Evidence map›Paper›PMID 34797887›Full record

ArticlePloS one2021

Hsa-miR-21-3p associates with breast cancer patient survival and targets genes in tumor suppressive pathways.

Arsalan Amirfallah, Hildur Knutsdottir, Adalgeir Arason, Bylgja Hilmarsdottir, Oskar T Johannsson, Bjarni A Agnarsson, Rosa B Barkardottir, Inga Reynisdottir

Abstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

29 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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.

Arsalan AmirfallahCell Biology Unit, Department of Pathology, Landspitali-The National University Hospital of Iceland, Reykjavik, Iceland.
Hildur KnutsdottirDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America.
Adalgeir ArasonBiomedical Center, Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Bylgja HilmarsdottirBiomedical Center, Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Oskar T JohannssonDepartment of Pathology, Landspitali-The National University Hospital of Iceland, Reykjavik, Iceland.
Bjarni A AgnarssonDepartment of Oncology, Landspitali-The National University Hospital of Iceland, Reykjavik, Iceland.
Rosa B BarkardottirBiomedical Center, Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Inga ReynisdottirCell Biology Unit, Department of Pathology, Landspitali-The National University Hospital of Iceland, Reykjavik, Iceland.ORCID 0000-0002-9730-7476

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the cancer most often diagnosed in women. MicroRNAs (MIRs) are short RNA molecules that bind mRNA resulting in their downregulation. MIR21 has been shown to be an oncomiR in most cancer types, including breast cancer. Most of the effects of miR-21 have been attributed to hsa-miR-21-5p that is transcribed from the leading strand of MIR21, but hsa-miR-21-3p (miR-21-3p), transcribed from the lagging strand, is much less studied. The aim of the study is to analyze whether expression of miR-21-3p is prognostic for breast cancer. MiR-21-3p association with survival, clinical and pathological characteristics was analyzed in a large breast cancer cohort and validated in three separate cohorts, including TCGA and METABRIC. Analytical tools were also used to infer miR-21-3p function and to identify potential target genes and functional pathways. The results showed that in the exploration cohort, high miR-21-3p levels associated with shorter survival and lymph node positivity. In the three validation cohorts, high miR-21-3p levels associated with pathological characteristics that predict worse prognosis. Specifically, in the largest validation cohort, METABRIC (n = 1174), high miR-21-3p levels associated with large tumors, a high grade, lymph node and HER2 positivity, and shorter breast-cancer-specific survival (HR = 1.38, CI 1.13-1.68). This association remained significant after adjusting for confounding factors. The genes with expression levels that correlated with miR-21-3p were enriched in particular pathways, including the epithelial-to-mesenchymal transition and proliferation. Among the most significantly downregulated targets were MAT2A and the tumor suppressive genes STARD13 and ZNF132. The results from this study emphasize that both 3p- and 5p-arms from a MIR warrant independent study. The data show that miR-21-3p overexpression in breast tumors is a marker of worse breast cancer progression and it affects genes in pathways that drive breast cancer by down-regulating tumor suppressor genes. The results suggest miR-21-3p as a potential biomarker.

Indexed as

Biomarkers, TumorBreast NeoplasmsCancer SurvivorsCell ProliferationCohort StudiesDown-RegulationEpithelial-Mesenchymal TransitionFemaleGene ExpressionGTPase-Activating ProteinsHumansLymph NodesMicroRNAsSignal TransductionTumor Suppressor ProteinsBiomarkers, TumorGTPase-Activating ProteinsMicroRNAsMIRN21 microRNA, humanTumor Suppressor Proteins

Identifiers

PMID34797887
PMCPMC8604322

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Registered trials

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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.