Evidence map›Paper›PMID 29324832›Full record

ArticlePloS one2018

Differential microRNA expression in breast cancer with different onset age.

Hsiu-Pei Tsai, Shiang-Fu Huang, Chien-Fan Li, Huei-Tzu Chien, Shin-Cheh Chen

Open access · goldAbstract read
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 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 78 citations in OpenAlex.

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  13. 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
  14. Article
  15. Longitudinal evaluation of whole blood miRNA expression in firefighters.Journal of exposure science & environmental epidemiology · 2021
    Article
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  18. Observational
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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.

Hsiu-Pei TsaiGraduate Institute of Clinical Medical Sciences, Chang Gung University, Gueishan, Taoyuan, Taiwan.
Shiang-Fu HuangGraduate Institute of Clinical Medical Sciences, Chang Gung University, Gueishan, Taoyuan, Taiwan.
Chien-Fan LiDepartment of Public Health, Chang Gung University, Gueishan, Taoyuan, Taiwan.
Huei-Tzu ChienDepartment of Public Health, Chang Gung University, Gueishan, Taoyuan, Taiwan.ORCID 0000-0002-4120-7070
Shin-Cheh ChenDepartment of General Surgery, Chang Gung Memorial Hospital, Gueishan, Taoyuan, Taiwan.
Chang Gung University · TWChang Gung Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe lower breast cancer incidence in Asian populations compared with Western populations has been speculated to be caused by environmental and genetic variation. Early-onset breast cancer occupies a considerable proportion of breast cancers in Asian populations, but the reason for this is unclear. We aimed to examine miRNA expression profiles in different age-onset groups and pathological subtypes in Asian breast cancer.

methodsAt the first stage, 10 samples (tumor: n = 6, normal tissue: n = 4) were analyzed with an Agilent microRNA 470 probe microarray. Candidate miRNAs with expression levels that were significantly altered in breast cancer samples or selected from a literature review were further validated by quantitative real-time PCR (qPCR) of 145 breast cancer samples at the second stage of the process. Correlations between clinicopathological parameters of breast cancer patients from different age groups and candidate miRNA expression were elucidated.

resultsIn the present study, the tumor subtypes were significantly different in each age group, and an onset age below 40 had poor disease-free and overall survival rates. For all breast cancer patients, miR-335 and miR-145 were down-regulated, and miR-21, miR-200a, miR-200c, and miR-141 were up-regulated. In very young patients (age < 35 y/o), the expression of 3 and 8 specific miRNAs were up- and down-regulated, respectively. In young patients (36-40 y/o), 3 and 3 specific miRNAs were up- and down-regulated, respectively. miR-532-5p was up-regulated in triple-negative breast cancer.

conclusionsDifferential miRNA expressions between normal and tumor tissues were observed in different age groups and tumor subtypes. Evolutionarily conserved miRNA clusters, which initiate malignancy transformation, were up-regulated in the breast cancers of very young patients. None of the significantly altered miRNAs were observed in postmenopausal patients.

Indexed as

AdultAgedAge of OnsetAsian PeopleBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesFemaleGene Expression ProfilingHumansKaplan-Meier EstimateMicroRNAsMiddle AgedOligonucleotide Array Sequence AnalysisPrognosisReal-Time Polymerase Chain ReactionReceptors, EstrogenERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMicroRNAsReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID29324832
PMCPMC5764434
OpenAlexW2782898644

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LicenceCC BY
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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.