Evidence map›Paper›PMID 24272484›Full record

ArticleCancer research2014

Risk of ovarian cancer and the NF-κB pathway: genetic association with IL1A and TNFSF10.

Bridget Charbonneau, Matthew S Block, William R Bamlet, Robert A Vierkant, Kimberly R Kalli, Zachary Fogarty, David N Rider, Thomas A Sellers, Shelley S Tworoger, Elizabeth Poole and 120 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 16% 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

32 citing papers in PubMed, 2 syntheses or guidelines pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. Common Polymorphisms in the NFKBIA Gene and Cancer Susceptibility: A Meta-Analysis.Medical science monitor : international medical journal of experimental and clinical research · 2015
    Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Associations betweenDisease markers · 2019
    Article
  19. Article
  20. 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

130 authors at 2 institutions in 2 countries.

Bridget CharbonneauAuthors' Affiliations: Departments of Health Sciences Research, Division of Epidemiology, Medical Oncology, Health Sciences Research, Division of Biomedical Statistics and Informatics, Immunology, and Laboratory Medicine and Pathology, Division of Experimental Pathology, Mayo Clinic, Rochester, Minnesota; Department of Cancer Epidemiology, Division of Population Sciences, Moffitt Cancer Center, Tampa, Florida; Channing Division of Network Medicine, Obstetrics and Gynecology Epidemiology Center, Brigham and Women's Hospital, Harvard Medical School; Department of Epidemiology, Harvard School of Public Health, Boston, Massachusetts; Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, Connecticut; Department of Clinical Science, University of Bergen; Departments of Gynecology and Obstetrics, and Pathology, Haukeland University Hospital, Bergen, Norway; Departments for Health Evidence, Urology, and Gynaecology, Radboud University Medical Centre, Nijmegen; Comprehensive Cancer Center The Netherlands, Utrecht, the Netherlands; Cancer Epidemiology Centre, The Cancer Council Victoria; Centre for Molecular, Environmental, Genetic and Analytical Epidemiology, Department of Pathology, and Sir Peter MacCallum Department of Oncology, University of Melbourne; Department of Epidemiology and Preventive Medicine, Monash University; Peter MacCallum Cancer Institute; Research Division, Peter MacCallum Cancer Centre, Melbourne, Victoria; Cancer Division, Queensland Institute of Medical Research, Herston, Queensland, Australia; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland; Department of Health Research and Policy, Division of Epidemiology, Stanford University School of Medicine, Palo Alto; Samuel Oschin Comprehensive Cancer Institute; Women's Cancer Program, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center; Department of Preventive Medicine, Keck School of Medicine, University of Sout
Matthew S Block
William R Bamlet
Robert A Vierkant
Kimberly R Kalli
Zachary Fogarty
David N Rider
Thomas A Sellers
Shelley S Tworoger
Elizabeth Poole
Harvey A Risch
Helga B Salvesen
Lambertus A Kiemeney
Laura Baglietto
Graham G Giles
Gianluca Severi
Britton Trabert
Nicolas Wentzensen
Georgia Chenevix-Trench
for AOCS/ACS group
Alice S Whittemore
Weiva Sieh
Jenny Chang-Claude
Elisa V Bandera
Irene Orlow
Kathryn Terry
Marc T Goodman
Pamela J Thompson
Linda S Cook
Mary Anne Rossing
Roberta B Ness
Steven A Narod
Jolanta Kupryjanczyk
Karen Lu
Ralf Butzow
Thilo Dörk
Tanja Pejovic
Ian Campbell
Nhu D Le
Clareann H Bunker
Natalia Bogdanova
Ingo B Runnebaum
Diana Eccles
James Paul
Anna H Wu
Simon A Gayther
Estrid Hogdall
Florian Heitz
Stanley B Kaye
Beth Y Karlan
Hoda Anton-Culver
Jacek Gronwald
Claus K Hogdall
Diether Lambrechts
Peter A Fasching
Usha Menon
Joellen Schildkraut
Celeste Leigh Pearce
Douglas A Levine
Susanne Kruger Kjaer
Daniel Cramer
James M Flanagan
Catherine M Phelan
Robert Brown
Leon F A G Massuger
Honglin Song
Jennifer A Doherty
Camilla Krakstad
Dong Liang
Kunle Odunsi
Andrew Berchuck
Allan Jensen
Jan Lubinski
Heli Nevanlinna
Yukie T Bean
Galina Lurie
Argyrios Ziogas
Christine Walsh
Evelyn Despierre
Louise Brinton
Alexander Hein
Anja Rudolph
Agnieszka Dansonka-Mieszkowska
Sara H Olson
Philipp Harter
Jonathan Tyrer
Allison F Vitonis
Angela Brooks-Wilson
Katja K Aben
Malcolm C Pike
Susan J Ramus
Elisabeth Wik
Cezary Cybulski
Jie Lin
Lara Sucheston
Robert Edwards
Valerie McGuire
Jenny Lester
Andreas du Bois
Lene Lundvall
Shan Wang-Gohrke
Lukasz M Szafron
Sandrina Lambrechts
Hannah Yang
Matthias W Beckmann
Liisa M Pelttari
Anne M Van Altena
David van den Berg
Mari K Halle
Aleksandra Gentry-Maharaj
Ira Schwaab
Urmila Chandran
Janusz Menkiszak
Arif B Ekici
Lynne R Wilkens
Arto Leminen
Francesmary Modugno
Grace Friel
Joseph H Rothstein
Ignace Vergote
Montserrat Garcia-Closas
Michelle A T Hildebrandt
Piotr Sobiczewski
Linda E Kelemen
Paul D P Pharoah
Kirsten Moysich
Keith L Knutson
Julie M Cunningham
Brooke L Fridley
Ellen L Goode
Moffitt Cancer Center · USRadboud University Nijmegen · NL

