Evidence map›Paper›PMID 30622242›Full record

ArticleCell death & disease2019

Argonaute 2 drives miR-145-5p-dependent gene expression program in breast cancer cells.

Teresa Bellissimo, Claudia Tito, Federica Ganci, Andrea Sacconi, Silvia Masciarelli, Giuseppe Di Martino, Natale Porta, Mirko Cirenza, Melissa Sorci, Luciana De Angelis and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  5. miR-145-5p Inhibits HER2-Positive Breast Cancer Cells via Targeting ARF6.International journal of general medicine · 2025
    Article
  6. MiR-145-5p regulates granulosa cell proliferation by targeting theThe Journal of reproduction and development · 2024
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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

17 authors at 4 institutions in 3 countries.

Teresa BellissimoDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Claudia TitoDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Federica GanciOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Andrea SacconiOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Silvia MasciarelliDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Giuseppe Di MartinoDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Pathology Unit, ICOT, Latina, Italy.
Natale PortaDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Pathology Unit, ICOT, Latina, Italy.ORCID http://orcid.org/0000-0002-0548-744X
Mirko CirenzaDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Pathology Unit, ICOT, Latina, Italy.
Melissa SorciDepartment of Biology and Biotechnology "C. Darwin", Sapienza University of Rome, Rome, Italy.
Luciana De AngelisDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy.
Paolo RosaDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Pathology Unit, ICOT, Latina, Italy.ORCID http://orcid.org/0000-0002-8468-0677
Antonella CalogeroDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Pathology Unit, ICOT, Latina, Italy.
Alessandro FaticaDepartment of Biology and Biotechnology "C. Darwin", Sapienza University of Rome, Rome, Italy.
Vincenzo PetrozzaDepartment of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Pathology Unit, ICOT, Latina, Italy.
Giulia FontemaggiOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy. giulia.fontemaggi@ifo.gov.it.
Giovanni BlandinoOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy. giovanni.blandino@ifo.gov.it.
Francesco FaziDepartment of Anatomical, Histological, Forensic & Orthopedic Sciences, Section of Histology & Medical Embryology, Sapienza University of Rome, laboratory affiliated to Istituto Pasteur Italia-Fondazione Cenci Bolognetti, Rome, Italy. francesco.fazi@uniroma1.it.
Sapienza University of Rome · ITIstituto Pasteur · ITEpigenomics (Germany) · DENational Cancer Institute · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To perform their regulatory functions, microRNAs (miRNAs) must assemble with any of the four mammalian Argonaute (Ago) family of proteins, Ago1-4, into an effector complex known as the RNA-induced silencing complex (RISC). While the mature miRNA guides the RISC complex to its target mRNA, the Ago protein represses mRNA translation. The specific roles of the various Ago members in mediating miRNAs activity, however, haven't been clearly established. In this study, we investigated the contribution of Ago2, the only human Ago protein endowed with nuclease activity, to the function of tumor-suppressor miR-145-5p in breast cancer (BC). We show that miR-145-5p and Ago2 protein are concomitantly downregulated in BC tissues and that restoration of miR-145-5p expression in BC cells leads to Ago2 protein induction through the loosening of Ago2 mRNA translational repression. Functionally, miR-145-5p exerts its inhibitory activity on cell migration only in presence of Ago2, while, upon Ago2 depletion, we observed increased miR-145/Ago1 complex and enhanced cell motility. Profiling by microarray of miR-145-5p target mRNAs, in BC cells depleted or not of Ago2, revealed that miR-145-5p drives Ago2-dependent and -independent activities. Our results highlight that the Ago2 protein in cancer cells strictly dictates miR-145-5p tumor suppressor activity.

Indexed as

Gene ExpressionA549 CellsArgonaute ProteinsBreast NeoplasmsCell CycleCell MovementEukaryotic Initiation FactorsFemaleHumansKaplan-Meier EstimateMCF-7 CellsMicroRNAsPolyribosomesProtein BiosynthesisTransfectionAGO1 protein, humanAGO2 protein, humanArgonaute ProteinsEukaryotic Initiation FactorsMicroRNAsMIRN145 microRNA, human

Identifiers

PMID30622242
PMCPMC6325137
OpenAlexW2908591641

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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.