Evidence map›Paper›PMID 30922194›Full record

ArticleCancer biology & therapy2019

MicroRNA-4417 is a tumor suppressor and prognostic biomarker for triple-negative breast cancer.

Chen Khuan Wong, Christopher Gromisch, Sait Ozturk, Panagiotis Papageorgis, Hamid Mostafavi Abdolmaleky, Björn M Reinhard, Arunthathi Thiagalingam, Sam Thiagalingam

Abstract read
In one paragraph

Article in Cancer biology & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–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

12 citing papers in PubMed.

  1. The Role of miR-501-3p in Abdominal Aortic Aneurysm Progression: A Pilot Study.Journal of cardiovascular translational research · 2026
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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.

Chen Khuan Wonga Graduate Program in Genetics and Genomics , Boston University School of Medicine , Boston , MA , USA.
Christopher Gromischc Department of Pharmacology & Experimental Therapeutics , Boston University School of Medicine , Boston , MA , USA.
Sait Ozturkd Graduate Program in Molecular and Translational Medicine , Boston University School of Medicine , Boston , MA , USA.
Panagiotis Papageorgisf Department of Life Sciences , School of Sciences, European University Cyprus , Nicosia , Cyprus.
Hamid Mostafavi Abdolmalekyb Biomedical Genetics Section, Department of Medicine , Boston University School of Medicine , Boston , MA , USA.
Björn M Reinhardg Department of Chemistry , Boston University , Boston , MA , USA.
Arunthathi Thiagalingamb Biomedical Genetics Section, Department of Medicine , Boston University School of Medicine , Boston , MA , USA.
Sam Thiagalingama Graduate Program in Genetics and Genomics , Boston University School of Medicine , Boston , MA , USA.ORCID 0000-0001-5211-266X

Funding

Project-005UL1TR001430 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BAIR-MERRITT, MEGAN H, CENTER, DAVID M. · 2015 to 2024
$52.3M
Boston University Clinical and Translational Science Award (CTSA) Program UL1UL1TR000157 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M. · 2012 to 2013
$7.9M
Illuminating Dynamic Receptor Clustering in the Epidermal Growth Factor Receptor Signal Transduction Pathway Using Plasmon CouplingR01CA138509 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI Bjoern Markus Reinhard · 2009 to 2026
$5.9M
Translational Research in BiomaterialsT32EB006359 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MARK W. GRINSTAFF, Michelle H Teplensky · 2009 to 2026
$4.2M
Dissecting the metastasis suppressor complex to identify colon cancer biomarkersR21CA165707 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI THIAGALINGAM, SAM · 2013 to 2014
$386k
NCATS NIH HHS UL1 TR000157NCATS NIH HHS UL1 TR001430NCI NIH HHS R01 CA138509NCI NIH HHS R21 CA165707NIBIB NIH HHS T32 EB006359
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is the most aggressive form of breast cancer with poor prognosis due to lack of druggable targets such as hormone and growth factor receptors. Therefore, identification of targetable regulators such as miRNAs could provide new avenues for therapeutic applications. Here, we report that the expression of miR-4417 is suppressed during the progression of TNBC cells from non-malignant to the malignant stage. MiR-4417 is localized to chromosome 1p36, a region with high frequency of loss of heterozygosity in multiple cancers, and its biogenesis is DICER-dependent. Low expression of miR-4417 is significantly associated with worse prognosis in TNBC patients, while overexpression of miR-4417 is sufficient to inhibit migration and mammosphere formation of TNBC cells

Indexed as

Biomarkers, TumorGenes, Tumor SuppressorCell Line, TumorCell MovementCell ProliferationDisease ProgressionEpithelial CellsEpithelial-Mesenchymal TransitionFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMicroRNAsPrognosisRNA InterferenceBiomarkers, TumorMicroRNAsMIRN4717 microRNA, humanepithelial-mesencyhmal transitionmiRNATriple-negative breast cancertumor suppressor

Identifiers

PMID30922194
PMCPMC6605987

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.