Evidence map›Paper›PMID 35682646›Full record

ArticleInternational journal of molecular sciences2022

Prophylactic Evidence of MSCs-Derived Exosomes in Doxorubicin/Trastuzumab-Induced Cardiotoxicity: Beyond Mechanistic Target of NRG-1/Erb Signaling Pathway.

Nesrine Ebrahim, Hajir A Al Saihati, Ola Mostafa, Amira Hassouna, Sameh Abdulsamea, Eman Abd El Aziz M El Gebaly, Nashwa Hassan Abo-Rayah, Dina Sabry, Mohamed El-Sherbiny, Abdelmonem G Madboly and 6 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
2.6field-weighted citation impact, top 9% 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, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Signaling pathways and potential therapeutic agents in trastuzumab-induced cardiotoxicity.Apoptosis : an international journal on programmed cell death · 2026
    Review
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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

16 authors at 7 institutions in 3 countries.

Nesrine EbrahimDepartment of Medical Histology and Cell Biology, Faculty of Medicine, Benha University, Benha 13511, Egypt.
Hajir A Al SaihatiDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hafr Albatin, Hafr Albatin 39524, Saudi Arabia.
Ola MostafaDepartment of Medical Histology and Cell Biology, Faculty of Medicine, Benha University, Benha 13511, Egypt.
Amira HassounaSchool of Interprofessional Health Studies, Faculty of Health and Environmental Sciences, AUT University, Auckland 1010, New Zealand.
Sameh AbdulsameaDepartment of Paediatrics, Faculty of Medicine, Benha University, Benha 13511, Egypt.
Eman Abd El Aziz M El GebalyDepartment of Clinical Pharmacology, Faculty of Medicine, Benha University, Benha 13511, Egypt.
Nashwa Hassan Abo-RayahDepartment of Clinical Pharmacology, Faculty of Medicine, Benha University, Benha 13511, Egypt.ORCID 0000-0002-1607-3103
Dina SabryDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Badr University in Cairo, Cairo 11562, Egypt.ORCID 0000-0002-6720-3385
Mohamed El-SherbinyDepartment of Basic Medical Sciences, College of Medicine, AlMaarefa University, Riyadh 11597, Saudi Arabia.ORCID 0000-0002-0814-1743
Abdelmonem G MadbolyDepartment of Forensic Medicine & Clinical Toxicology, Faculty of Medicine, Benha University, Benha 13511, Egypt.ORCID 0000-0002-4333-9018
Noha Ibrahim HussienDepartment of Physiology, Faculty of Medicine, Banha University, Benha 13511, Egypt.
Raja El Hasnaoui SaadaniDepartment of Basic Medical Sciences, College of Medicine, Princess Nourah bint Abdulrahman University, Riyadh 11671, Saudi Arabia.
Hasnaa Ali EbrahimDepartment of Basic Medical Sciences, College of Medicine, Princess Nourah bint Abdulrahman University, Riyadh 11671, Saudi Arabia.
Omnia A M BadrDepartment of Genetics and Genetic Engineering, Faculty of Agriculture, Benha University, Benha 13511, Egypt.ORCID 0000-0002-2318-9630
Nehal M ElsherbinyDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Tabuk, Tabuk 71491, Saudi Arabia.ORCID 0000-0001-5167-3377
Rabab F SalimDepartment of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Benha University, Benha 13511, Egypt.
Benha University · EGPrincess Nourah bint Abdulrahman University · SAAlfaisal University · SAAuckland University of Technology · NZCairo University · EGMansoura University · EGUniversity of Hafr Al-Batin · SA

Funding

Princess Nourah Bint Abdulrahman University Researchers Supporting Project number PNURSP2022R171Researchers Supporting Program, AlMaarefa University, Riyadh, Saudi Arabia TUMA Project-2021-35
6 · The paper itself

Abstract

Trastuzumab (Trz) is a humanized monoclonal antibody targeting epidermal growth factor receptor 2 (HER2; ErbB2). The combined administration of Trz and doxorubicin (DOX) has shown potent anti-cancer efficacy; however, this regimen may be accompanied by severe cardiac toxicity. Mesenchymal stem cells (MSCs)-derived exosomes are nanosized vesicles that play a crucial role in cell-cell communication and have shown efficacy in the treatment of various diseases. In this study, we aim to investigate the cardioprotective effects of MSCs-derived exosomes in a DOX/Trz- mediated cardiotoxicity model, and the possible mechanisms underlying these effects are elucidated. Forty-nine male rats were randomly assigned into four groups: Group I (control); Group II (Dox/Trz); Group III (protective group); and Group IV (curative group). Cardiac hemodynamic parameters, serum markers of cardiac injury, oxidative stress indices, and cardiac histopathology were investigated. Further, transcript profile of specific cardiac tissue injury markers, apoptotic markers, and fibrotic markers were analyzed using qRT-PCR, while the protein expressions of pAkt/Akt, pERK/ERK, pJNK/JNK, pJNK/JNK, and pSTAT3/STAT3 were evaluated by ELISA. Additionally, cardiac mirR-21 and miR-26a were assessed. A combined administration of DOX/Trz disrupted redox and Ca

Indexed as

ExosomesMesenchymal Stem CellsAnimalsApoptosisCardiotoxicityDoxorubicinErbB ReceptorsFibrosisMaleMyocytes, CardiacNeuregulin-1Oxidative StressPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRatsSignal TransductionDoxorubicinErbB ReceptorsNeuregulin-1Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTrastuzumabAKTcardiac toxicitydoxorubicinexosomesMAPKNRG-1stem cellstrastuzumab

Identifiers

PMID35682646
PMCPMC9181089
OpenAlexW4281559260

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.