Evidence map›Paper›PMID 24062209›Full record

ArticleBreast cancer research and treatment2013

Genetic variants in microRNAs and breast cancer risk in African American and European American women.

Song Yao, Kelly Graham, Jie Shen, Lara E Sucheston Campbell, Prashant Singh, Gary Zirpoli, Michelle Roberts, Gregory Ciupak, Warren Davis, Helena Hwang and 8 more

Open access · greenAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 19% 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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 41 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 6 institutions in 1 country.

Song YaoDepartment of Cancer Prevention & Control, Roswell Park Cancer Institute, Buffalo, NY, USA, song.yao@roswellpark.org.
Kelly Graham
Jie Shen
Lara E Sucheston Campbell
Prashant Singh
Gary Zirpoli
Michelle Roberts
Gregory Ciupak
Warren Davis
Helena Hwang
Thaer Khoury
Dana H Bovbjerg
Lina Jandorf
Karen S Pawlish
Elisa V Bandera
Song Liu
Christine B Ambrosone
Hua Zhao
Roswell Park Comprehensive Cancer Center · USThe University of Texas MD Anderson Cancer Center · USIcahn School of Medicine at Mount Sinai · USNew Jersey Department of Health · USRutgers Cancer Institute of New JerseyUniversity of Pittsburgh · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
Race &Risk Factors for Early/Aggressive Breast CancerR01CA100598 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI AMBROSONE, CHRISTINE B. · 2004 to 2008
$4.8M
Epidemiologic and Basic Science in Cancer PreventionR25CA114101 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARSHALL, JAMES · 2006 to 2010
$2.3M
MIcroRNA: A Novel Genetic Modifier for Breast Cancer PredispositionR01CA136483 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ZHAO, HUA · 2009 to 2012
$2.2M
NCCDPHP CDC HHS 1U58DP00039311-01NCI NIH HHS N01-PC-2010-00027NCI NIH HHS P30 CA016056NCI NIH HHS P30 CA016056-32NCI NIH HHS R01 CA100598NCI NIH HHS R01 CA136483NCI NIH HHS R25 CA114101
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are an integral part of the post-transcriptional machinery of gene expression and have been implicated in the carcinogenic cascade. Single nucleotide polymorphisms (SNPs) in miRNAs and risk of breast cancer have been evaluated in populations of European or Asian ancestry, but not among women of African ancestry. Here we examined 145 SNPs in six miRNA processing genes and in 78 miRNAs which target genes known to be important in breast cancer among 906 African American (AA) and 653 European American (EA) cases and controls enrolled in the Women's Circle of Health Study. Allele frequencies of most SNPs (87 %) differed significantly by race. We found a number of SNPs in miRNAs and processing genes in association with breast cancer overall or stratified by estrogen receptor (ER) status. Several associations were significantly different by race, with none of the associations being significant in both races. Using a polygenic risk score to combine the effects of multiple SNPs, we found significant associations with the score in each subgroup analysis. For ER-positive cancer, each unit increment of the risk score was associated with a 51 % increased risk in AAs (OR = 1.51, 95 % CI = 1.30-1.74, p = 3.3 × 10(-8)) and a 73 % increased risk in EAs (OR = 1.73, 95 % CI = 1.45-2.06, p = 1.4 × 10(-9)). These data show, for the first time, that miRNA-related genetic variations may underlie the etiology of breast cancer in both populations of African and European ancestries. Future studies are needed to validate our findings and to explore the underlying mechanisms.

Indexed as

Polymorphism, Single NucleotideAdultBlack or African AmericanBreast NeoplasmsFemaleGene FrequencyGenetic Association StudiesHumansLinkage DisequilibriumMicroRNAsMiddle AgedReceptors, EstrogenRiskWhite PeopleMicroRNAsReceptors, Estrogen

Identifiers

PMID24062209
PMCPMC3856568
OpenAlexW2056267055

What OpenQuestion holds

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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.