Evidence map›Paper›PMID 33743824›Full record

ArticleCell & bioscience2021

Cooperative treatment effectiveness of ATR and HSP90 inhibition in Ewing's sarcoma cells.

Christian Marx, Marc U Schaarschmidt, Joanna Kirkpatrick, Lisa Marx-Blümel, Melisa Halilovic, Martin Westermann, Doerte Hoelzer, Felix B Meyer, Yibo Geng, Katrin Buder and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. TH-302 (evofosfamide) monotherapy exerts anticancer activity in Ewing's sarcoma cells under hypoxia.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Assessment of HDAC Inhibitor-Induced Endoplasmic Reticulum (ER) Stress.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  12. Review
  13. Cancers · 2022
    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

17 authors at 7 institutions in 3 countries.

Christian MarxLeibniz Institute On Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Marc U SchaarschmidtDepartment of Pediatric Hematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
Joanna KirkpatrickLeibniz Institute On Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Lisa Marx-BlümelDepartment of Pediatric Hematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
Melisa HalilovicLeibniz Institute On Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Martin WestermannElectron Microscopy Center, Jena University Hospital, Jena, Germany.
Doerte HoelzerDepartment of Human Nutrition, Institute of Nutrition, Friedrich Schiller University Jena, Jena, Germany.
Felix B MeyerDepartment of Human Nutrition, Institute of Nutrition, Friedrich Schiller University Jena, Jena, Germany.
Yibo GengLeibniz Institute On Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Katrin BuderLeibniz Institute On Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Hauke M SchadwinkelDepartment of Pediatric Hematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
Kanstantsin SiniukLeibniz Institute On Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Sabine BeckerDepartment of Pediatric Hematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
René ThierbachDepartment of Human Nutrition, Institute of Nutrition, Friedrich Schiller University Jena, Jena, Germany.
James F BeckDepartment of Pediatric Hematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany.
Jürgen Sonnemann *Department of Pediatric Hematology and Oncology, Children's Clinic, Jena University Hospital, Jena, Germany. juergen.sonnemann@med.uni-jena.de.ORCID http://orcid.org/0000-0003-2993-9161
Zhao-Qi Wang *Leibniz Institute On Aging - Fritz Lipmann Institute (FLI), Jena, Germany.
Jena University Hospital · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEFriedrich Schiller University Jena · DEBioNTech (Germany) · DECapital Medical University · CNKlinik und Poliklinik für Kinder- und Jugendmedizin · DEThe Francis Crick Institute · GB

Funding

DFG WA2627/1-1DFG WA2627/5-1German-Israeli Foundation for Scientific Research and Development I-1307-418.13/2015Leibniz-Gemeinschaft SAW2014Leibniz-Gemeinschaft SAW2015
6 · The paper itself

Abstract

introductionEwing's sarcoma is an aggressive childhood malignancy whose outcome has not substantially improved over the last two decades. In this study, combination treatments of the HSP90 inhibitor AUY922 with either the ATR inhibitor VE821 or the ATM inhibitor KU55933 were investigated for their effectiveness in Ewing's sarcoma cells.

methodsEffects were determined in p53 wild-type and p53 null Ewing's sarcoma cell lines by flow cytometric analyses of cell death, mitochondrial depolarization and cell-cycle distribution as well as fluorescence and transmission electron microscopy. They were molecularly characterized by gene and protein expression profiling, and by quantitative whole proteome analysis.

resultsAUY922 alone induced DNA damage, apoptosis and ER stress, while reducing the abundance of DNA repair proteins. The combination of AUY922 with VE821 led to strong apoptosis induction independent of the cellular p53 status, yet based on different molecular mechanisms. p53 wild-type cells activated pro-apoptotic gene transcription and underwent mitochondria-mediated apoptosis, while p53 null cells accumulated higher levels of DNA damage, ER stress and autophagy, eventually leading to apoptosis. Impaired PI3K/AKT/mTOR signaling further contributed to the antineoplastic combination effects of AUY922 and VE821. In contrast, the combination of AUY922 with KU55933 did not produce a cooperative effect.

conclusionOur study reveals that HSP90 and ATR inhibitor combination treatment may be an effective therapeutic approach for Ewing's sarcoma irrespective of the p53 status.

Indexed as

ApoptosisATMATREndoplasmic reticulum (ER) stressEwing's sarcomaHSP90

Identifiers

PMID33743824
PMCPMC7981928
OpenAlexW3114373975

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.