Evidence map›Paper›PMID 22253297›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2012

Common variation in Nemo-like kinase is associated with risk of ovarian cancer.

Kristen N Stevens, Linda E Kelemen, Xianshu Wang, Brooke L Fridley, Robert A Vierkant, Zachary Fredericksen, Sebastian M Armasu, Ya-Yu Tsai, Andrew Berchuck, Steven A Narod and 8 more

Open access · bronzeAbstract readComparative Study
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, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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

18 authors at 7 institutions in 2 countries.

Kristen N StevensDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota 55905, USA.
Linda E Kelemen
Xianshu Wang
Brooke L Fridley
Robert A Vierkant
Zachary Fredericksen
Sebastian M Armasu
Ya-Yu Tsai
Andrew Berchuck
Steven A Narod
Catherine M Phelan
Rebecca Sutphen
Michael J Birrer
Joellen M Schildkraut
Thomas A Sellers
Ellen L Goode
Ovarian Cancer Association Consortium
Fergus J Couch
Mayo Clinic · USWomen's College Hospital · CADuke Medical Center · USDuke University Hospital · USUniversity of South Florida · USAlberta Health Services · CABrigham and Women's Hospital · US

Funding

Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
Ovarian cancer GWAS discovery, expansion and replication (N2 - Project #1)U19CA148112 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI SELLERS, THOMAS A · 2010 to 2014
$10.2M
Mayo Cancer Genetic Epidemiology Training ProgramR25CA092049 · NCI · MAYO CLINIC ROCHESTER · PI PETERSEN, GLORIA M., VACHON, CELINE M · 2001 to 2018
$5.3M
A genome-wide association study for breast cancer in BRCA1 mutation carriersR01CA128978 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2008 to 2012
$4.8M
The Mitochondrial Genome and Ovarian Cancer RiskR01CA149429 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI PHELAN, CATHERINE · 2010 to 2015
$3.1M
Genetic epidemiology of cell division regulation in breast cancerR01CA122340 · NCI · MAYO CLINIC ROCHESTER · PI COUCH, FERGUS JOSEPH · 2007 to 2011
$3.0M
Population-Based Analysis of Ovarian Cancer BiomarkersR01CA106414 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI SUTPHEN, REBECCA · 2005 to 2009
$3.0M
Genetic Variation in the NF-kappaB Pathway and Ovarian Cancer EtiologyR01CA122443 · NCI · MAYO CLINIC ROCHESTER · PI GOODE, ELLEN L. · 2007 to 2012
$2.7M
Regulation of p53 function by DaxxR01CA088868 · NCI · UNIVERSITY OF PENNSYLVANIA · PI YANG, XIAOLU · 2001 to 2012
$2.6M
Estrogen Bioactivation and Risk of Ovarian CancerR01CA086888 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI SELLERS, THOMAS A · 2002 to 2005
$2.0M
NCI NIH HHS P50 CA136393NCI NIH HHS R01 CA086888NCI NIH HHS R01 CA088868NCI NIH HHS R01 CA106414NCI NIH HHS R01 CA122340NCI NIH HHS R01 CA122443NCI NIH HHS R01 CA128978NCI NIH HHS R01 CA149429NCI NIH HHS R01 CA88868NCI NIH HHS R25 CA092049NCI NIH HHS U19 CA148112
6 · The paper itself

Abstract

backgroundOverexpression of mitotic kinases has been associated with prognosis, histologic grade, and clinical stage in ovarian cancer, but the relationship between inherited variation in these genes and ovarian cancer risk has not been well defined.

methodsWe measured associations between 397 single nucleotide polymorphisms (SNPs) from 67 mitotic kinases and invasive epithelial ovarian cancer risk in two case-control studies (n = 671 cases; n = 939 controls). Thirty-six candidate SNPs (P < 0.05) were assessed in a replication analysis consisting of three additional studies (n = 1,094 cases; n = 829 controls).

resultsIn initial analysis, thirty-six SNPs were suggestive of association with risk of serous ovarian cancer, all subtypes of ovarian cancer, or both (P < 0.05). Replication analyses suggested an association between rs2125846 in the Nemo-like kinase (NLK) gene and ovarian cancer (serous OR = 1.36, 95% CI: 1.11-1.67, P = 1.77 × 10(-3); all subtypes OR = 1.30, 95% CI: 1.08-1.56, P = 2.97 × 10(-3)). Furthermore, rs2125846 was associated with risk in the combined discovery and replication sets (serous OR = 1.33, 95% CI: 1.15-1.54; all subtypes OR = 1.27, 95% CI: 1.12-1.45).

conclusionsVariation in NLK may be associated with risk of invasive epithelial ovarian cancer. Further studies are needed to confirm and understand the biologic relationship between this mitotic kinase and ovarian cancer risk. IMPACT: An association between SNPs in NLK and ovarian cancer may provide biologic insight into the development of this disease.

Indexed as

Biomarkers, TumorCase-Control StudiesCystadenocarcinoma, SerousDNA, NeoplasmFemaleFollow-Up StudiesHumansIntracellular Signaling Peptides and ProteinsMitosisNeoplasm InvasivenessOvarian NeoplasmsPolymerase Chain ReactionPolymorphism, Single NucleotidePrognosisProtein Serine-Threonine KinasesRisk FactorsBiomarkers, TumorDNA, NeoplasmIntracellular Signaling Peptides and ProteinsNLK protein, humanProtein Serine-Threonine Kinases

Identifiers

PMID22253297
PMCPMC3297683
OpenAlexW2150780897

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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.