Evidence map›Paper›PMID 37305823›Full record

SynthesisJournal of medicine and life2023

Chemotherapy-induced cardiotoxicity: a new perspective on the role of Digoxin, ATG7 activators, Resveratrol, and herbal drugs.

Hany Akeel Al-Hussaniy, Ali Hikmat Alburghaif, Zahraa Alkhafaje, Mohammed Abdul-Hassan Jabarah Al-Zobaidy, Hayder Mutair Alkuraishy, Gomaa Mostafa-Hedeab, Faizul Azam, Ali Mahmoud Al-Samydai, Zahraa Salam Al-Tameemi, Meena Akeel Naji

Open access · diamondAbstract readSystematic Review
In one paragraph

Synthesis in Journal of medicine and life, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

15 citing papers in PubMed, 40 citations in OpenAlex.

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  14. Cytotoxic Effect of YH239-EE and Its Enantiomer on MCF7 Cell Line.Asian Pacific journal of cancer prevention : APJCP · 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

10 authors at 5 institutions in 4 countries.

Hany Akeel Al-HussaniyDepartment of Pharmacy, Bilad Alrafidain University College, Diyala, Iraq.
Ali Hikmat AlburghaifDepartment of Pharmacy, Ashur University College, Baghdad, Iraq.
Zahraa AlkhafajeDepartment of Pharmacy, Alfarahidi University College, Baghdad, Iraq.
Mohammed Abdul-Hassan Jabarah Al-ZobaidyDr. Hany Akeel Institute, Iraqi Medical Research Center, Baghdad, Iraq.
Hayder Mutair AlkuraishyDepartment of Clinical Pharmacology, College of Medicine, Almustansria University, Baghdad, Iraq.
Gomaa Mostafa-HedeabPharmacology Department & Health Research Unit, Medical College, Jouf University, Jouf, Saudi Arabia.
Faizul AzamDepartment of Pharmaceutical Chemistry and Pharmacognosy, Unaizah College of Pharmacy, Qassim University, Uniazah, Saudi Arabia.
Ali Mahmoud Al-SamydaiPharmacological and Diagnostic Research Centre, Faculty of Pharmacy, Al-Ahliyya Amman University, Amman, Jordan.
Zahraa Salam Al-TameemiDepartment of Pharmacy, Bilad Alrafidain University College, Diyala, Iraq.
Meena Akeel NajiDr. Hany Akeel Institute, Iraqi Medical Research Center, Baghdad, Iraq.
Baghdad Medical City · IQAl-Ahliyya Amman University · JOAl Jouf University · SAAl-Nisour University College · IQAlrafidain University College · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is a major public health problem, and chemotherapy plays a significant role in the management of neoplastic diseases. However, chemotherapy-induced cardiotoxicity is a serious side effect secondary to cardiac damage caused by antineoplastic's direct and indirect toxicity. Currently, there are no reliable and approved methods for preventing or treating chemotherapy-induced cardiotoxicity. Understanding the mechanisms of chemotherapy-induced cardiotoxicity may be vital to improving survival. The independent risk factors for developing cardiotoxicity must be considered to prevent myocardial damage without decreasing the therapeutic efficacy of cancer treatment. This systematic review aimed to identify and analyze the evidence on chemotherapy-induced cardiotoxicity, associated risk factors, and methods to decrease or prevent it. We conducted a comprehensive search on PubMed, Google Scholar, and Directory of Open Access Journals (DOAJ) using the following keywords: "doxorubicin cardiotoxicity", "anthracycline cardiotoxicity", "chemotherapy", "digoxin decrease cardiotoxicity", "ATG7 activators", retrieving 59 articles fulfilling the inclusion criteria. Therapeutic schemes can be changed by choosing prolonged infusion application over boluses. In addition, some agents like Dexrazoxane can reduce chemotherapy-induced cardiotoxicity in high-risk groups. Recent research found that Digoxin, ATG7 activators, Resveratrol, and other medical substances or herbal compounds have a comparable effect on Dexrazoxane in anthracycline-induced cardiotoxicity.

Indexed as

Antineoplastic AgentsDexrazoxanePolyketidesAnthracyclinesCardiotoxicityDigoxinHumansResveratrolAnthracyclinesAntineoplastic AgentsDexrazoxaneDigoxinPolyketidesResveratrolanthracyclinescardiotoxicityfree radicalsneoadjuvant therapy

Identifiers

PMID37305823
PMCPMC10251384
OpenAlexW4380290970

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.