Evidence map›Paper›PMID 30627229›Full record

ArticleDisease markers2018

A Specific Circulating MicroRNA Cluster Is Associated to Late Differential Cardiac Response to Doxorubicin-Induced Cardiotoxicity

Clarissa Ruggeri, Sonia Gioffré, Mattia Chiesa, Marta Buzzetti, Giuseppina Milano, Alessandro Scopece, Laura Castiglioni, Marta Pontremoli, Luigi Sironi, Giulio Pompilio and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

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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

12 authors at 3 institutions in 2 countries.

Clarissa RuggeriImmunology and Functional Genomics Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Sonia GioffréImmunology and Functional Genomics Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Mattia ChiesaImmunology and Functional Genomics Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Marta BuzzettiImmunology and Functional Genomics Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Giuseppina MilanoVascular Biology and Regenerative Medicine Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Alessandro ScopeceVascular Biology and Regenerative Medicine Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Laura CastiglioniDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.ORCID 0000-0002-0772-3231
Marta PontremoliImmunology and Functional Genomics Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Luigi SironiDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.ORCID 0000-0002-4738-3454
Giulio PompilioVascular Biology and Regenerative Medicine Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.ORCID 0000-0003-2581-5735
Gualtiero I ColomboImmunology and Functional Genomics Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.
Yuri D'AlessandraImmunology and Functional Genomics Unit, Centro Cardiologico Monzino IRCCS, Milan, Italy.ORCID 0000-0002-3440-2353
Centro Cardiologico Monzino · ITUniversity of Milan · ITUniversity Hospital of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiotoxicity is a detrimental side effect of the anticancer drug doxorubicin (DOX), characterized by progressive heart dysfunction. Circulating microRNAs (miRNAs) are recognized as potential biomarkers of cardiac disease; thus, we aimed to investigate their association with late cardiotoxicity in an animal model of disease.

methodsTwenty C57BL/6 female mice were administered with 24 mg/kg cumulative dose of DOX or saline during 2 weeks, followed by a recovery period of one month (T42). Echocardiography was performed at baseline and at T42, and plasma samples were collected at T42. The selection of all miRNAs of interest was conducted by literature overview and by screening, followed by RT-qPCR validation

conclusionThis is the first study indicating that, similarly to what is observed in patients, DOX-administered animals present a differential cardiac response to treatment. Moreover, our results indicate the presence of specific plasma miRNAs whose expression reflect the presence of cardiac dysfunction in response to drug-induced injury.

Indexed as

Genetic MarkersAnimalsCardiotoxicityCirculating MicroRNADisease Models, AnimalDoxorubicinEchocardiographyFemaleHumansMiceMice, Inbred C57BLMicroRNAsMultigene FamilyCirculating MicroRNADoxorubicinGenetic MarkersMicroRNAsMirn133 microRNA, mouseMirn1 microRNA, mouseMIRN34a microRNA, mouseMIRN499 microRNA, mouse

Identifiers

PMID30627229
PMCPMC6304816
OpenAlexW2904760209

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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.