Evidence map›Paper›PMID 31980698›Full record

ArticleScientific reports2020

Interactions of Cisplatin and Daunorubicin at the Chromatin Level.

Erfaneh Firouzi Niaki, Thibaut Van Acker, László Imre, Péter Nánási, Szabolcs Tarapcsák, Zsolt Bacsó, Frank Vanhaecke, Gábor Szabó

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Topoisomerases inhibition and DNA binding mode of daunomycin-oligoarginine conjugate.Journal of enzyme inhibition and medicinal chemistry · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Erfaneh Firouzi NiakiDepartment of Biophysics and Cell Biology, University of Debrecen, Faculty of Medicine, Debrecen, H-4032, Hungary.
Thibaut Van AckerDepartment of Chemistry, Atomic & Mass Spectrometry - A&MS Research Unit, Ghent University, Campus Sterre, Krijgslaan 281-S12, 9000, Ghent, Belgium.ORCID http://orcid.org/0000-0002-0649-7228
László ImreDepartment of Biophysics and Cell Biology, University of Debrecen, Faculty of Medicine, Debrecen, H-4032, Hungary.
Péter NánásiDepartment of Biophysics and Cell Biology, University of Debrecen, Faculty of Medicine, Debrecen, H-4032, Hungary.
Szabolcs TarapcsákDepartment of Biophysics and Cell Biology, University of Debrecen, Faculty of Medicine, Debrecen, H-4032, Hungary.
Zsolt BacsóDepartment of Biophysics and Cell Biology, University of Debrecen, Faculty of Medicine, Debrecen, H-4032, Hungary.
Frank VanhaeckeDepartment of Chemistry, Atomic & Mass Spectrometry - A&MS Research Unit, Ghent University, Campus Sterre, Krijgslaan 281-S12, 9000, Ghent, Belgium.ORCID http://orcid.org/0000-0002-1884-3853
Gábor SzabóDepartment of Biophysics and Cell Biology, University of Debrecen, Faculty of Medicine, Debrecen, H-4032, Hungary. szabog@med.unideb.hu.
University of Debrecen · HUGhent University · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Unexpectedly, the widely used anticancer agents Cisplatin (Cis-Pt) and Daunorubicin (Dauno) exhibited cell type- and concentration-dependent synergy or antagonism in vitro. We attempted to interpret these effects in terms of the changes elicited by the drugs in the chromatin, the target held primarily responsible for the cytotoxicity of both agents. We measured the effect of Cis-Pt on the levels of Dauno in different cell compartments, the effect of Cis-Pt on Dauno-induced nucleosome eviction, and assessed the influence of Dauno on DNA platination in flow- and laser scanning cytometry as well as in laser ablation-inductively coupled plasma-mass spectrometry assays. We show that the two drugs antagonize each other through a decrease of interstrand crosslinks upon co-treatment with Dauno, and also via the diminished Dauno uptake in the presence of Cis-Pt, and both effects are observed already at low Dauno concentrations. At high Dauno concentrations synergy becomes dominant because histone eviction by Dauno intercalation into the DNA is enhanced in the presence of co-treatment with Cis-Pt. These interactions may have an impact on the efficacy of combination treatment protocols, considering the long retention time of DNA adducts formed by both agents.

Indexed as

Antineoplastic AgentsCell Line, TumorChromatinCisplatinDaunorubicinDNA AdductsDNA, NeoplasmDose-Response Relationship, DrugDrug InteractionsHumansAntineoplastic AgentsChromatinCisplatinDaunorubicinDNA AdductsDNA, Neoplasm

Identifiers

PMID31980698
PMCPMC6981277
OpenAlexW3001803022

What OpenQuestion holds

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LicenceCC BY
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.