Evidence map›Paper›PMID 31238524›Full record

ArticleProteomes2019

A Proteomic View of Cellular Responses to Anticancer Quinoline-Copper Complexes.

Bastien Dalzon, Joanna Bons, Hélène Diemer, Véronique Collin-Faure, Caroline Marie-Desvergne, Muriel Dubosson, Sarah Cianferani, Christine Carapito, Thierry Rabilloud

Open access · goldAbstract read
In one paragraph

Article in Proteomes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Exploring the Potential of Metal-Based Candidate Drugs as Modulators of the Cytoskeleton.Chembiochem : a European journal of chemical biology · 2023
    Review
  3. Demonstration ofMicrobiology spectrum · 2021
    Article
  4. Review
  5. A Low-Serum Culture System for ProlongedFrontiers in toxicology · 2021
    Review
  6. Article
  7. Article
  8. 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

9 authors at 5 institutions in 1 country.

Bastien DalzonChemistry and Biology of Metals, Univ. Grenoble Alpes, CNRS UMR5249, CEA, IRIG,CBM, F-38054 Grenoble, France. bastien.dalzon@gmail.com.
Joanna BonsLaboratoire de Spectrométrie de Masse BioOrganique (LSMBO), Université de Strasbourg, CNRS, IPHC UMR 7178, 67000 Strasbourg, France. joanna.bons@etu.unistra.fr.
Hélène DiemerLaboratoire de Spectrométrie de Masse BioOrganique (LSMBO), Université de Strasbourg, CNRS, IPHC UMR 7178, 67000 Strasbourg, France. hdiemer@unistra.fr.
Véronique Collin-FaureChemistry and Biology of Metals, Univ. Grenoble Alpes, CNRS UMR5249, CEA, IRIG,CBM, F-38054 Grenoble, France. veronique.collin@cea.fr.
Caroline Marie-DesvergneNanosafety Platform, Medical Biology Laboratory (LBM), Univ. Grenoble-Alpes, CEA, 17 rue des Martyrs, F-38054 Grenoble, France. caroline.desvergne@cea.fr.
Muriel DubossonNanosafety Platform, Medical Biology Laboratory (LBM), Univ. Grenoble-Alpes, CEA, 17 rue des Martyrs, F-38054 Grenoble, France. muriel.dubosson@cea.fr.
Sarah CianferaniLaboratoire de Spectrométrie de Masse BioOrganique (LSMBO), Université de Strasbourg, CNRS, IPHC UMR 7178, 67000 Strasbourg, France. sarah.cianferani@unistra.fr.
Christine CarapitoLaboratoire de Spectrométrie de Masse BioOrganique (LSMBO), Université de Strasbourg, CNRS, IPHC UMR 7178, 67000 Strasbourg, France. ccarapito@unistra.fr.
Thierry RabilloudChemistry and Biology of Metals, Univ. Grenoble Alpes, CNRS UMR5249, CEA, IRIG,CBM, F-38054 Grenoble, France. thierry.rabilloud@cea.fr.
Centre National de la Recherche Scientifique · FRCEA Grenoble · FRUniversité Grenoble Alpes · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRUniversité de Strasbourg · FR

Funding

Agence Nationale de la Recherche ANR-10-INBS-08-03Centre National de la Recherche Scientifique N/AUniversité de Strasbourg N/AUniversité Grenoble Alpes N/A
6 · The paper itself

Abstract

Metal-containing drugs have long been used in anticancer therapies. The mechansims of action of platinum-based drugs are now well-understood, which cannot be said of drugs containing other metals, such as gold or copper. To gain further insights into such mechanisms, we used a classical proteomic approach based on two-dimensional elelctrophoresis to investigate the mechanisms of action of a hydroxyquinoline-copper complex, which shows promising anticancer activities, using the leukemic cell line RAW264.7 as the biological target. Pathway analysis of the modulated proteins highlighted changes in the ubiquitin/proteasome pathway, the mitochondrion, the cell adhesion-cytoskeleton pathway, and carbon metabolism or oxido-reduction. In line with these prteomic-derived hypotheses, targeted validation experiments showed that the hydroxyquinoline-copper complex induces a massive reduction in free glutathione and a strong alteration in the actin cytoskeleton, suggesting a multi-target action of the hydroxyquinoline-copper complex on cancer cells.

Indexed as

actin cytoskeletonanticancer copper complexantioxidant defenseglutathionehydroxyquinoline copper complexleukemic cellsproteasomeproteomicstwo-dimensional electrophoresis

Identifiers

PMID31238524
PMCPMC6630412
OpenAlexW2952666457

What OpenQuestion holds

Textmetadata
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.