Evidence map›Paper›PMID 39770404›Full record

ArticlePharmaceuticals (Basel, Switzerland)2024

mTOR Pathway Inhibition, Anticancer Activity and In Silico Calculations of Novel Hydrazone Derivatives in Two- and Three-Dimensional Cultured Type 1 Endometrial Cancer Cells.

Muhammet Volkan Bulbul, Arif Mermer, Bircan Kolbasi, Fatih Kocabas, Semiha Mervenur Kalender, Kiymet Asli Kirectepe Aydin, Turan Demircan, İlknur Keskin

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 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. 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.

Muhammet Volkan BulbulDepartment of Histology and Embryology, School of Medicine, Agri Ibrahim Cecen University, Agri 04000, Turkey.ORCID 0000-0003-1526-2065
Arif MermerDepartment of Biotechnology, University of Health Sciences, Istanbul 34668, Turkey.
Bircan KolbasiDepartment of Histology and Embryology, School of Medicine, Istanbul Medipol University, Istanbul 34810, Turkey.
Fatih KocabasDepartment of Genetics and Bioengineering, Faculty of Engineering, Yeditepe University, Istanbul 34755, Turkey.
Semiha Mervenur KalenderDepartment of Histology and Embryology, School of Medicine, Istanbul Medipol University, Istanbul 34810, Turkey.ORCID 0000-0002-0885-3417
Kiymet Asli Kirectepe AydinDepartment of Medical Biology and Genetics, Faculty of Medicine, Istanbul Nisantasi University, Istanbul 34398, Turkey.ORCID 0000-0001-8289-5191
Turan DemircanDepartment of Medical Biology, School of Medicine, Mugla Sitki Kocman University, Mugla 48000, Turkey.
İlknur KeskinDepartment of Histology and Embryology, School of Medicine, Istanbul Medipol University, Istanbul 34810, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndometrial cancer remains a significant health concern, with type 1 endometrial cancer characterized by aberrant expression of estrogen-dependent and mTOR pathway proteins. In this study, we evaluated the effects of two novel hydrazone derivatives against the Ishikawa cell line, a model for endometrial cancer.

methodsTwo novel hydrazone derivatives, MVB1 and MVB2, were synthesized and characterized. The anticancer activity of the compounds in both two- and three-dimensional cultured Ishikawa cells was evaluated by MTT assay. The interaction of the compounds with proteins in the PI3K/AKT/mTOR pathway was evaluated by molecular docking studies and in vitro western blot analyses were performed. Additionally, ADME/T calculations were performed to evaluate the drug-like properties of the compounds.

resultsMVB1 and MVB2 showed promising anticancer activity with IC

conclusionsThe findings suggest that MVB1 and MVB2, especially MVB1, are promising candidates for further development as potential therapeutics for endometrial cancer by targeting the PI3K/AKT/mTOR pathway.

Indexed as

endometrial cancerhydrazonemolecular dockingmTORspheroid

Identifiers

PMID39770404
PMCPMC11678851

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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.