Evidence map›Paper›PMID 25440114›Full record

ArticleThe American journal of pathology2014

Stromal expression of miR-21 identifies high-risk group in triple-negative breast cancer.

Todd A MacKenzie, Gary N Schwartz, Heather M Calderone, Carrie R Graveel, Mary E Winn, Galen Hostetter, Wendy A Wells, Lorenzo F Sempere

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 3 pooled it
2.5field-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

41 citing papers in PubMed, 3 syntheses or guidelines pooled it, 56 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

8 authors at 2 institutions in 1 country.

Todd A MacKenzieDepartment of Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Gary N SchwartzDepartment of Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Heather M CalderoneCenter for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, Michigan.
Carrie R GraveelCenter for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, Michigan.
Mary E WinnBioinformatics and Biostatistics Core, Van Andel Research Institute, Grand Rapids, Michigan.
Galen HostetterLaboratory of Analytical Pathology, Van Andel Research Institute, Grand Rapids, Michigan.
Wendy A WellsDepartment of Pathology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Lorenzo F SempereCenter for Cancer and Cell Biology, Van Andel Research Institute, Grand Rapids, Michigan; Laboratory of microRNA Diagnostics and Therapeutics, Van Andel Research Institute, Grand Rapids, Michigan. Electronic address: lorenzo.sempere@vai.org.
Van Andel Institute · USDartmouth–Hitchcock Medical Center · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
A spatially-modulated scatter imaging system to detect tumor-associated stromaR21RR024411 · NCRR · DARTMOUTH COLLEGE · PI WELLS, WENDY ANNE · 2009 to 2010
$397k
microRNAs as novel biomarkers for management of breast cancerR21CA141017 · NCI · DARTMOUTH COLLEGE · PI SEMPERE, LORENZO · 2011 to 2012
$378k
Role of microRNAs in initiation and progression of breast cancerR03CA141564 · NCI · DARTMOUTH COLLEGE · PI SEMPERE, LORENZO · 2009 to 2010
$158k
NCI NIH HHS P30 CA023108NCI NIH HHS R03 CA141564NCI NIH HHS R21 CA141017NCRR NIH HHS R21 RR024411
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is an aggressive subtype defined by the lack of estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 expression. Expression of miR-21, an oncomiR, is frequently altered and may be distinctly expressed in the tumor stroma. Because tumor lesions are a complex mixture of cell types, we hypothesized that analysis of miR-21 expression at single-cell resolution could provide more accurate information to assess disease recurrence risk and BC-related death. We implemented a fully automated, tissue slide-based assay to detect miR-21 expression in 988 patients with BC. The miR-21(High) group exhibited shorter recurrence-free survival [hazard ratio (HR), 1.71; P < 0.001] and BC-specific survival (HR, 1.96; P < 0.001) in multivariate regression analyses. When tumor compartment and levels of miR-21 expression were considered, significant associations with poor clinical outcome were detected exclusively in tumor epithelia from estrogen receptor- and/or progesterone receptor-positive human epidermal growth factor receptor 2-negative cases [recurrence-free survival: HR, 3.67 (P = 0.006); BC-specific survival: HR, 5.13 (P = 0.002)] and in tumor stroma from TNBC cases [recurrence-free survival: HR, 2.59 (P = 0.013); BC-specific survival: HR, 3.37 (P = 0.003)]. These findings suggest that the context of altered miR-21 expression provides clinically relevant information. Importantly, miR-21 expression was predominantly up-regulated and potentially prognostic in the tumor stroma of TNBC.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticAgedCell SurvivalCohort StudiesDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunohistochemistryIn Situ HybridizationMicroRNAsMiddle AgedMultivariate AnalysisPrognosisProportional Hazards ModelsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMicroRNAsMIRN21 microRNA, human

Identifiers

PMID25440114
PMCPMC4258602
OpenAlexW2110144101

What OpenQuestion holds

Textmetadata
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.