Evidence map›Paper›PMID 25410285›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2014

Interactions between ultraviolet light and MC1R and OCA2 variants are determinants of childhood nevus and freckle phenotypes.

Anna E Barón, Nancy L Asdigian, Victoria Gonzalez, Jenny Aalborg, Tamara Terzian, Regan A Stiegmann, Enrique C Torchia, Marianne Berwick, Robert P Dellavalle, Joseph G Morelli and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. ModulatingBiomolecules · 2024
    Article
  3. Review
  4. The Metabolite Profile in Culture Supernatant ofPlants (Basel, Switzerland) · 2021
    Article
  5. MC1R variants in relation to naevi in melanoma cases and controls: a pooled analysis from the M-SKIP project.Journal of the European Academy of Dermatology and Venereology : JEADV · 2021
    Article
  6. Review
  7. Article
  8. Cutaneous nevi and risk of melanoma death in women and men: A prospective study.Journal of the American Academy of Dermatology · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. 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

13 authors at 1 institution in 1 country.

Anna E BarónDepartment of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Nancy L AsdigianDepartment of Community and Behavioral Health, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Victoria GonzalezDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado. Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Jenny AalborgDepartment of Community and Behavioral Health, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Tamara TerzianDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado. Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Regan A StiegmannDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado. Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Enrique C TorchiaDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado. Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Marianne BerwickDivision of Epidemiology, University of New Mexico, Albuquerque, New Mexico.
Robert P DellavalleDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado. Dermatology Service, Department of Veterans Affairs, Eastern Colorado Health Care System, Denver, Colorado. Department of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Joseph G MorelliDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Stefan T MokrohiskyKaiser Permanente Health Plan of Colorado, Denver, Colorado.
Lori A CraneDepartment of Community and Behavioral Health, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Neil F BoxDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado. Charles C. Gates Center for Regenerative Medicine and Stem Cell Biology, University of Colorado Anschutz Medical Campus, Aurora, Colorado. neil.box@ucdenver.edu.
University of Colorado Anschutz Medical Campus · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Transgenic and Gene Targeting CoreP30AR057212 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI HOGAN, CHRISTOPHER J · 2009 to 2018
$6.2M
SKIN CANCER PREVENTION IN A PEDIATRIC POPULATIONR01CA074592 · NCI · UNIVERSITY OF COLORADO DENVER · PI BOX, NEIL FREDERICK, CRANE, LORI A. · 1997 to 2014
$5.2M
Melanoma Prevention: Using the SunK05CA131675 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BERWICK, MARIANNE · 2011 to 2015
$795k
Targeting p53-Dependent Repigmentation in VitiligoK01AR063203 · NIAMS · UNIVERSITY OF COLORADO DENVER · PI TERZIAN, TAMARA G · 2012 to 2016
$503k
NCATS NIH HHS UL1 TR001082NCI NIH HHS 5R01CA74592NCI NIH HHS K05 CA131675NCI NIH HHS P30 CA046934NCI NIH HHS P30CA046934NCI NIH HHS R01 CA074592NCRR NIH HHS UL1 RR025780NCRR NIH HHS UL1RR025780NIAMS NIH HHS K01 AR063203NIAMS NIH HHS P30 AR057212
6 · The paper itself

Abstract

backgroundMelanocytic nevi (moles) and freckles are well known biomarkers of melanoma risk, and they are influenced by similar UV light exposures and genetic susceptibilities to those that increase melanoma risk. Nevertheless, the selective interactions between UV exposures and nevus and freckling genes remain largely undescribed.

methodsWe conducted a longitudinal study from ages 6 through 10 years in 477 Colorado children who had annual information collected for sun exposure, sun protection behaviors, and full body skin exams. MC1R and HERC2/OCA2 rs12913832 were genotyped and linear mixed models were used to identify main and interaction effects.

resultsAll measures of sun exposure (chronic, sunburns, and waterside vacations) contributed to total nevus counts, and cumulative chronic exposure acted as the major driver of nevus development. Waterside vacations strongly increased total nevus counts in children with rs12913832 blue eye color alleles and facial freckling scores in those with MC1R red hair color variants. Sunburns increased the numbers of larger nevi (≥2 mm) in subjects with certain MC1R and rs12913832 genotypes.

conclusionsComplex interactions between different UV exposure profiles and genotype combinations determine nevus numbers and size, and the degree of facial freckling. IMPACT: Our findings emphasize the importance of implementing sun-protective behavior in childhood regardless of genetic make-up, although children with particular genetic variants may benefit from specifically targeted preventive measures to counteract their inherent risk of melanoma. Moreover, we demonstrate, for the first time, that longitudinal studies are a highly powered tool to uncover new gene-environment interactions that increase cancer risk.

Indexed as

Albinism, OculocutaneousChildCohort StudiesFemaleGenotypeHumansMaleMelanosisNevus, PigmentedPhenotypeReceptor, Melanocortin, Type 1Ultraviolet RaysReceptor, Melanocortin, Type 1

Identifiers

PMID25410285
PMCPMC4257874
OpenAlexW2044096549

What OpenQuestion holds

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Registered trials

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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.