Evidence map›Paper›PMID 40597910›Full record

ArticleBMC biotechnology2025

Evaluating the anticancer efficacy of Chara vulgaris ethanolic extract and selenium nanoformulation in Ehrlich carcinoma mice: role of autophagy and apoptosis.

Maha Alsunbul, Thanaa A El-Masry, Maisra M El-Bouseary, Enas I El Zahaby, Mostafa M El-Sheekh, Mohamed M S Gaballa, Eman Wahsh, Heba Kamel Badawy, Jawaher Abdullah Alamoudi, Reem ALQahtani and 2 more

Abstract read
In one paragraph

Article in BMC biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Frontiers in cellular and infection microbiology · 2026
    Article
  3. Article
  4. Article
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

12 authors.

Maha AlsunbulDepartment of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O.Box 84428, Riyadh, 11671, Saudi Arabia.
Thanaa A El-MasryFaculty of Pharmacy, Department of Pharmacy Practice, Sinai University-Arish Branch, Arish, 45511, Egypt.
Maisra M El-BousearyFaculty of Pharmacy, Department of Microbiology and Immunology, Tanta University, Tanta, Egypt. maysra_mohamed@pharm.tanta.edu.eg.
Enas I El ZahabyFaculty of Pharmacy, Department of Pharmaceutics, Delta University for Science and Technology, Gamasa, 35712, Egypt.
Mostafa M El-SheekhFaculty of Science, Botany Department, Tanta University, Tanta, Egypt.
Mohamed M S GaballaFaculty of Veterinary Medicine, Department of Pathology, Benha University, Toukh, 13736, Egypt.
Eman WahshFaculty of Pharmacy, Department of Pharmacology and Toxicology, Sinai University-Arish Branch, Arish, 45511, Egypt.
Heba Kamel BadawyFaculty of Pharmacy, Department of Biochemistry, Sinai University-Arish Branch, Arish, 45511, Egypt.
Jawaher Abdullah AlamoudiDepartment of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O.Box 84428, Riyadh, 11671, Saudi Arabia.
Reem ALQahtaniDepartment of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O.Box 84428, Riyadh, 11671, Saudi Arabia.
Naifa AlenaziDepartment of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, P.O.Box 84428, Riyadh, 11671, Saudi Arabia.
Maysa M F El-NagarFaculty of Pharmacy, Tanta University, Tanta, 31527, Egypt. maysa_elnagar@outlook.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBioactive compounds with a wide range of chemical compositions and biological functions are found in the Chlorophyceae family. The present work investigated the anticancer effect of ethanolic extract from Chara vulgaris (C. vulgaris) and its selenium nanoformulation (CvSeNPs) against solid Ehrlich carcinoma (SEC).

methodsGas chromatography-mass spectroscopy was used to analyze C. vulgaris, and many analytical methods were used to characterize the biosynthesized CvSeNPs, including zeta potential, particle size, polydispersity index (PDI), SEM, TEM, and FTIR. In addition, mice with SEC were randomly assigned to seven equal groups (n = 6) to investigate possible mechanisms behind the antitumor activity. Group 1: Tumor control, group 2: Tamoxifen (10 mg/kg), group 3: Free SeNPs, group 4: C. vulgaris (25 mg/kg), group 5: C. vulgaris (50 mg/kg), group 6: 25 mg/kg CvSeNPs, group 7: 50 mg/kg CvSeNPs.

resultsGas chromatography-mass spectroscopy analysis of the ethanolic extract of C. vulgaris revealed the presence of several bioactive chemicals that may promote anticancer activity. Protein levels of TNF-α, NF-кB, VEGF, and Bcl-2 were suppressed in the CvSeNPs group (50 mg/kg), whereas those of caspase-3, BAX, P53, P62, LC3, and Beclin1 were increased. Additionally, CvSeNPs significantly exceeded similar dosages of free extract in terms of caspase-3, BAX, Bcl-2, P53, TNF-α, NF-кB, VEGF, P62, LC3, and Beclin1 gene expression.

conclusionThe CvSeNPs mediated their positive anticancer impact, which manifested as a decrease in tumor volume and an improvement in overall survival rate, by promoting autophagy, apoptosis, and lowering inflammation.

Indexed as

Antineoplastic AgentsApoptosisAutophagyCarcinoma, Ehrlich TumorPlant ExtractsSeleniumAnimalsEthanolMaleMiceNanoparticlesAntineoplastic AgentsEthanolPlant ExtractsSeleniumAntitumorChlorophyceaeMicro-algaeSelenium nanoparticlesSolid Ehrlich carcinoma

Identifiers

PMID40597910
PMCPMC12211136

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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.