Evidence map›Paper›PMID 36345785›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2023

Identification of the first-in-class dual inhibitors of human DNA topoisomerase IIα and indoleamine-2,3-dioxygenase 1 (IDO 1) with strong anticancer properties.

Barbara Kaproń, Anita Płazińska, Wojciech Płaziński, Tomasz Plech

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2023. 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
0.6field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Rhenium-186-labeledRSC advances · 2026
    Article
  2. CXCR4/CXCL12 blockade therapy; a new horizon in TNBC therapy.Medical oncology (Northwood, London, England) · 2025
    Review
  3. Review
  4. Article
  5. 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

4 authors at 1 institution in 1 country.

Barbara KaprońDepartment of Clinical Genetics, Medical University of Lublin, Lublin, Poland.ORCID 0000-0002-7520-3238
Anita PłazińskaDepartment of Biopharmacy, Medical University of Lublin, Lublin, Poland.
Wojciech PłazińskiDepartment of Biopharmacy, Medical University of Lublin, Lublin, Poland.
Tomasz PlechDepartment of Pharmacology, Medical University of Lublin, Lublin, Poland.ORCID 0000-0002-8162-8435
Medical University of Lublin · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular docking of a large set of thiosemicarbazide-based ligands resulted in obtaining compounds that inhibited both human DNA topoisomerase IIα and indoleamine-2,3-dioxygenase-1 (IDO1). To the best of our knowledge, these compounds are the first dual inhibitors targeting these two enzymes. As both of them participate in the anticancer response, the effect of the compounds on a panel of cancer cell lines was examined. Among the cell lines tested, lung cancer (A549) and melanoma (A375) cells were the most sensitive to compounds

Indexed as

Antineoplastic AgentsNeoplasmsDNA Topoisomerases, Type IIHumansIndoleamine-Pyrrole 2,3,-DioxygenaseLigandsMolecular Docking SimulationSemicarbazidesStructure-Activity RelationshipTopoisomerase II InhibitorsTryptophan OxygenaseAntineoplastic AgentsDNA Topoisomerases, Type IIIndoleamine-Pyrrole 2,3,-DioxygenaseLigandsSemicarbazidesthiosemicarbazideTopoisomerase II InhibitorsTryptophan OxygenaseAntiproliferative activitydocking simulationsimmunotherapythiosemicarbazide derivatives

Identifiers

PMID36345785
PMCPMC9648375
OpenAlexW4308589016

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.