Evidence map›Paper›PMID 23462292›Full record

SynthesisHuman molecular genetics2013

Testicular germ cell tumor susceptibility associated with the UCK2 locus on chromosome 1q23.

Fredrick R Schumacher, Zhaoming Wang, Rolf I Skotheim, Roelof Koster, Charles C Chung, Michelle A T Hildebrandt, Christian P Kratz, Anne C Bakken, D Timothy Bishop, Michael B Cook and 25 more

Registry-linked trialOpen access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in Human molecular genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00034424 (Multidisciplinary Etiologic Study of Familial Testicular Cancer), which is not on this map. Cited by 45 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 8 pooled it
9.6field-weighted citation impact, top 1% 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.

NCT00034424 completednot on this map

Multidisciplinary Etiologic Study of Familial Testicular Cancer

TypeobservationalSponsorNational Cancer Institute (NCI)Ran2003Enrolled749ConditionsTesticular Cancer
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 8 syntheses or guidelines pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Association Study between Polymorphisms in DNA Methylation-Related Genes and Testicular Germ Cell Tumor Risk.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022
    Pooled it
  3. Pooled it
  4. TERT rs10069690 polymorphism and cancers risk: A meta-analysis.Molecular genetics & genomic medicine · 2019
    Pooled it
  5. Pooled it
  6. Pooled it
  7. Pooled it
  8. Pooled it
  9. Article
  10. Article
  11. Article
  12. Review
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  14. Review
  15. Article
  16. Increasing Incidence of Testicular Germ Cell Tumors among Racial/Ethnic Minorities in the United States.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020
    Article
  17. Article
  18. Article
  19. Article
  20. Testicular germ cell tumor: a comprehensive review.Cellular and molecular life sciences : CMLS · 2019
    Review
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

35 authors at 19 institutions in 4 countries.

Fredrick R SchumacherDepartment of Preventive Medicine, Keck School of Medicine, University of Southern California/Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
Zhaoming Wang
Rolf I Skotheim
Roelof Koster
Charles C Chung
Michelle A T Hildebrandt
Christian P Kratz
Anne C Bakken
D Timothy Bishop
Michael B Cook
R Loren Erickson
Sophie D Fosså
Mark H Greene
Kevin B Jacobs
Peter A Kanetsky
Laurence N Kolonel
Jennifer T Loud
Larissa A Korde
Loic Le Marchand
Juan Pablo Lewinger
Ragnhild A Lothe
Malcolm C Pike
Nazneen Rahman
Mark V Rubertone
Stephen M Schwartz
Kimberly D Siegmund
Eila C Skinner
Clare Turnbull
David J Van Den Berg
Xifeng Wu
Meredith Yeager
Katherine L Nathanson
Stephen J Chanock
Victoria K Cortessis
Katherine A McGlynn
National Cancer Institute · USUniversity of Southern California · USOslo University Hospital · NOInstitute of Cancer Research · GBThe University of Texas MD Anderson Cancer Center · USCancer Center of Hawaii · USDivision of Cancer Epidemiology and GeneticsFred Hutch Cancer Center · USMedizinische Hochschule Hannover · DEMemorial Sloan Kettering Cancer Center · USNational Institutes of Health · USStanford University · USSt James's University Hospital · GBUniversity of Hawaii System · USUniversity of Oslo · NOUniversity of Pennsylvania · USUniversity of Washington · USU.S. Army Center for Health Promotion and Preventive Medicine · USWalter Reed Army Institute of Research · US

Funding

Clinical Genetic Studies of Familial and Hereditary Cancer SyndromesZIACP010144 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI SAVAGE, SHARON A. · 2009 to 2025
$111.8M
Characterizing Genetic Susceptibility to Breast and Prostate Cancer; the BPC3U01CA098758 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HENDERSON, BRIAN E · 2003 to 2010
$11.0M
MOLECULAR EPIDEMIOLOGY OF TESTICULAR CARCINOMAR01CA085914 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SCHWARTZ, STEPHEN M · 2000 to 2009
$8.4M
A Genetic Linkage Study of Testicular CancerR01CA102042 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CORTESSIS, VICTORIA K · 2004 to 2009
$3.9M
Inherited genetic variation and predisposition to testicular germ cell tumorR01CA114478 · NCI · UNIVERSITY OF PENNSYLVANIA · PI NATHANSON, KATHERINE L. · 2007 to 2011
$3.1M
Cancer Research UK 10589Intramural NIH HHSNCI NIH HHS 1R01 CA102042-01A1NCI NIH HHS NCI U01-CA98758NCI NIH HHS R01 CA085914NCI NIH HHS R01CA085914NCI NIH HHS R01 CA102042NCI NIH HHS R01 CA114478NCI NIH HHS R01CA114478NCI NIH HHS U01 CA098758
6 · The paper itself

Abstract

Genome-wide association studies (GWASs) have identified multiple common genetic variants associated with an increased risk of testicular germ cell tumors (TGCTs). A previous GWAS reported a possible TGCT susceptibility locus on chromosome 1q23 in the UCK2 gene, but failed to reach genome-wide significance following replication. We interrogated this region by conducting a meta-analysis of two independent GWASs including a total of 940 TGCT cases and 1559 controls for 122 single-nucleotide polymorphisms (SNPs) on chromosome 1q23 and followed up the most significant SNPs in an additional 2202 TGCT cases and 2386 controls from four case-control studies. We observed genome-wide significant associations for several UCK2 markers, the most significant of which was for rs3790665 (PCombined = 6.0 × 10(-9)). Additional support is provided from an independent familial study of TGCT where a significant over-transmission for rs3790665 with TGCT risk was observed (PFBAT = 2.3 × 10(-3)). Here, we provide substantial evidence for the association between UCK2 genetic variation and TGCT risk.

Indexed as

Chromosomes, Human, Pair 1Genetic LociGenetic Predisposition to DiseaseCase-Control StudiesGenotypeHumansLinkage DisequilibriumMaleNeoplasms, Germ Cell and EmbryonalPolymorphism, Single NucleotideRecombination, GeneticTesticular NeoplasmsUridine KinaseUCK2 protein, humanUridine Kinase

Identifiers

PMID23462292
PMCPMC3674801
OpenAlexW2115003624

What OpenQuestion holds

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Registered trials

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.