypothesis is important in human cancer. A genetic screen was performed in zebrafish (Danio rerio) to find mutations that cause genomic instability (gin), as scored by Streisinger's mosaic-eye assay that models this second hit. The assay, based on a visible test for loss of wild-type gene function at a single locus, golden, is representative of genomewide events. Twelve ENU-induced genomic instability (gin) mutations were isolated. Most mutations showed weak dominance in heterozygotes and all showed a stronger phenotype in homozygotes. Trans-heterozygosity for 7 of these mutations showed greatly enhanced instability. A variety of spontaneous tumors were found in heterozygous adults from all gin lines, consistent with the expectation that genomic instability (mutator) mutations can accelerate carcinogenesis. The incidence of spontaneous cancer at 30-34 months was increased 9.6-fold in heterozygotes for the mutant with the strongest phenotype, gin-10. Tumors were seen in skin, colon, kidney, liver, pancreas, ovary, testis, and neuronal tissues, with multiple tumors in some fish. The study of these mutants will add to our understanding of the mechanisms of somatic loss of gene function and how those mechanisms contribute to cancer susceptibility.

Indexed as

Genetic Predisposition to DiseaseGenomic InstabilityMutagenesisAnimalsFemaleMaleNeoplasmsPhenotypeZebrafish

Identifiers

PMID16888336
PMCPMC1602069
OpenAlexW2077786831

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.