Evidence map›Paper›PMID 34779147›Full record

ArticleChemMedChem2022

Investigating Alkylated Prodigiosenes and Their Cu(II)-Dependent Biological Activity: Interactions with DNA, Antimicrobial and Photoinduced Anticancer Activity.

Sebastian Doniz Kettenmann, Matthew White, Julien Colard-Thomas, Matilda Kraft, Andrea T Feßler, Karin Danz, Gerhard Wieland, Sylvia Wagner, Stefan Schwarz, Arno Wiehe and 1 more

Abstract read
In one paragraph

Article in ChemMedChem, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

11 authors.

Sebastian Doniz KettenmannInstitut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstr. 34/36, 14195, Berlin, Germany.
Matthew WhiteInstitut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstr. 34/36, 14195, Berlin, Germany.ORCID 0000-0003-0923-974X
Julien Colard-ThomasInstitut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstr. 34/36, 14195, Berlin, Germany.
Matilda KraftInstitut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstr. 34/36, 14195, Berlin, Germany.
Andrea T FeßlerInstitut für Mikrobiologie und Tierseuchen, Freie Universität Berlin, Robert-von-Ostertag-Str. 7, 14163 Berlin, Germany.ORCID 0000-0002-0510-7347
Karin DanzFraunhofer-Institut für Biomedizinische Technik IBMT, Joseph-von-Fraunhofer-Weg 1, 66280, Sulzbach, Germany.
Gerhard Wielandbiolitec research GmbH, Otto-Schott-Str. 15, 07745, Jena, Germany.ORCID 0000-0003-1034-4897
Sylvia WagnerFraunhofer-Institut für Biomedizinische Technik IBMT, Joseph-von-Fraunhofer-Weg 1, 66280, Sulzbach, Germany.ORCID 0000-0001-7922-977X
Stefan SchwarzInstitut für Mikrobiologie und Tierseuchen, Freie Universität Berlin, Robert-von-Ostertag-Str. 7, 14163 Berlin, Germany.ORCID 0000-0002-6303-8212
Arno Wiehebiolitec research GmbH, Otto-Schott-Str. 15, 07745, Jena, Germany.ORCID 0000-0002-6289-7672
Nora KulakInstitut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstr. 34/36, 14195, Berlin, Germany.ORCID 0000-0002-8347-4046

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prodigiosenes are a family of red pigments with versatile biological activity. Their tripyrrolic core structure has been modified many times in order to manipulate the spectrum of activity. We have been looking systematically at prodigiosenes substituted at the C ring with alkyl chains of different lengths, in order to assess the relevance of this substituent in a context that has not been investigated before for these derivatives: Cu(II) complexation, DNA binding, self-activated DNA cleavage, photoinduced cytotoxicity and antimicrobial activity. Our results indicate that the hydrophobic substituent has a clear influence on the different aspects of their biological activity. The cytotoxicity study of the Cu(II) complexes of these prodigiosenes shows that they exhibit a strong cytotoxic effect towards the tested tumor cell lines. The Cu(II) complex of a prodigiosene lacking any alkyl chain excelled in its photoinduced anticancer activity, thus demonstrating the potential of prodigiosenes and their metal complexes for an application in photodynamic therapy (PDT). Two derivatives along with their Cu(II) complexes showed also antimicrobial activity against Staphylococcus aureus strains.

Indexed as

AlkylationAnimalsAnti-Bacterial AgentsAntineoplastic AgentsCell LineCell ProliferationCell SurvivalCoordination ComplexesCopperDNADNA CleavageDose-Response Relationship, DrugDrug Screening Assays, AntitumorEnterococcus hiraeEscherichia coliHumansAnti-Bacterial AgentsAntineoplastic AgentsCoordination ComplexesCopperDNAReactive Oxygen Speciesantimicrobial agentCu(II) complexescytotoxicityDNA cleavageprodigiosenes

Identifiers

PMID34779147
PMCPMC9306646

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Registered trials

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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.