Evidence map›Paper›PMID 36723692›Full record

ArticleMedical oncology (Northwood, London, England)2023

Niosomes nanoparticles as a novel approach in drug delivery enhances anticancer properties of chrysin in human ovarian carcinoma cells (SKOV3): an in vitro study.

Mahdieh Tarahomi, Akram Firouzi Amandi, Majid Eslami, Yalda Yazdani, Amir Salek Farrokhi, Fatemeh Ghorbani, Mohammadhossein Taherian, Bahman Yousefi

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2023. 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
3.6field-weighted citation impact, top 7% 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, 15 citations in OpenAlex.

  1. Review
  2. Development ofPharmaceuticals (Basel, Switzerland) · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Chrysin induces cell death and inhibits migration and invasion in squamous cervical carcinoma using a three-dimensional cell culture model.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

8 authors at 3 institutions in 1 country.

Mahdieh TarahomiCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Akram Firouzi AmandiDepartment of Immunology, Tabriz University of Medical Sciences, Semnan, Iran.
Majid EslamiDepartment of Bacteriology and Virology, Semnan University of Medical Sciences, Semnan, Iran.
Yalda YazdaniImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Amir Salek FarrokhiDepartment of Immunology, Pasteur Institute, Tehran, Iran.
Fatemeh GhorbaniDepartment of Immunology, Semnan University of Medical Sciences, Semnan, Iran.
Mohammadhossein TaherianStudent Research Committee, Semnan University of Medical Sciences, Semnan, Iran.
Bahman YousefiCancer Research Center, Semnan University of Medical Sciences, Semnan, Iran. yosefi_bahman@semums.ac.ir.ORCID http://orcid.org/0000-0002-9889-2195
Semnan University of Medical Sciences · IRTabriz University of Medical Sciences · IRPasteur Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chrysin (Chr) has drawn a lot of attention recently due to its possible anticancer properties. However, Chr's short half-life and low bioavailability restricted its utility as a medicinal agent. The purpose of this research is to design, synthesize, and test the cytotoxic effects of nano-niosomes containing chrysin (Chr-Nio) on the SKOV3 ovarian cancer cell line. Chr-Nio has a nanoparticle polydispersity index (PDI) of 0.156 and a zeta potential of - 27.4 mV, with an average diameter of 105 nm. Furthermore, Chr was encapsulated in Nio with an entrapment effectiveness of 85.5%. Chr-Nio cytotoxicity was shown to be more than free Chr in a time- and dose-dependent manner. Furthermore, as compared to free Chr-treated cells, the mRNA expression level of apoptotic genes Bcl-2, Bax, and caspase-3 in Chr-Nio-treated cells was considerably altered. According to the data, Chr may inhibit SKOV3 cell migration in vitro scratch wound experiments in a dose-dependent manner, and cells treated with Chr-Nio had the highest percentage of cell death. The findings of this study suggested that encapsulating Chr in niosome nanoparticles might be an effective medication delivery strategy for increasing Chr anticancer effects in the treatment of ovarian cancer.

Indexed as

NanoparticlesOvarian NeoplasmsCarcinoma, Ovarian EpithelialDrug Delivery SystemsFemaleFlavonoidsHumansLiposomeschrysinFlavonoidsLiposomesChrysinCytotoxic effectsNano-niosomesOvarian cancer

Identifiers

PMID36723692
OpenAlexW4318755292

What OpenQuestion holds

Textmetadata
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.