Evidence map›Paper›PMID 31583820›Full record

ArticleMolecular oncology2019

Antitumor and antiangiogenic activity of the novel chimeric inhibitor animacroxam in testicular germ cell cancer.

Gustav Steinemann, Alexandra Dittmer, Jacob Schmidt, David Josuttis, Michael Fähling, Bernhard Biersack, Nicola Beindorff, Eva Jolante Koziolek, Rainer Schobert, Winfried Brenner and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  7. Article
  8. Review
  9. Epigenetic Regulation of Driver Genes in Testicular Tumorigenesis.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Review
  12. The component of the mJournal of experimental & clinical cancer research : CR · 2021
    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

13 authors at 4 institutions in 1 country.

Gustav SteinemannCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Institute of Physiology, Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.ORCID 0000-0002-4439-3577
Alexandra DittmerCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Institute of Physiology, Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.
Jacob SchmidtCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Institute of Physiology, Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.
David JosuttisCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Institute of Physiology, Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.
Michael FählingCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Institute of Vegetative Physiology, Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.
Bernhard BiersackDepartment of Organic Chemistry, University of Bayreuth, Germany.
Nicola BeindorffCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Berlin Experimental Radionuclide Imaging Center (BERIC), Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.
Eva Jolante KoziolekCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Berlin Experimental Radionuclide Imaging Center (BERIC), Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.
Rainer SchobertDepartment of Organic Chemistry, University of Bayreuth, Germany.
Winfried BrennerCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Berlin Experimental Radionuclide Imaging Center (BERIC), Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.
Thomas MüllerClinic of Internal Medicine IV - Hematology and Oncology Division, Universitätsklinikum Halle (Saale), Germany.
Bianca NitzscheCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Institute of Physiology, Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.ORCID 0000-0001-7916-3344
Michael HöpfnerCorporate Member of Freie Universität Berlin, Berlin Institute of Health, Institute of Physiology, Humboldt-Universität zu Berlin, Charité - Universitätsmedizin Berlin, Germany.
Humboldt-Universität zu Berlin · DEUniversity of Bayreuth · DEGerman Cancer Research Center · DEUniversity Hospital in Halle · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric inhibitors, which merge two drug pharmacophores in a single molecule have become a prominent approach for the design of novel anticancer compounds. Here, we examined animacroxam, which combines histone deacetylase (HDAC) inhibitory and cytoskeleton-interfering pharmacophores, in testicular germ cell tumors (TGCT). The effectiveness of animacroxam was compared to that of the commonly applied chemotherapeutic cisplatin as well as the clinically approved HDAC inhibitor vorinostat. The antineoplastic and antiangiogenic effects of animacroxam on TGCT in vivo were assessed through exploratory animal studies and a modified chorioallantoic membrane assay, revealing that animacroxam has significant antitumor activity in TGCT. A novel positron emission tomography/MR-imaging approach was applied to determine tumor volume and glucose [2-fluoro-2-deoxy-d-glucose (18F-FDG)] uptake in TGCT tumors, revealing reduced glucose uptake in animacroxam-treated TGCTs and showing a dose-dependent suppression of glycolytic enzymes, which led to a breakdown in glycolytic energy production. Furthermore, the observed antiangiogenic effects of animacroxam were related to its ability to inhibit endothelial cell-cell communication, as the expression of gap junction-forming connexin 43 was strongly suppressed, and gap-junctional intercellular mass transport was reduced. Our data suggest that the chimeric HDAC inhibitor animacroxam may become a promising candidate for the treatment of solid cancers and may serve as an interesting alternative to platinum-based therapies.

Indexed as

Neoplasms, Germ Cell and EmbryonalTesticular NeoplasmsAnimalsAntineoplastic AgentsCell Line, TumorCinnamatesHistone Deacetylase InhibitorsHumansImidazolesMaleMiceMice, NudeXenograft Model Antitumor AssaysanimacroxamAntineoplastic AgentsCinnamatesHistone Deacetylase InhibitorsImidazolescancer therapychick chorioallantoic membraneHDAC inhibitorsPET/MR imagingtumor angiogenesis

Identifiers

PMID31583820
PMCPMC6887589
OpenAlexW2978818163

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.