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
Hormone-Related CancersZIACP010126 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI GIERACH, GRETCHEN · 2009 to 2025
$103.5M
TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
University of Hawaii Cancer Center CCSGP30CA071789 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI Xin Chen · 1996 to 2026
$56.2M
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
Risk Factors for Breast Cancer in Younger NursesR01CA050385 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI ELIASSEN, A. HEATHER, WILLETT, WALTER C. · 1989 to 2019
$32.3M
WITHIN SUBJ VARIABILITY IN MEASUREMENTS DRUG METABOL ENZYMES IN HLTY SUBJM01RR000056 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEVINE, ARTHUR S · 1985 to 2006
$29.2M
Cancer Research UK 10124Cancer Research UK 13086Cancer Research UK 15960Cancer Research UK 16561Cancer Research UK C490/A10119Cancer Research UK C490/A10124Cancer Research UK C490/A6187Cancer Research UK C536/A13086Cancer Research UK C536/A6689CIHR MOP-86727CIHR MSH-87734NCI NIH HHS K07 CA080668NCI NIH HHS K07 CA092044NCI NIH HHS K07 CA095666NCI NIH HHS K07-CA095666NCI NIH HHS K07 CA143047NCI NIH HHS K07-CA143047NCI NIH HHS K07-CA80668NCI NIH HHS K22 CA138563NCI NIH HHS K22-CA138563NCI NIH HHS N01 CN025403NCI NIH HHS N01-CN55424NCI NIH HHS N01 PC035137NCI NIH HHS N01-PC035137NCI NIH HHS N01 PC067010NCI NIH HHS N01-PC067010NCI NIH HHS P01 CA017054NCI NIH HHS P01-CA017054NCI NIH HHS P01-CA087696NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA014089NCI NIH HHS P30 CA015083NCI NIH HHS P30 CA016056NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA071789NCI NIH HHS P30 CA072720NCI NIH HHS P30-CA072720NCI NIH HHS P30 CA076292NCI NIH HHS P50 CA105009NCI NIH HHS P50-CA105009NCI NIH HHS P50 CA136393NCI NIH HHS P50-CA136393NCI NIH HHS R01-CA014089NCI NIH HHS R01-CA016056NCI NIH HHS R01-CA017054NCI NIH HHS R01 CA049449NCI NIH HHS R01-CA049449NCI NIH HHS R01 CA050385NCI NIH HHS R01-CA050385NCI NIH HHS R01 CA054419NCI NIH HHS R01-CA054419NCI NIH HHS R01 CA058598NCI NIH HHS R01-CA058598NCI NIH HHS R01 CA058860NCI NIH HHS R01-CA058860NCI NIH HHS R01-CA061107NCI NIH HHS R01-CA061132NCI NIH HHS R01 CA063682NCI NIH HHS R01 CA064277NCI NIH HHS R01-CA064277NCI NIH HHS R01 CA067262NCI NIH HHS R01-CA067262NCI NIH HHS R01-CA071766NCI NIH HHS R01 CA074850NCI NIH HHS R01-CA074850NCI NIH HHS R01 CA076016NCI NIH HHS R01-CA076016NCI NIH HHS R01 CA080742NCI NIH HHS R01-CA080742NCI NIH HHS R01-CA080978NCI NIH HHS R01 CA083918NCI NIH HHS R01 CA087538NCI NIH HHS R01-CA087538NCI NIH HHS R01 CA087696NCI NIH HHS R01-CA092044NCI NIH HHS R01 CA106414NCI NIH HHS R01-CA106414NCI NIH HHS R01 CA112523NCI NIH HHS R01-CA112523NCI NIH HHS R01 CA114343NCI NIH HHS R01-CA114343NCI NIH HHS R01 CA122443NCI NIH HHS R01-CA122443NCI NIH HHS R01 CA126841NCI NIH HHS R01-CA126841NCI NIH HHS R01 CA128978NCI NIH HHS R01 CA149429NCI NIH HHS R01-CA149429NCI NIH HHS R03 CA113148NCI NIH HHS R03-CA113148NCI NIH HHS R03 CA115195NCI NIH HHS R03-CA115195NCI NIH HHS R25 CA092049NCI NIH HHS R25 CA92049NCI NIH HHS R37 CA070867NCI NIH HHS R37-CA070867NCI NIH HHS R37-CA70867NCI NIH HHS U01 CA069417NCI NIH HHS U01-CA069417NCI NIH HHS U01-CA071966NCI NIH HHS U19 CA148112NCI NIH HHS U19-CA148112NCI NIH HHS U19 CA148537NCI NIH HHS UM1 CA182910NCRR NIH HHS M01 RR000056NCRR NIH HHS MO1-RR000056Wellcome TrustWellcome Trust 076113
6 · The paper itself

