Evidence map›Paper›PMID 29432432›Full record

ArticlePloS one2018

MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer.

Thomas Rohan, Kenny Ye, Yihong Wang, Andrew G Glass, Mindy Ginsberg, Olivier Loudig

Open access · goldAbstract readValidation Study
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 45% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Reference Genes for qPCR-Based miRNA Expression Profiling in 14 Human Tissues.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2022
    Review
  4. Article
  5. Article
  6. 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

6 authors at 4 institutions in 1 country.

Thomas RohanDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York, United States of America.ORCID 0000-0001-6897-4045
Kenny YeDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Yihong WangWarren Alpert Medical School of Brown University, Providence, Rhode Island, United States of America.
Andrew G GlassCenter for Health Research, Kaiser Permanente Northwest, Portland, Oregon, United States of America.
Mindy GinsbergDepartment of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York, United States of America.
Olivier LoudigHackensack University Medical Center, Hackensack, New Jersey, United States of America.
Albert Einstein College of Medicine · USBrown University · USHackensack University Medical Center · USKaiser Permanente Center for Health Research · US

Funding

Translational Research CoreP30DK020541 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STREAMSON C CHUA · 2015 to 2026
$27.7M
microRNA expression profiling of benign breast tissue and breast cancer riskR01CA142942 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI ROHAN, THOMAS E · 2010 to 2014
$3.6M
NCI NIH HHS R01 CA142942NIDDK NIH HHS P30 DK020541NIH HHS R01CA142942
6 · The paper itself

Abstract

MicroRNAs are endogenous, small non-coding RNAs that control gene expression by directing their target mRNAs for degradation and/or posttranscriptional repression. Abnormal expression of microRNAs is thought to contribute to the development and progression of cancer. A history of benign breast disease (BBD) is associated with increased risk of subsequent breast cancer. However, no large-scale study has examined the association between microRNA expression in BBD tissue and risk of subsequent invasive breast cancer (IBC). We conducted discovery and validation case-control studies nested in a cohort of 15,395 women diagnosed with BBD in a large health plan between 1971 and 2006 and followed to mid-2015. Cases were women with BBD who developed subsequent IBC; controls were matched 1:1 to cases on age, age at diagnosis of BBD, and duration of plan membership. The discovery stage (316 case-control pairs) entailed use of the Illumina MicroRNA Expression Profiling Assay (in duplicate) to identify breast cancer-associated microRNAs. MicroRNAs identified at this stage were ranked by the strength of the correlation between Illumina array and quantitative PCR results for 15 case-control pairs. The top ranked 14 microRNAs entered the validation stage (165 case-control pairs) which was conducted using quantitative PCR (in triplicate). In both stages, linear regression was used to evaluate the association between the mean expression level of each microRNA (response variable) and case-control status (independent variable); paired t-tests were also used in the validation stage. None of the 14 validation stage microRNAs was associated with breast cancer risk. The results of this study suggest that microRNA expression in benign breast tissue does not influence the risk of subsequent IBC.

Indexed as

BreastBreast NeoplasmsCohort StudiesFemaleHumansMicroRNAsNeoplasm InvasivenessReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionRisk FactorsMicroRNAs

Identifiers

PMID29432432
PMCPMC5809016
OpenAlexW2793844172

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.