Evidence map›Paper›PMID 21764761›Full record

ArticleCancer research2011

Identification of fat4 and tsc22d1 as novel candidate genes for spontaneous pulmonary adenomas.

Annerose Berndt, Clinton L Cario, Kathleen A Silva, Victoria E Kennedy, David E Harrison, Beverly Paigen, John P Sundberg

Abstract read
In one paragraph

Article in Cancer research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Mouse genome-wide association study identifies polymorphisms on chromosomes 4, 11, and 15 for age-related cardiac fibrosis.Mammalian genome : official journal of the International Mammalian Genome Society · 2016
    Article
  14. Article
  15. Article
  16. Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span.The journals of gerontology. Series A, Biological sciences and medical sciences · 2016
    Article
  17. Article
  18. Article
  19. Review
  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

7 authors at 2 institutions in 1 country.

Annerose BerndtBerndt Laboratory, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA. anb128@pitt.edu
Clinton L Cario
Kathleen A Silva
Victoria E Kennedy
David E Harrison
Beverly Paigen
John P Sundberg
University of Pittsburgh · USJackson Laboratory · US

Funding

Mouse Models of Human Cancer DatabaseR01CA089713 · NCI · JACKSON LABORATORY · PI BULT, CAROL J · 2002 to 2025
$17.5M
Shock Center for Aging Research at The Jackson Laborato*P30AG025707 · NIA · JACKSON LABORATORY · PI PAIGEN, BEVERLY J · 2005 to 2009
$4.1M
Lifespan Extension Despite Greatly Elevated Insulin and Body FatR01AG032333 · NIA · JACKSON LABORATORY · PI HARRISON, DAVID E · 2010 to 2014
$1.8M
NCI NIH HHS CA89713NCI NIH HHS R01 CA089713NIA NIH HHS AG25707NIA NIH HHS P30 AG025707NIA NIH HHS R01 AG032333
6 · The paper itself

Abstract

Genetic influences that underlie spontaneous lung oncogenesis are poorly understood. The objective of this study was to determine the genetic influences on spontaneous pulmonary adenoma frequency and severity in 28 strains of mice as part of a large-scale aging study conducted at the Jackson Aging Center (http://agingmice.jax.org/). Genome-wide association studies were conducted in these strains with both low-density (132,000) and high-density (4,000,000) panel of single-nucleotide polymorphisms (SNP). Our analysis revealed that adenomas were relatively less frequent and less severe in females than males, and that loci implicated in frequency and severity were often different between male and female mice. While some of the significant loci identified mapped to genomic locations known to be responsible for carcinogen-induced cancers (e.g., Pas1), others were unique to our study. In particular, Fat4 was influential in males and Tsc22d1 was influential in females. SNPs implicated were predicted to alter amino acid sequence and change protein function. In summary, our results suggested that genetic influences that underlie pulmonary adenoma frequency are dependent on gender, and that Fat4 and Tsc22d1 are likely candidate genes to influence formation of spontaneous pulmonary adenoma in aging male and female mice, respectively.

Indexed as

AdenomaAge FactorsAgingAnimalsCadherinsFemaleGenetic LociGenome-Wide Association StudyLung NeoplasmsMaleMiceMice, Inbred StrainsRepressor ProteinsSeverity of Illness IndexCadherinsFat4 protein, mouseRepressor ProteinsTgfb1i4 protein, mouse

Identifiers

PMID21764761
PMCPMC3165088
OpenAlexW2167780877

What OpenQuestion holds

Textmetadata
LicenceTDM
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.