Evidence map›Paper›PMID 23472213›Full record

ArticlePloS one2013

The impact of 3'UTR variants on differential expression of candidate cancer susceptibility genes.

Laura E Skeeles, Jessica L Fleming, Kimberly L Mahler, Amanda Ewart Toland

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. 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
1.3field-weighted citation impact, top 20% 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, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Functional Analysis ofThe application of clinical genetics · 2024
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  4. Genetic polymorphisms of purinergic P2YPurinergic signalling · 2023
    Article
  5. Association ofInternational journal of molecular sciences · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Evaluating the Effect of 3'-UTR Variants inCurrent issues in molecular biology · 2021
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. A Quantitative Proteomics View on the Function ofPathogens (Basel, Switzerland) · 2018
    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

4 authors at 1 institution in 1 country.

Laura E SkeelesDepartment of Molecular Virology, Immunology and Medical Genetics, Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio, USA.
Jessica L Fleming
Kimberly L Mahler
Amanda Ewart Toland
The Ohio State University · US

Funding

Genetic interactions in colorectal cancer susceptibilityR01CA134461 · NCI · OHIO STATE UNIVERSITY · PI TOLAND, AMANDA EWART · 2010 to 2013
$1.2M
NCI NIH HHS CA134461NCI NIH HHS R01 CA134461
6 · The paper itself

Abstract

Variants in regulatory regions are predicted to play an important role in disease susceptibility of common diseases. Polymorphisms mapping to microRNA (miRNA) binding sites have been shown to disrupt the ability of miRNAs to target genes resulting in differential mRNA and protein expression. Skin tumor susceptibility 5 (Skts5) was identified as a locus conferring susceptibility to chemically-induced skin cancer in NIH/Ola by SPRET/Outbred F1 backcrosses. To determine if polymorphisms between the strains which mapped to putative miRNA binding sites in the 3' untranslated region (3'UTR) of genes at Skts5 influenced expression, we conducted a systematic evaluation of 3'UTRs of candidate genes across this locus. Nine genes had polymorphisms in their 3'UTRs which fit the linkage data and eight of these contained polymorphisms suspected to interfere with or introduce miRNA binding. 3'UTRs of six genes, Bcap29, Dgkb, Hbp1, Pik3cg, Twistnb, and Tspan13 differentially affected luciferase expression, but did not appear to be differentially regulated by the evaluated miRNAs predicted to bind to only one of the two isoforms. 3'UTRs from four additional genes chosen from the locus that fit less stringent criteria were evaluated. Ifrd1 and Etv1 showed differences and contained polymorphisms predicted to disrupt or create miRNA binding sites but showed no difference in regulation by the miRNAs tested. In summary, multiple 3'UTRs with putative functional variants between susceptible and resistant strains of mice influenced differential expression independent of predicted miRNA binding.

Indexed as

3' Untranslated RegionsGene Expression ProfilingGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseAnimalsBinding SitesCell LineCrosses, GeneticGenotypeMiceMicroRNAsMutagenesis, Site-DirectedNeoplasmsOncogenesPolymorphism, GeneticRNA, Messenger3' Untranslated RegionsMicroRNAsRNA, Messenger

Identifiers

PMID23472213
PMCPMC3589377
OpenAlexW2079513696

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.