Evidence map›Paper›PMID 29425227›Full record

SynthesisPloS one2018

Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations.

Harsh Sheth, Emma Northwood, Cornelia M Ulrich, Dominique Scherer, Faye Elliott, Jennifer H Barrett, David Forman, C Roland Wolf, Gillian Smith, Michael S Jackson and 12 more

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

Synthesis in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02328677 (ColoCare Transdisciplinary Research in Colorectal Cancer Prognosis), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
4.1field-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.

NCT02328677 recruitingnot on this map

ColoCare Transdisciplinary Research in Colorectal Cancer Prognosis

TypeobservationalSponsorUniversity of UtahRan2007 to 2030Enrolled5,000ConditionsColorectal Cancer
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 32 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

22 authors at 12 institutions in 5 countries.

Harsh ShethInstitute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.ORCID 0000-0001-9626-0971
Emma NorthwoodLeeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom.
Cornelia M UlrichHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah, United States of America.
Dominique SchererInstitute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.
Faye ElliottLeeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom.
Jennifer H BarrettLeeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom.
David FormanLeeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom.
C Roland WolfSchool of Medicine, University of Dundee, Dundee, United Kingdom.
Gillian SmithSchool of Medicine, University of Dundee, Dundee, United Kingdom.
Michael S JacksonInstitute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Mauro Santibanez-KorefInstitute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Robert HaileStanford Cancer Institute, Stanford, California, United States of America.
Graham CaseyCenter for Public Health Genomics, University of Virginia, Charlottesville, Virginia, United States of America.
Mark JenkinsMelbourne School of Population and Global Health, The University of Melbourne, Carlton, Australia.
Aung Ko WinMelbourne School of Population and Global Health, The University of Melbourne, Carlton, Australia.
John L HopperMelbourne School of Population and Global Health, The University of Melbourne, Carlton, Australia.
Loic Le MarchandUniversity of Hawaii, Manoa, Hawaii, United States of America.
Noralane M LindorMayo Clinic, Scottsdale, Arizona, United States of America.
Stephen N ThibodeauMayo Clinic, Rochester, Minnesota, United States of America.
John D PotterCentre for Public Health Research, Massey University, Wellington, New Zealand.
John BurnInstitute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
D Timothy BishopLeeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom.
University of Leeds · GBNewcastle University · GBThe University of Melbourne · AUUniversity of Dundee · GBCancer Prevention Institute of California · USHeidelberg University · DEMassey University · NZMayo Clinic · USMayo Clinic in Arizona · USUniversity of Hawaiʻi at Mānoa · USUniversity of Utah · USUniversity of Virginia · US

