Evidence map›Paper›PMID 39065634›Full record

ArticlePharmaceutics2024

Design and Optimization of Sesamol Nanosuspensions to Potentiate the Anti-Tumor Activity of Epirubicin against Ehrlich Solid Carcinoma-Bearing Mice.

Kholoud A Elzanaty, Gamal A Omran, Ehab Kotb Elmahallawy, Ashraf Albrakati, Ayman A Saleh, Naief Dahran, Alaa S Alhegaili, Ahmad Salahuddin, Heba Abd-El-Azim, Ahmed Noreldin and 1 more

Abstract read
In one paragraph

Article in Pharmaceutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

11 authors.

Kholoud A ElzanatyDepartment of Biochemistry, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.
Gamal A OmranDepartment of Biochemistry, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.ORCID 0000-0002-1609-8802
Ehab Kotb ElmahallawyGrupo de Investigación en Sanidad Animal y Zoonosis (GISAZ), Departamento de Sanidad Animal, Universidad de Córdoba, 14071 Córdoba, Spain.
Ashraf AlbrakatiDepartment of Human Anatomy, College of Medicine, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.ORCID 0000-0002-4116-7865
Ayman A SalehDepartment of Pathology, College of Medicine, University of Hail, Hail 55428, Saudi Arabia.
Naief DahranDepartment of Anatomy, Faculty of Medicine, University of Jeddah, Jeddah 21959, Saudi Arabia.ORCID 0000-0003-3560-8166
Alaa S AlhegailiDepartment of Medical Laboratory, College of Applied Medical Sciences, Prince Sattam bin Abdulaziz University, Al-Kharj 11942, Saudi Arabia.ORCID 0000-0002-0984-167X
Ahmad SalahuddinDepartment of Biochemistry, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.ORCID 0000-0002-7382-4284
Heba Abd-El-AzimDepartment of Pharmaceutics, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.ORCID 0000-0002-4740-6740
Ahmed NoreldinDepartment of Histology and Cytology, Faculty of Veterinary Medicine, Damanhour University, Damanhour 22511, Egypt.ORCID 0000-0002-8344-0807
Tarek M OkdaDepartment of Biochemistry, Faculty of Pharmacy, Damanhour University, Damanhour 22511, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a growing interest in discovering natural sources of anti-cancer drugs. Sesamol (SES) is a phenolic compound with antitumor effects. The present study aimed to investigate the anticancer properties of SES and its nano-suspensions (SES-NS) combined with Epirubicin (EPI) in breast cancer (BC) using mice bearing a solid Ehrlich tumor. The study involved 35 female albino mice and investigated the effects of SES and EPI on tumor growth, proliferation, apoptosis, autophagy, angiogenesis, and oxidative stress. Methods including ELISA, qRT-PCR, and immunohistochemistry were utilized. The findings revealed reductions in tumor growth and proliferation using SES either alone or combined and evidenced by decreased AKT (AKT Serine/Threonine kinase1) levels, angiogenesis indicated by lower levels of VEGFR (vascular endothelial growth factor), and apoptosis demonstrated by elevated caspase3 and BAX levels. Furthermore, autophagy increased and was indicated by increased levels of beclin1 and lc3, along with decreased oxidative stress as evidenced by elevated TAC (total antioxidant capacity) and reduced MDA (malondialdehyde) levels. Interestingly, SES-NS demonstrated more significant effects at lower doses. In summary, this study underscores the potential of SES as a promising agent for BC treatment. Moreover, SES-NS potentiated the beneficial effects of EPI while mitigating its adverse effects.

Indexed as

angiogenesisapoptosisautophagybreast cancerEhrlich solid tumorEpirubicinsesamol

Identifiers

PMID39065634
PMCPMC11279961

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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.