Evidence map›Paper›PMID 36337968›Full record

ArticleRSC advances2022

Synthesis, characterization, antitumor potential, and investigation of mechanism of action of copper(ii) complexes with acylpyruvates as ligands: interactions with biomolecules and kinetic study.

Nenad Joksimović, Jelena Petronijević, Snežana Radisavljević, Biljana Petrović, Kristina Mihajlović, Nenad Janković, Emilija Milović, Dušan Milivojević, Bojana Ilić, Ana Djurić

Abstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Nenad JoksimovićUniversity of Kragujevac, Faculty of Science, Department of Chemistry Radoja Domanovića 12 34000 Kragujevac Serbia nenad.joksimovic@pmf.kg.ac.rs.ORCID https://orcid.org/0000-0003-3365-6762
Jelena PetronijevićUniversity of Kragujevac, Faculty of Science, Department of Chemistry Radoja Domanovića 12 34000 Kragujevac Serbia nenad.joksimovic@pmf.kg.ac.rs.
Snežana RadisavljevićUniversity of Kragujevac, Faculty of Science, Department of Chemistry Radoja Domanovića 12 34000 Kragujevac Serbia nenad.joksimovic@pmf.kg.ac.rs.
Biljana PetrovićUniversity of Kragujevac, Faculty of Science, Department of Chemistry Radoja Domanovića 12 34000 Kragujevac Serbia nenad.joksimovic@pmf.kg.ac.rs.ORCID https://orcid.org/0000-0001-7914-6026
Kristina MihajlovićUniversity of Kragujevac, Faculty of Science, Department of Chemistry Radoja Domanovića 12 34000 Kragujevac Serbia nenad.joksimovic@pmf.kg.ac.rs.
Nenad JankovićUniversity of Kragujevac, Institute for Information Technologies Kragujevac, Department of Sciences Jovana Cvijića bb 34000 Kragujevac Serbia.ORCID https://orcid.org/0000-0002-2295-9410
Emilija MilovićUniversity of Kragujevac, Institute for Information Technologies Kragujevac, Department of Sciences Jovana Cvijića bb 34000 Kragujevac Serbia.
Dušan MilivojevićVinča Institute of Nuclear Science University of Belgrade P.O. Box 522 11001 Belgrade Serbia.
Bojana IlićClinic for Endocrinology, Diabetes and Metabolic Diseases, University Clinical Centre of Serbia Belgrade Serbia.ORCID https://orcid.org/0000-0002-8249-5494
Ana DjurićInstitute of Oncology and Radiology of Serbia Pasterova 14 11000 Belgrade Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Considering the urgency of finding a cure for vicious diseases such as tumors, we have synthesized and characterized a small series of new copper(ii) complexes with biologically important ligands such as acylpyruvate. In addition to this, we used another four copper(ii) complexes, with ligands of the same type to examine the antitumor potential. The antitumor potential of the copper(ii) complexes was examined on three tumor cell lines and one normal human cell line using the MTT assay. All seven tested complexes showed very good cytotoxic effects. Two copper complexes that showed the best antitumor potential were selected for further testing that showed the best potential for potential application in the future. The mechanism of activity of these complexes was examined in detail using tests such as cell cycle, ROS level, oxidative DNA damage, and proteins related to hypoxia analysis. In addition, we examined the binding abilities of these complexes with biomolecules (Guo, Ino, 5'-GMP, BSA, and DNA). The results showed that the tested compounds bind strongly to DNA molecules through intercalation. Also, it has been shown that the tested compounds adequately bind to the BSA molecule, which indicates an even greater potential for some future application of these compounds in clinical practice.

Identifiers

PMID36337968
PMCPMC9597287

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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.