Funding

SEATTLE FAMILIAL COLORECTAL CANCER REGISTRYU01CA074794 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWCOMB, POLLY A · 1997 to 2007
$14.1M
ONTARIO REGISTRY FOR STUDIES OF FAMILIAL COLON CANCERU01CA074783 · NCI · CANCER CARE ONTARIO · PI GALLINGER, STEVEN · 1997 to 2008
$12.5M
Colon Cancer Family Registry CohortUM1CA167551 · NCI · STANFORD UNIVERSITY · PI HAILE, ROBERT WILLIAM, JENKINS, MARK A · 2013 to 2017
$11.3M
Inherited colorectal cancer risk variants: from association to biologyR01CA143237 · NCI · UNIVERSITY OF VIRGINIA · PI CASEY, GRAHAM · 2010 to 2020
$8.4M
Genomic Wide Association Study of Colorectal CancerU01CA122839 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CASEY, GRAHAM · 2006 to 2010
$7.3M
The Colon Cancer Family Registry: SeattleU24CA074794 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NEWCOMB, POLLY A · 2008 to 2011
$7.0M
AUSTRALASIAN COLORECTAL CANCER FAMILY REGISTRYU01CA097735 · NCI · UNIVERSITY OF MELBOURNE · PI HOPPER, JOHN L · 2002 to 2007
$6.9M
The Colon Cancer Family Registry: AustralasiaU24CA097735 · NCI · UNIVERSITY OF MELBOURNE · PI HOPPER, JOHN L · 2008 to 2011
$6.2M
Discovery and verification of novel biomarkers of colorectal cancer recurrenceR01CA189184 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LI, CHRISTOPHER I, ULRICH, CORNELIA M · 2015 to 2020
$5.6M
The Colon Cancer Family Registry: OntarioU24CA074783 · NCI · CANCER CARE ONTARIO · PI GALLINGER, STEVEN · 2008 to 2011
$4.1M
Metabolomic Strategies for Discovery and Validation of Biomarkers of Colorectal Cancer RecurrenceR01CA207371 · NCI · UNIVERSITY OF UTAH · PI LI, CHRISTOPHER I, ULRICH, CORNELIA M · 2017 to 2022
$3.9M
AUSTRALASIAN C0L0RECTAL CANCER FAMILY STUDYU01CA074778 · NCI · UNIVERSITY OF QUEENSLAND · PI JASS, JEREMY R · 1997 to 2002
$1.3M
Cancer Research UK 10589Cancer Research UK 10822Cancer Research UK 15934Cancer Research UK 19167Cancer Research UK 22357NCI NIH HHS R01 CA143237NCI NIH HHS R01 CA189184NCI NIH HHS R01 CA207371NCI NIH HHS U01 CA074783NCI NIH HHS U01 CA074794NCI NIH HHS U01 CA097735NCI NIH HHS U01 CA122839NCI NIH HHS U24 CA074783NCI NIH HHS U24 CA074794NCI NIH HHS U24 CA097735NCI NIH HHS UM1 CA167551NIH HHS R01 CA143237NIH HHS U01 CA074778NIH HHS U01 CA122839NIH HHS U01/U24 CA074783NIH HHS U01/U24 CA074794NIH HHS U01/U24 CA097735NIH HHS UM1 CA167551
6 · The paper itself

Abstract

Regular aspirin use is associated with reduced risk of colorectal cancer (CRC). Variation in aspirin's chemoprevention efficacy has been attributed to the presence of single nucleotide polymorphisms (SNPs). We conducted a meta-analysis using two large population-based case-control datasets, the UK-Leeds Colorectal Cancer Study Group and the NIH-Colon Cancer Family Registry, having a combined total of 3325 cases and 2262 controls. The aim was to assess 42 candidate SNPs in 15 genes whose association with colorectal cancer risk was putatively modified by aspirin use, in the literature. Log odds ratios (ORs) and standard errors were estimated for each dataset separately using logistic regression adjusting for age, sex and study site, and dataset-specific results were combined using random effects meta-analysis. Meta-analysis showed association between SNPs rs6983267, rs11694911 and rs2302615 with CRC risk reduction (All P<0.05). Association for SNP rs6983267 in the CCAT2 gene only was noteworthy after multiple test correction (P = 0.001). Site-specific analysis showed association between SNPs rs1799853 and rs2302615 with reduced colon cancer risk only (P = 0.01 and P = 0.004, respectively), however neither reached significance threshold following multiple test correction. Meta-analysis of SNPs rs2070959 and rs1105879 in UGT1A6 gene showed interaction between aspirin use and CRC risk (Pinteraction = 0.01 and 0.02, respectively); stratification by aspirin use showed an association for decreased CRC risk for aspirin users having a wild-type genotype (rs2070959 OR = 0.77, 95% CI = 0.68-0.86; rs1105879 OR = 0.77 95% CI = 0.69-0.86) compared to variant allele cariers. The direction of the interaction however is in contrast to that published in studies on colorectal adenomas. Both SNPs showed potential site-specific interaction with aspirin use and colon cancer risk only (Pinteraction = 0.006 and 0.008, respectively), with the direction of association similar to that observed for CRC. Additionally, they showed interaction between any non-steroidal anti-inflammatory drugs (including aspirin) use and CRC risk (Pinteraction = 0.01 for both). All gene x environment (GxE) interactions however were not significant after multiple test correction. Candidate gene investigation indicated no evidence of GxE interaction between genetic variants in genes involved in aspirin pathways, regular aspirin use and colorectal cancer risk.

Indexed as

Polymorphism, Single NucleotideWhite PeopleAspirinAustraliaCanadaCase-Control StudiesColorectal NeoplasmsHumansRisk FactorsUnited StatesAspirin

Identifiers

PMID29425227
PMCPMC5806861
OpenAlexW2787448435

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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.