Evidence map›Paper›PMID 39762303›Full record

ArticleScientific reports2025

Unveiling the potential anticancer activity of Spirulina maxima extract-nanoemulsion through in vitro and in vivo studies.

Mohammed Yasser Hussein, Merna Nasr, Veronia Emad, Julie Maged, Portia George, Amina Emad, Abeer Mahmoud Badr, Mehrez E El-Naggar, Sayeda M Abdo, Jihan Hussein

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

10 authors.

Mohammed Yasser HusseinBiotechnology Program, Faculty of Science, Cairo University, Giza, 12612, Egypt. MohammedYMMH@gmail.com.
Merna NasrBiotechnology Program, Faculty of Science, Cairo University, Giza, 12612, Egypt.
Veronia EmadBiotechnology Program, Faculty of Science, Cairo University, Giza, 12612, Egypt.
Julie MagedBiotechnology Program, Faculty of Science, Cairo University, Giza, 12612, Egypt.
Portia GeorgeBiotechnology Program, Faculty of Science, Cairo University, Giza, 12612, Egypt.
Amina EmadBiotechnology Program, Faculty of Science, Cairo University, Giza, 12612, Egypt.
Abeer Mahmoud BadrZoology Department, Faculty of Science, Cairo University, Giza, 12612, Egypt.
Mehrez E El-NaggarTextile Research Division, National Research Centre, Giza, 12622, Egypt.
Sayeda M AbdoWater Pollution Research Department, National Research Centre, Giza, 12622, Egypt.
Jihan HusseinMedical Biochemistry Department, National Research Centre, Giza, 12622, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Being the second leading cause of death globally, cancer has been a long-standing and rapidly evolving focus of biomedical research and practice in the world. Recently, there has been growing interest in cyanobacteria. This focus is particularly evident in developing innovative anticancer treatments to reduce reliance on traditional chemotherapy. This study investigates the anticancer potential of the Spirulina maxima extract nanoemulsion (SMNE) technique to improve the delivery, stability, and solubility of the S. maxima extract (SME). SMNE, prepared in three concentrations (SMNEC1, SMNEC2, SMNEC3), was characterized and confirmed to successfully load SME into silica-coated nanoparticles. Cytotoxicity tests on HepG2 and MCF-7 cell lines revealed a significant reduction in cell viability after 48-hour SMNE treatment, with IC50 values of 1488 µg/mL and 1721.936 µg/mL, respectively. SMNE also demonstrated efficacy in inhibiting tumor growth in mice with Ehrlich ascites carcinoma, normalizing alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, and reducing oxidative stress markers such as catalase (CAT) and malondialdehyde (MDA). Histopathological examination showed that SMNEC3-treated groups had almost normal liver architecture. Additionally, SMNE downregulated oncogenic miR-221-3p and miR-222-3p, activating cancer suppression genes p27 and PTEN. The study concludes that SMNE, with its anti-inflammatory and antioxidant properties and ability to modulate key miRNAs, enhances SME delivery and shows promise as an effective cancer treatment.

Indexed as

Antineoplastic AgentsEmulsionsNanoparticlesSpirulinaAnimalsCarcinoma, Ehrlich TumorCell SurvivalHep G2 CellsHumansMCF-7 CellsMiceOxidative StressAntineoplastic AgentsEmulsionsEAC modelGallic acidHepG2 cellsMCF-7 cellsmiR-221-3pmiR-222-3p

Identifiers

PMID39762303
PMCPMC11704349

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.