Evidence map›Paper›PMID 27630279›Full record

ArticleAnticancer research2016

Mismatch Repair Polymorphisms as Markers of Breast Cancer Prevalence in the Breast Cancer Family Registry.

Maya Kappil, Mary Beth Terry, Lissette Delgado-Cruzata, Yuyan Liao, Regina M Santella

Open access · bronzeAbstract read
In one paragraph

Article in Anticancer research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 31 citations in OpenAlex.

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  11. Contribution ofFrontiers in oncology · 2018
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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

5 authors at 2 institutions in 1 country.

Maya KappilDepartment of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, U.S.A. maya.kappil@mssm.edu.
Mary Beth TerryDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, U.S.A. Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, U.S.A.
Lissette Delgado-CruzataDepartment of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, U.S.A.
Yuyan LiaoDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, U.S.A.
Regina M SantellaDepartment of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY, U.S.A. Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, U.S.A.
Columbia University · USColumbia University Irving Medical Center · US

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Parisa Tehranifar · 1985 to 2026
$115.3M
True Metal fac coreP30ES009089 · NIEHS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MATTHEW S PERZANOWSKI · 1998 to 2026
$44.7M
NCI NIH HHS P30 CA013696NIEHS NIH HHS P30 ES009089
6 · The paper itself

Abstract

backgroundMajor breast cancer susceptibility genes involved in DNA repair, including BRCA1 and BRCA2, have been identified. However, mutations in these genes account for only 5-10% of identified breast cancer cases. Additional DNA repair pathway genes may also contribute to susceptibility. MATERIALS AND

methodsWe investigated the association between 12 single nucleotide polymorphisms (SNPs) in mismatch repair (MMR) genes and breast cancer risk among 313 sister-sets enrolled in the New York site of the Breast Cancer Family Registry (BCFR) (n=744) using conditional logistic regression analysis.

resultsAn increase in breast cancer risk was observed for women with the MUTYH_rs3219489 variant allele (odds ratio (OR)=2.23, 95% confidence interval (CI)=1.10-4.52) and for women with the MSH2_rs2303428 variant allele (OR=1.73, 95% CI=1.00-2.99).

conclusionDeficiencies in DNA repair pathways, such as MMR, have implications for the onset of familial breast cancer.

Indexed as

DNA Mismatch RepairPolymorphism, Single NucleotideAdultAllelesBreast NeoplasmsCase-Control StudiesColorectal Neoplasms, Hereditary NonpolyposisDNA RepairExonsFamily HealthFemaleGenes, BRCA1Genes, BRCA2GenotypeHeterozygoteHumansBreast cancerfamily historymismatch repairsingle nucleotide polymorphisms

Identifiers

PMID27630279
PMCPMC5278884
OpenAlexW2513667126

What OpenQuestion holds

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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.