Evidence map›Paper›PMID 22581838›Full record

ArticleCarcinogenesis2012

A population-based study of DNA repair gene variants in relation to non-melanoma skin cancer as a marker of a cancer-prone phenotype.

Ingo Ruczinski, Timothy J Jorgensen, Yin Yao Shugart, Yvette Berthier Schaad, Bailey Kessing, Judith Hoffman-Bolton, Kathy J Helzlsouer, W H Linda Kao, Lee Wheless, Lesley Francis and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-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

16 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. 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

14 authors at 8 institutions in 1 country.

Ingo RuczinskiDepartment of Biostatistics, The Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.
Timothy J Jorgensen
Yin Yao Shugart
Yvette Berthier Schaad
Bailey Kessing
Judith Hoffman-Bolton
Kathy J Helzlsouer
W H Linda Kao
Lee Wheless
Lesley Francis
Rhoda M Alani
Paul T Strickland
Michael W Smith
Anthony J Alberg
Johns Hopkins University · USMedical University of South Carolina · USScience Applications International Corporation (United States) · USZero to Three · USBoston University · USMercy Medical Center · USMUSC Hollings Cancer Center · USNational Institute of Mental Health · US

Funding

Developing new statisical methods to detect variants involved in complex diseaseZIAMH002929 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI YAO, YIN · 2011 to 2016
$2.6M
DNA Repair, Skin Cancer and Overall Cancer RiskR01CA105069 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI ALBERG, ANTHONY J · 2005 to 2009
$2.4M
Developing Stats Methods to Detect Rare Genetics Variants in Human PedigreesZIAMH002930 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI YAO, YIN · 2011 to 2016
$1.6M
Intramural NIH HHSNCI NIH HHS R01 CA105069PHS HHS HHSN26120080001E
6 · The paper itself

Abstract

For unknown reasons, non-melanoma skin cancer (NMSC) is associated with increased risk of other malignancies. Focusing solely on DNA repair or DNA repair-related genes, this study tested the hypothesis that DNA repair gene variants contribute to the increased cancer risk associated with a personal history of NMSC. From the parent CLUE II cohort study, established in 1989 in Washington County, MD, the study consisted of a cancer-free control group (n 5 2296) compared with three mutually exclusive groups of cancer cases ascertained through 2007: (i) Other (non-NMSC) cancer only (n 5 2349); (ii) NMSC only (n 5 694) and (iii) NMSC plus other cancer (n 5 577). The frequency of minor alleles in 759 DNA repair gene single nucleotide polymorphisms (SNPs) was compared in these four groups. Comparing those with both NMSC and other cancer versus those with no cancer, 10 SNPs had allelic trend P-values <0.01. The two top-ranked SNPs were both within the thymine DNA glycosylase gene (TDG). One was a non-synonymous coding SNP (rs2888805) [per allele odds ratio (OR) 1.40, 95% confidence interval (CI) 1.16-1.70; P-value 5 0.0006] and the other was an intronic SNP in high linkage disequilibrium with rs2888805 (rs4135150). None of the associations had a P-value <6.6310(-5), the threshold for statistical significance after correcting for multiple comparisons. The results pinpoint DNA repair genes most likely to contribute to the NMSC cancer-prone phenotype. A promising lead is genetic variants in TDG, important not only in base excision repair but also in regulating the epigenome and gene expression, which may contribute to the NMSC-associated increase in overall cancer risk.

Indexed as

Polymorphism, Single NucleotideAdultAgedBiomarkers, TumorDNA-Binding ProteinsDNA HelicasesDNA RepairFemaleHumansMaleMiddle AgedPhenotypeSkin NeoplasmsThymine DNA GlycosylaseBiomarkers, TumorDNA-Binding ProteinsDNA HelicasesThymine DNA GlycosylaseXPBC-ERCC-3 protein

Identifiers

PMID22581838
PMCPMC3514896
OpenAlexW2105559847

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.