Evidence map›Paper›PMID 35011273›Full record

ReviewMolecules (Basel, Switzerland)2021

Copper(II) Phenanthroline-Based Complexes as Potential AntiCancer Drugs: A Walkthrough on the Mechanisms of Action.

Sebastiano Masuri, Petr Vaňhara, Maria Grazia Cabiddu, Lukáš Moráň, Josef Havel, Enzo Cadoni, Tiziana Pivetta

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.9field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  7. Review
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  13. The Anti-Pathogens (Basel, Switzerland) · 2023
    Article
  14. Review
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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

7 authors at 2 institutions in 2 countries.

Sebastiano MasuriDepartment of Chemical and Geological Sciences, University of Cagliari, 09042 Cagliari, Italy.ORCID 0000-0001-8913-6251
Petr VaňharaDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Maria Grazia CabidduDepartment of Chemical and Geological Sciences, University of Cagliari, 09042 Cagliari, Italy.ORCID 0000-0002-9819-8996
Lukáš MoráňDepartment of Histology and Embryology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic.
Josef HavelInternational Clinical Research Center, St. Anne's University Hospital, 65691 Brno, Czech Republic.
Enzo CadoniDepartment of Chemical and Geological Sciences, University of Cagliari, 09042 Cagliari, Italy.
Tiziana PivettaDepartment of Chemical and Geological Sciences, University of Cagliari, 09042 Cagliari, Italy.
University of Cagliari · ITMasaryk University · CZ

Funding

Masaryk Memorial Cancer Institute 00209805Masaryk University MUNI/A/1390/2020Masaryk University MUNI/A/1689/2020
6 · The paper itself

Abstract

Copper is an endogenous metal ion that has been studied to prepare a new antitumoral agent with less side-effects. Copper is involved as a cofactor in several enzymes, in ROS production, in the promotion of tumor progression, metastasis, and angiogenesis, and has been found at high levels in serum and tissues of several types of human cancers. Under these circumstances, two strategies are commonly followed in the development of novel anticancer Copper-based drugs: the sequestration of free Copper ions and the synthesis of Copper complexes that trigger cell death. The latter strategy has been followed in the last 40 years and many reviews have covered the anticancer properties of a broad spectrum of Copper complexes, showing that the activity of these compounds is often multi factored. In this work, we would like to focus on the anticancer properties of mixed Cu(II) complexes bearing substituted or unsubstituted 1,10-phenanthroline based ligands and different classes of inorganic and organic auxiliary ligands. For each metal complex, information regarding the tested cell lines and the mechanistic studies will be reported and discussed. The exerted action mechanisms were presented according to the auxiliary ligand/s, the metallic centers, and the increasing complexity of the compound structures.

Indexed as

Antineoplastic AgentsCell Line, TumorCell SurvivalChemistry Techniques, SyntheticCoordination ComplexesCopperDose-Response Relationship, DrugHumansInhibitory Concentration 50LigandsMolecular StructurePhenanthrolinesAntineoplastic AgentsCoordination ComplexesCopperLigandsPhenanthrolines1,10-phenanthrolineanticancer chemotherapycancercell stress responsechemoresistancecoordination compoundscopper

Identifiers

PMID35011273
PMCPMC8746828
OpenAlexW4200094046

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.