Evidence map›Paper›PMID 29923083›Full record

ReviewJournal of cancer research and clinical oncology2018

MicroRNAs in regulation of triple-negative breast cancer progression.

Dominika Piasecka, Marcin Braun, Radzislaw Kordek, Rafal Sadej, Hanna Romanska

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

95 citing papers in PubMed, 182 citations in OpenAlex.

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  11. Harnessing the Role ofInternational journal of molecular sciences · 2025
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35 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Dominika PiaseckaDepartment of Pathology, Medical University of Lodz, Lodz, Poland.ORCID http://orcid.org/0000-0001-5360-6477
Marcin BraunDepartment of Pathology, Medical University of Lodz, Lodz, Poland.ORCID http://orcid.org/0000-0003-3804-7042
Radzislaw KordekDepartment of Pathology, Medical University of Lodz, Lodz, Poland.ORCID http://orcid.org/0000-0003-4724-3627
Rafal SadejDepartment of Molecular Enzymology, Intercollegiate Faculty of Biotechnology, University of Gdansk and Medical University of Gdansk, Gdansk, Poland. rsadej@gumed.edu.pl.ORCID http://orcid.org/0000-0003-2583-7299
Hanna RomanskaDepartment of Pathology, Medical University of Lodz, Lodz, Poland. hanna.romanska@gmail.com.ORCID http://orcid.org/0000-0002-2328-710X
Medical University of Lodz · PLGdańsk Medical University · PLMedical University of Warsaw · PL

Funding

Narodowe Centrum Nauki UMO-2015/17/B/ NZ4/02157
6 · The paper itself

Abstract

purposeDysregulation of miRNA profile has been associated with a broad spectrum of cellular processes underlying progression of various human malignancies. Increasing evidence suggests that specific microRNA clusters might be of clinical utility, especially in triple-negative breast carcinoma (TNBC), devoid of both predictive markers and potential therapeutic targets. Here we provide a comprehensive review of the existing data on microRNAs in TNBC, their molecular targets, a putative role in invasive progression with a particular emphasis on the epithelial-to-mesenchymal transition (EMT) and acquisition of stem-cell properties (CSC), regarded both as prerequisites for metastasis, and significance for therapy.

methodsPubMed and Medline databases were systematically searched for the relevant literature. 121 articles have been selected and thoroughly analysed.

resultsSeveral miRNAs associated with EMT/CSC and invasion were identified as significantly (1) upregulated: miR-10b, miR-21, miR-29, miR-9, miR-221/222, miR-373 or (2) downregulated: miR-145, miR-199a-5p, miR-200 family, miR-203, miR-205 in TNBC. Dysregulation of miR-10b, miR-21, miR-29, miR-145, miR-200 family, miR-203, miR-221/222 was reported of prognostic value in TNBC patients.

conclusionAvailable data suggest that specific microRNA clusters might play an important role in biology of TNBC, understanding of which should assist disease prognostication and therapy.

Indexed as

Gene Expression Regulation, NeoplasticDisease ProgressionFemaleHumansMicroRNAsTriple Negative Breast NeoplasmsMicroRNAsCSCEMTInvasionMicroRNATriple-negative breast carcinoma

Identifiers

PMID29923083
PMCPMC6061037
OpenAlexW2809133542

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.