Evidence map›Paper›PMID 28205649›Full record

ArticleMetallomics : integrated biometal science2017

Comparative studies of oxaliplatin-based platinum(iv) complexes in different in vitro and in vivo tumor models.

Simone Göschl, Ekaterina Schreiber-Brynzak, Verena Pichler, Klaudia Cseh, Petra Heffeter, Ute Jungwirth, Michael A Jakupec, Walter Berger, Bernhard K Keppler

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Metallomics : integrated biometal science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
  3. Einbau von (Bioaktiven) Äquatorialen Liganden in Platin(IV)-Komplexe.Angewandte Chemie (Weinheim an der Bergstrasse, Germany) · 2023
    Article
  4. Insertion of (Bioactive) Equatorial Ligands into Platinum(IV) Complexes.Angewandte Chemie (International ed. in English) · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Affinities to Oxaliplatin: Vitamins from B Group vs. Nucleobases.International journal of molecular sciences · 2022
    Article
  12. The Pt(International journal of molecular sciences · 2022
    Article
  13. Article
  14. Article
  15. Review
  16. Review
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  18. Review
  19. Article
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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

9 authors at 2 institutions in 2 countries.

Simone GöschlUniversity of Vienna, Institute of Inorganic Chemistry, Waehringer Strasse 42, 1090 Vienna, Austria. michael.jakupec@univie.ac.at.
Ekaterina Schreiber-BrynzakUniversity of Vienna, Institute of Inorganic Chemistry, Waehringer Strasse 42, 1090 Vienna, Austria. michael.jakupec@univie.ac.at.
Verena PichlerUniversity of Vienna, Institute of Inorganic Chemistry, Waehringer Strasse 42, 1090 Vienna, Austria. michael.jakupec@univie.ac.at and University of Vienna, Research Platform "Translational Cancer Therapy Research", Vienna, Austria.
Klaudia CsehUniversity of Vienna, Institute of Inorganic Chemistry, Waehringer Strasse 42, 1090 Vienna, Austria. michael.jakupec@univie.ac.at.
Petra HeffeterUniversity of Vienna, Research Platform "Translational Cancer Therapy Research", Vienna, Austria and Medical University of Vienna, Department of Medicine I, Institute of Cancer Research, Vienna, Austria and Medical University of Vienna, Comprehensive Cancer Center, Vienna, Austria.
Ute JungwirthMedical University of Vienna, Department of Medicine I, Institute of Cancer Research, Vienna, Austria and The Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK.
Michael A JakupecUniversity of Vienna, Institute of Inorganic Chemistry, Waehringer Strasse 42, 1090 Vienna, Austria. michael.jakupec@univie.ac.at and University of Vienna, Research Platform "Translational Cancer Therapy Research", Vienna, Austria.ORCID 0000-0001-7945-1426
Walter BergerUniversity of Vienna, Research Platform "Translational Cancer Therapy Research", Vienna, Austria and Medical University of Vienna, Department of Medicine I, Institute of Cancer Research, Vienna, Austria and Medical University of Vienna, Comprehensive Cancer Center, Vienna, Austria.
Bernhard K KepplerUniversity of Vienna, Institute of Inorganic Chemistry, Waehringer Strasse 42, 1090 Vienna, Austria. michael.jakupec@univie.ac.at and University of Vienna, Research Platform "Translational Cancer Therapy Research", Vienna, Austria.
University of Vienna · ATInstitute of Cancer Research · GB

Funding

Austrian Science Fund FWF P 26603
6 · The paper itself

Abstract

Using platinum(iv) prodrugs of clinically established platinum(ii) compounds is a strategy to overcome side effects and acquired resistances. We studied four oxaliplatin-derived platinum(iv) complexes with varying axial ligands in various in vitro and in vivo settings. The ability to interfere with DNA (pUC19) in the presence and absence of a reducing agent (ascorbic acid) was investigated in cell-free experiments. Cytotoxicity was compared under normoxic and hypoxic conditions in monolayer cultures and multicellular spheroids of colon carcinoma cell lines. Effects on the cell cycle were investigated by flow cytometry, and the capacity of inducing apoptosis was confirmed by flow cytometry and Western blotting. The anti-cancer activity of one complex was studied in vivo in immunodeficient and immunocompetent mice, and the platinum levels in various organs and the tumor after treatment were quantified. The results demonstrate that modification of the axial ligands can improve the cytotoxic potency. The complexes are able to interfere with plasmid DNA, which is enhanced by co-incubation with a reducing agent, and cause cell cycle perturbations. At higher concentrations, they induce apoptosis, but generate only low levels of reactive oxygen species. Two of the complexes increase the life span of leukemia (L1210) bearing mice, and one showed effects similar to oxaliplatin in a CT26 solid tumor model, despite the low platinum levels in the tumor. As in the case of oxaliplatin, activity in the latter model depends on an intact immune system. These findings show new perspectives for the development of platinum(iv) prodrugs of the anticancer agent oxaliplatin, combining bioreductive properties and immunogenic aspects.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell CycleCell ProliferationCisplatinColonic NeoplasmsHumansIn Vitro TechniquesLeukemia L1210MaleMiceMice, Inbred BALB CMice, Inbred DBAMice, SCIDOrganoplatinum CompoundsAntineoplastic AgentsCisplatinOrganoplatinum CompoundsOxaliplatin

Identifiers

PMID28205649
PMCPMC6130776
OpenAlexW2588496926

What OpenQuestion holds

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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.