Evidence map›Paper›PMID 30123424›Full record

ArticleOncotarget2018

Identifying the druggable interactome of EWS-FLI1 reveals MCL-1 dependent differential sensitivities of Ewing sarcoma cells to apoptosis inducers.

Kalliopi Tsafou, Anna Maria Katschnig, Branka Radic-Sarikas, Cornelia Noëlle Mutz, Kristiina Iljin, Raphaela Schwentner, Maximilian O Kauer, Karin Mühlbacher, Dave N T Aryee, David Westergaard and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Ewing sarcoma from molecular biology to the clinic.Frontiers in cell and developmental biology · 2023
    Review
  5. Article
  6. Review
  7. Systems Biology Analysis for Ewing Sarcoma.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  8. Review
  9. 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

16 authors at 6 institutions in 4 countries.

Kalliopi TsafouDisease Systems Biology, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Anna Maria KatschnigChildren's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Branka Radic-SarikasCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Cornelia Noëlle MutzChildren's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Kristiina IljinMedical Biotechnology, VTT Technical Research Centre of Finland, Espoo, Finland.
Raphaela SchwentnerChildren's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Maximilian O KauerChildren's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Karin MühlbacherChildren's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
Dave N T AryeeChildren's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
David WestergaardDisease Systems Biology, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Saija Haapa-PaananenMedical Biotechnology, VTT Technical Research Centre of Finland, Espoo, Finland.
Vidal FeyMedical Biotechnology, VTT Technical Research Centre of Finland, Espoo, Finland.
Giulio Superti-FurgaCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Jeffrey ToretskyDepartment of Oncology, Georgetown University, Medical Center, Washington, DC, USA.
Søren BrunakDisease Systems Biology, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Heinrich KovarChildren's Cancer Research Institute, St. Anna Kinderkrebsforschung, Vienna, Austria.
St Anna Children's Hospital · ATNovo Nordisk Foundation · DKSt. Anna Children's Cancer Research InstituteVTT Technical Research Centre of Finland · FICeMM Research Center for Molecular Medicine · ATGeorgetown University Medical Center · US

Funding

Austrian Science Fund FWF I 1225
6 · The paper itself

Abstract

Ewing sarcoma (EwS) is an aggressive pediatric bone cancer in need of more effective therapies than currently available. Most research into novel targeted therapeutic approaches is focused on the fusion oncogene

Indexed as

apoptosisBCL-2 inhibitorsdrug-target networkEwing sarcomahigh-throughput compound screening

Identifiers

PMID30123424
PMCPMC6089552
OpenAlexW2883145844

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.