Evidence map›Paper›PMID 36645429›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2023

Doxorubicin-induced acute cardiotoxicity is associated with increased oxidative stress, autophagy, and inflammation in a murine model.

Patricia Lorena Dulf, Mihaela Mocan, Camelia Alexandra Coadă, Daniel Vasile Dulf, Remus Moldovan, Ioana Baldea, Anca-Daniela Farcas, Dan Blendea, Adriana Gabriela Filip

Open access · hybridAbstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
15.1field-weighted citation impact, top 1% 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

41 citing papers in PubMed, 69 citations in OpenAlex.

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  19. Doxorubicin-Induced Cardiotoxicity: A Comprehensive Update.Journal of cardiovascular development and disease · 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

9 authors at 2 institutions in 3 countries.

Patricia Lorena DulfIuliu Hatieganu University of Medicine and Pharmacy, 400012, Cluj-Napoca-Napoca, Romania.
Mihaela MocanEmergency Clinical County Hospital, 40006, Cluj-Napoca-Napoca, Romania. mihaela.mocan@gmail.com.
Camelia Alexandra CoadăDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138, Bologna, Italy. camelia.coada@unibo.it.
Daniel Vasile DulfIuliu Hatieganu University of Medicine and Pharmacy, 400012, Cluj-Napoca-Napoca, Romania.
Remus MoldovanDepartment of Functional Biosciences, Iuliu Hatieganu University of Medicine and Pharmacy, 400012, Cluj-Napoca-Napoca, Romania.
Ioana BaldeaDepartment of Functional Biosciences, Iuliu Hatieganu University of Medicine and Pharmacy, 400012, Cluj-Napoca-Napoca, Romania.
Anca-Daniela FarcasDepartment of Internal Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, 400012, Cluj-Napoca-Napoca, Romania.
Dan BlendeaDepartment of Internal Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, 400012, Cluj-Napoca-Napoca, Romania.
Adriana Gabriela FilipDepartment of Functional Biosciences, Iuliu Hatieganu University of Medicine and Pharmacy, 400012, Cluj-Napoca-Napoca, Romania.
Iuliu Hațieganu University of Medicine and Pharmacy · ROUniversity of Bologna · IT

Funding

European Social Found, Human Capital Operational Programme 2014-2020 POCU/380/6/13/125171"Iuliu Hatieganu" University of Medicine and Pharmacy Cluj-Napoca 1529/13/18.01.2019
6 · The paper itself

Abstract

Drug-induced cardiotoxicity is a life-threatening side effect of doxorubicin (DOX) treatment that impacts patient prognosis and survival. In the majority of cases, the acute clinical form often remains asymptomatic, with few patients presenting rather nonspecific electrocardiographic abnormalities. While chronic toxicity has been more widely studied, the alterations appearing in acute cardiotoxicity are much less investigated. Thus, our in vivo study aimed to evaluate the process of DOX-induced acute myocardial toxicity by investigating oxidative stress and autophagy markers as mechanisms of myocardial toxicity in correlation with echocardiography and electrocardiography findings. Our results show that both autophagy and oxidative homeostasis were disrupted as soon as 7 days after DOX treatment, alterations that occurred even before the significant increase of NT-proBNP, a clinical marker for cardiac suffering. Moreover, we found a large number of alterations in the electrocardiography and echocardiography of treated rats. These findings suggest that DOX-induced myocardial toxicity started early after treatment initiation, possibly marking the initial phase of the unfolding process of cardiac damage. Further studies are required to completely decipher the mechanisms of DOX-induced cardiotoxicity.

Indexed as

CardiotoxicityDoxorubicinAnimalsAntibiotics, AntineoplasticApoptosisAutophagyDisease Models, AnimalInflammationMiceMyocytes, CardiacOxidative StressRatsAntibiotics, AntineoplasticDoxorubicinAutophagyCardiotoxicityChemotherapyDoxorubicin side-effectsOxidative stressUltrasonography

Identifiers

PMID36645429
PMCPMC10185623
OpenAlexW4316466731

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.