Evidence map›Paper›PMID 36426578›Full record

ArticleEMBO molecular medicine2023

MiR-182-3p targets TRF2 and impairs tumor growth of triple-negative breast cancer.

Roberto Dinami, Luca Pompili, Eleonora Petti, Manuela Porru, Carmen D'Angelo, Serena Di Vito, Angela Rizzo, Virginia Campani, Giuseppe De Rosa, Alejandra Bruna and 9 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  11. Emerging biologic and clinical implications of miR-182-5p in gynecologic cancers.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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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

19 authors at 10 institutions in 6 countries.

Roberto Dinami *Translational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-3585-3439
Luca Pompili *Translational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Eleonora Petti *Translational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0001-8189-1906
Manuela PorruTranslational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0002-6614-9110
Carmen D'AngeloTranslational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Serena Di VitoTranslational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Angela RizzoTranslational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0001-5421-3085
Virginia CampaniDepartment of Pharmacy, University Federico II of Naples, Naples, Italy.
Giuseppe De RosaDepartment of Pharmacy, University Federico II of Naples, Naples, Italy.
Alejandra BrunaCRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Violeta SerraVall d'Hebron Institute of Oncology, Barcelona, Spain.ORCID 0000-0001-6620-1065
Miguel ManoFunctional Genomics and RNA-based Therapeutics Laboratory, Center for Neuroscience and Cell Biology (CNC), University of Coimbra, Coimbra, Portugal.ORCID 0000-0003-1922-4824
Mauro GiaccaKing's College London, British Heart Foundation Centre of Research Excellence, School of Cardiovascular Medicine & Sciences, London, UK.ORCID 0000-0003-2927-7225
Carlo LeonettiTranslational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Gennaro CilibertoScientific Direction, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.
Madalena TarsounasDepartment of Oncology, Genome Stability and Tumourigenesis Group, MRC Oxford Institute for Radiation Oncology, University of Oxford, Oxford, UK.ORCID 0000-0002-4273-2870
Antonella StoppacciaroDepartment of Clinical and Molecular Medicine, St. Andrea Hospital, Sapienza University of Rome, Rome, Italy.
Stefan SchoeftnerDepartment of Life Sciences, University of Trieste, Trieste, Italy.
Annamaria BiroccioTranslational Oncology Research Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.ORCID 0000-0003-3198-3532
Istituti di Ricovero e Cura a Carattere Scientifico · ITFederico II University Hospital · ITKing's College London · GBNational Cancer Institute · MYSapienza University of Rome · ITUniversità degli Studi della Tuscia · ITUniversity of Cambridge · GBUniversity of Oxford · GBUniversity of Trieste · ITVall d'Hebron Institute of Oncology · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The telomeric repeat-binding factor 2 (TRF2) is a telomere-capping protein that plays a key role in the maintenance of telomere structure and function. It is highly expressed in different cancer types, and it contributes to cancer progression. To date, anti-cancer strategies to target TRF2 remain a challenge. Here, we developed a miRNA-based approach to reduce TRF2 expression. By performing a high-throughput luciferase screening of 54 candidate miRNAs, we identified miR-182-3p as a specific and efficient post-transcriptional regulator of TRF2. Ectopic expression of miR-182-3p drastically reduced TRF2 protein levels in a panel of telomerase- or alternative lengthening of telomeres (ALT)-positive cancer cell lines. Moreover, miR-182-3p induced DNA damage at telomeric and pericentromeric sites, eventually leading to strong apoptosis activation. We also observed that treatment with lipid nanoparticles (LNPs) containing miR-182-3p impaired tumor growth in triple-negative breast cancer (TNBC) models, including patient-derived tumor xenografts (PDTXs), without affecting mouse survival or tissue function. Finally, LNPs-miR-182-3p were able to cross the blood-brain barrier and reduce intracranial tumors representing a possible therapeutic option for metastatic brain lesions.

Indexed as

MicroRNAsTriple Negative Breast NeoplasmsAnimalsApoptosisCell Line, TumorGene Expression Regulation, NeoplasticHumansMiceTelomereTelomeric Repeat Binding Protein 2MicroRNAsMirn182 microRNA, humanTelomeric Repeat Binding Protein 2TRF2 protein, mousemiR-182-3ptarget therapytelomeresTRF2triple-negative breast cancer

Identifiers

PMID36426578
PMCPMC9832842
OpenAlexW4309935873

What OpenQuestion holds

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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.