Evidence map›Paper›PMID 36139615›Full record

ArticleCancers2022

Thiosemicarbazone Derivatives Developed to Overcome COTI-2 Resistance.

Vivien Pósa, Alessia Stefanelli, Julia H Bormio Nunes, Sonja Hager, Marlene Mathuber, Nóra V May, Walter Berger, Bernhard K Keppler, Christian R Kowol, Éva A Enyedy and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. ABCC1 promotes GSH-dependent iron transport and resistance to Fe(II) and Cu(II) chelators.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Human serum albumin as a copper source for anticancer thiosemicarbazones.Metallomics : integrated biometal science · 2023
    Article
  9. Article
  10. Review
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 at 4 institutions in 3 countries.

Vivien PósaDepartment of Inorganic and Analytical Chemistry, Interdisciplinary Excellence Centre and MTA-SZTE Lendület Functional Metal Complexes Research Group, University of Szeged, Dóm tér 7, H-6720 Szeged, Hungary.
Alessia StefanelliCenter for Cancer Research, Medical University of Vienna, Borschkegasse 8a, 1090 Vienna, Austria.
Julia H Bormio NunesInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Waehringer Strasse 42, 1090 Vienna, Austria.ORCID 0000-0001-8113-6679
Sonja HagerCenter for Cancer Research, Medical University of Vienna, Borschkegasse 8a, 1090 Vienna, Austria.ORCID 0000-0001-8221-1044
Marlene MathuberInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Waehringer Strasse 42, 1090 Vienna, Austria.
Nóra V MayCentre for Structural Science, Research Centre for Natural Sciences, Magyar Tudósok Körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0003-4770-4681
Walter BergerCenter for Cancer Research, Medical University of Vienna, Borschkegasse 8a, 1090 Vienna, Austria.ORCID 0000-0003-0014-1658
Bernhard K KepplerInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Waehringer Strasse 42, 1090 Vienna, Austria.
Christian R KowolInstitute of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, Waehringer Strasse 42, 1090 Vienna, Austria.ORCID 0000-0002-8311-1632
Éva A EnyedyDepartment of Inorganic and Analytical Chemistry, Interdisciplinary Excellence Centre and MTA-SZTE Lendület Functional Metal Complexes Research Group, University of Szeged, Dóm tér 7, H-6720 Szeged, Hungary.ORCID 0000-0002-8058-8128
Petra HeffeterCenter for Cancer Research, Medical University of Vienna, Borschkegasse 8a, 1090 Vienna, Austria.ORCID 0000-0001-6401-8646
Medical University of Vienna · ATUniversity of Vienna · ATUniversity of Szeged · HUHUN-REN Research Centre for Natural Sciences · HU

Funding

Austrian Agency for International Cooperation in Education and Research HU 02/2020Austrian-Hungarian Scientific & Technological Cooperation 2019-2.1.11-TÉT-2019-00003Austrian Science Fund FWF DOC 59Austrian Science Fund FWF P 31923FWF Austrian Science Fund P31923National Research Development and Innovation Office-NKFIA K 124544New National Excellence Program UNKP-21-3-SZTE-455
6 · The paper itself

Abstract

COTI-2 is currently being evaluated in a phase I clinical trial for the treatment of gynecological and other solid cancers. As a thiosemicarbazone, this compound contains an N,N,S-chelating moiety and is, therefore, expected to bind endogenous metal ions. However, besides zinc, the metal interaction properties of COTI-2 have not been investigated in detail so far. This is unexpected, as we have recently shown that COTI-2 forms stable ternary complexes with copper and glutathione, which renders this drug a substrate for the resistance efflux transporter ABCC1. Herein, the complex formation of COTI-2, two novel terminal N-disubstituted derivatives (COTI-NMe

Indexed as

anticancercopperCOTI-2ironmetal bindingp53resistancestability constantsthiosemicarbazoneszinc

Identifiers

PMID36139615
PMCPMC9497102
OpenAlexW4295796310

What OpenQuestion holds

Textmetadata
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.