Evidence map›Paper›PMID 38098043›Full record

ArticleBMC complementary medicine and therapies2023

Evaluation of antioxidant, anti-inflammatory, anticancer activities and molecular docking of Moringa oleifera seed oil extract against experimental model of Ehrlich ascites carcinoma in Swiss female albino mice.

Tahany Saleh Aldayel, Heba N Gad El Hak, Mohamed S Nafie, Raneem Saad, Heba M A Abdelrazek, Omnia E Kilany

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 9 citations in OpenAlex.

  1. Optimized CoQ10 deliveryRSC advances · 2026
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  8. HarnessingInternational journal of molecular sciences · 2025
    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

6 authors at 2 institutions in 2 countries.

Tahany Saleh AldayelDepartment of Health Sciences, Clinical Nutrition, College of Health and Rehabilitation Sciences, Princess Nourah bint Abdulrahman University, Riyadh, 11671, Saudi Arabia.
Heba N Gad El HakDepartment of Zoology, Faculty of Science, Suez Canal University, Ismailia, Egypt. heba_ahmed@science.suez.edu.eg.
Mohamed S NafieChemistry Department, Faculty of Science, Suez Canal University, Ismailia, 41522, Egypt.
Raneem SaadDepartment of Clinical Pathology, Faculty of Veterinary Medicine, Suez Canal University, Ismailia, Egypt.
Heba M A AbdelrazekDepartment of Physiology, Faculty of Veterinary Medicine, Suez Canal University, Ismailia, Egypt.
Omnia E KilanyDepartment of Clinical Pathology, Faculty of Veterinary Medicine, Suez Canal University, Ismailia, Egypt.
Suez Canal University · EGPrincess Nourah bint Abdulrahman University · SA

Funding

Princess Nourah Bint Abdulrahman University PNURSP2022R74
6 · The paper itself

Abstract

The current research intended to evaluate the antitumor properties of Moringa oleifera oil extract (MOE). Fifty-six female Swiss albino mice were employed in this study. Animals were assigned into four groups: control (C) group, moringa oil extract (MOE) group administered (500 mg/kg b. wt) MOE daily via gavage, Ehrlich ascites carcinoma (EAC) group and EAC group administered daily with (500 mg/kg b.wt) MOE for two weeks (EAC/MOE). The results showed that MOE significantly ameliorated the EAC increase in body weight and reduced the EAC cell viability. In addition, they upgraded the levels of hepatic and renal functions, inflammatory cytokines, oxidative stress markers and EAC-induced hepatic and renal histopathological changes. Treatment of EAC with MOE induced antitumor, anti-inflammatory and antioxidant effects and normalized most of the tested parameters besides the histopathological alterations in both renal and hepatic tissues. HPLC for the MOE identified Cinnamic acid, Ellagic acid, Quercetin, Gallic acid, Vanillin and Hesperidin as major compounds. The molecular docking study highlighted the virtual binding of the identified compounds inside the GSH and SOD proteins, especially for Quercetin which exhibited promising binding affinity with good interactive binding mode with the key amino acids. These results demonstrate that the antitumor constituents of MOE against EAC induced oxidative stress and inflammation by preventing oxidative damage and controlling EAC increase.

Indexed as

Carcinoma, Ehrlich TumorMoringa oleiferaAnimalsAnti-Inflammatory AgentsAntioxidantsAscitesFemaleMiceMolecular Docking SimulationPlant ExtractsPlant OilsQuercetinAnti-Inflammatory AgentsAntioxidantsPlant ExtractsPlant OilsQuercetinAntioxidantsCytokinesEhrlich ascites carcinomaKidneyLiverMoringa olifera oil extract

Identifiers

PMID38098043
PMCPMC10720142
OpenAlexW4389742147

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.