Evidence map›Paper›PMID 36932446›Full record

ArticleJournal of experimental & clinical cancer research : CR2023

A diagnostic circulating miRNA signature as orchestrator of cell invasion via TKS4/TKS5/EFHD2 modulation in human gliomas.

Ana Belén Díaz Méndez, Andrea Sacconi, Elisa Tremante, Valentina Lulli, Valentina Caprara, Laura Rosanò, Frauke Goeman, Mariantonia Carosi, Marta Di Giuliani, Giulia Vari and 13 more

Open access · goldFull text read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2023. 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
4.3field-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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  12. The new world of RNA diagnostics and therapeutics.Journal of experimental & clinical cancer research : CR · 2023
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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

23 authors at 7 institutions in 1 country.

Ana Belén Díaz Méndez *Department of Research, Advanced Diagnostics and Technological Innovation, Translational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy.
Andrea Sacconi *Biostatistics and Bioinformatics Unit, Clinical Trial Center, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Elisa TremanteDepartment of Research, Advanced Diagnostics and Technological Innovation, Translational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy.
Valentina LulliDepartment of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Valentina CapraraPreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Laura RosanòPreclinical Models and New Therapeutic Agents Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Frauke GoemanSAFU Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Mariantonia CarosiPathology Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Marta Di GiulianiDepartment of Research, Advanced Diagnostics and Technological Innovation, Translational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy.
Giulia VariDepartment of Research, Advanced Diagnostics and Technological Innovation, Translational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy.
Antonio SilvaniNeuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Bianca PolloNeuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Carlo GarufiMedical-Oncology Unit, San Camillo Forlanini Hospital, Rome, Italy.
Sara RamponiMedical-Oncology Unit, San Camillo Forlanini Hospital, Rome, Italy.
Giorgia SimonettiNeuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Emilio CiusaniNeuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Chiara MandojClinical Pathology Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Stefano ScaleraSAFU Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Veronica VillaniNeuro-Oncology Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Agnese PoDepartment of Experimental Medicine, Sapienza University, Rome, Italy.
Elisabetta FerrettiDepartment of Experimental Medicine, Sapienza University, Rome, Italy.
Giulia RegazzoDepartment of Research, Advanced Diagnostics and Technological Innovation, Translational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy. giulia.regazzo@ifo.it.
Maria Giulia RizzoDepartment of Research, Advanced Diagnostics and Technological Innovation, Translational Oncology Research Unit, IRCCS Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy. maria.rizzo@ifo.it.
Istituti di Ricovero e Cura a Carattere Scientifico · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITSapienza University of Rome · ITCarlo Forlanini Hospital · ITInstitute of Molecular Biology and Pathology · ITIstituto Superiore di Sanità · ITUniversity of Rome Tor Vergata · IT

Funding

Associazione Italiana per la Ricerca sul Cancro AIRC21372H2020 Marie Skłodowska-Curie Actions 764281Ministero della Salute SG-2021-12372157
6 · The paper itself

Abstract

backgroundAltered microRNA profiles have been observed not only in tumour tissues but also in biofluids, where they circulate in a stable form thus representing interesting biomarker candidates. This study aimed to identify a microRNA signature as a non-invasive biomarker and to investigate its impact on glioma biology.

methodsMicroRNAs were selected using a global expression profile in preoperative serum samples from 37 glioma patients. Comparison between serum samples from age and gender-matched controls was performed by using the droplet digital PCR. The ROC curve and Kaplan-Meier survival analyses were used to evaluate the diagnostic/prognostic values. The functional role of the identified signature was assessed by gain/loss of function strategies in glioma cells.

resultsA three-microRNA signature (miR-1-3p/-26a-1-3p/-487b-3p) was differentially expressed in the serum of patients according to the isocitrate dehydrogenase (IDH) genes mutation status and correlated with both patient Overall and Progression Free Survival. The identified signature was also downregulated in the serum of patients compared to controls. Consistent with these results, the signature expression and release in the conditioned medium of glioma cells was lower in IDH-wild type cells compared to the mutated counterpart. Furthermore, in silico analysis of glioma datasets showed a consistent deregulation of the signature according to the IDH mutation status in glioma tumour tissues. Ectopic expression of the signature negatively affects several glioma functions. Notably, it impacts the glioma invasive phenotype by directly targeting the invadopodia-related proteins TKS4, TKS5 and EFHD2.

conclusionsWe identified a three microRNA signature as a promising complementary or even an independent non-invasive diagnostic/prognostic biomarker. The signature displays oncosuppressive functions in glioma cells and impacts on proteins crucial for migration and invasion, providing potential targets for therapeutic intervention.

Indexed as

Brain NeoplasmsCirculating MicroRNAGliomaMicroRNAsAdaptor Proteins, Vesicular TransportBiomarkers, TumorCalcium-Binding ProteinsHumansIsocitrate DehydrogenasePrognosisAdaptor Proteins, Vesicular TransportBiomarkers, TumorCalcium-Binding ProteinsCirculating MicroRNAEFHD2 protein, humanIsocitrate DehydrogenaseMicroRNAsCirculating microRNADiagnosisEFHD2GliomaIDHInvasionTKS4TKS5

Identifiers

PMID36932446
PMCPMC10022260
OpenAlexW4327739339

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read67
identifiers read1
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.