Abstract

A missense single-nucleotide polymorphism (SNP) in the immune modulatory gene IL1A has been associated with ovarian cancer risk (rs17561). Although the exact mechanism through which this SNP alters risk of ovarian cancer is not clearly understood, rs17561 has also been associated with risk of endometriosis, an epidemiologic risk factor for ovarian cancer. Interleukin-1α (IL1A) is both regulated by and able to activate NF-κB, a transcription factor family that induces transcription of many proinflammatory genes and may be an important mediator in carcinogenesis. We therefore tagged SNPs in more than 200 genes in the NF-κB pathway for a total of 2,282 SNPs (including rs17561) for genotype analysis of 15,604 cases of ovarian cancer in patients of European descent, including 6,179 of high-grade serous (HGS), 2,100 endometrioid, 1,591 mucinous, 1,034 clear cell, and 1,016 low-grade serous, including 23,235 control cases spanning 40 studies in the Ovarian Cancer Association Consortium. In this large population, we confirmed the association between rs17561 and clear cell ovarian cancer [OR, 0.84; 95% confidence interval (CI), 0.76-0.93; P = 0.00075], which remained intact even after excluding participants in the prior study (OR, 0.85; 95% CI, 0.75-0.95; P = 0.006). Considering a multiple-testing-corrected significance threshold of P < 2.5 × 10(-5), only one other variant, the TNFSF10 SNP rs6785617, was associated significantly with a risk of ovarian cancer (low malignant potential tumors OR, 0.85; 95% CI, 0.79-0.91; P = 0.00002). Our results extend the evidence that borderline tumors may have a distinct genetic etiology. Further investigation of how these SNPs might modify ovarian cancer associations with other inflammation-related risk factors is warranted.

Indexed as

Signal TransductionCase-Control StudiesFemaleGenetic Association StudiesHumansInterleukin-1alphaNF-kappa BOvarian NeoplasmsPolymorphism, Single NucleotideRiskTNF-Related Apoptosis-Inducing LigandInterleukin-1alphaNF-kappa BTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, human

Identifiers

PMID24272484
PMCPMC3946482
OpenAlexW2139934419

What OpenQuestion holds

Textmetadata
LicenceTDM
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.