Evidence map›Paper›PMID 35511749›Full record

ArticleMolecular cancer therapeutics2022

A High-Throughput Screening Platform Identifies Novel Combination Treatments for Malignant Peripheral Nerve Sheath Tumors.

Juana Fernández-Rodríguez, Edgar Creus-Bachiller, Xiaohu Zhang, Maria Martínez-Iniesta, Sara Ortega-Bertran, Rajarshi Guha, Craig J Thomas, Margaret R Wallace, Cleofe Romagosa, Lourdes Salazar-Huayna and 8 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Triple Combination of MEK, BET, and CDK Inhibitors Significantly Reduces Human Malignant Peripheral Nerve Sheath Tumors in Mouse Models.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. 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

18 authors at 7 institutions in 3 countries.

Juana Fernández-Rodríguez *Hereditary Cancer Program, Catalan Institute of Oncology, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0002-7760-5804
Edgar Creus-Bachiller *Hereditary Cancer Program, Catalan Institute of Oncology, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0001-7134-3164
Xiaohu ZhangDivision of Preclinical Innovation, National Center for Advancing Translational Sciences, NIH, Rockville, Maryland.ORCID 0000-0002-5872-4656
Maria Martínez-IniestaProgram in Molecular Mechanisms and Experimental Therapy in Oncology (Oncobell), IDIBELL, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0001-6252-6671
Sara Ortega-BertranHereditary Cancer Program, Catalan Institute of Oncology, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0003-3371-220X
Rajarshi GuhaDivision of Preclinical Innovation, National Center for Advancing Translational Sciences, NIH, Rockville, Maryland.ORCID 0000-0001-7403-8819
Craig J ThomasDivision of Preclinical Innovation, National Center for Advancing Translational Sciences, NIH, Rockville, Maryland.ORCID 0000-0001-9386-9001
Margaret R WallaceDepartment of Molecular Genetics & Microbiology, University of Florida College of Medicine, Gainesville, Florida.ORCID 0000-0002-5202-8895
Cleofe RomagosaCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), Spain.ORCID 0000-0002-9478-7320
Lourdes Salazar-HuaynaDepartment of Pathology, Vall d'Hebron University Hospital, Barcelona, Spain.ORCID 0000-0002-0303-9707
Karlyne M ReillyPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.ORCID 0000-0001-9109-4409
Jaishri O BlakelyNeurofibromatosis Therapeutic Acceleration Program (NTAP), Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland.ORCID 0000-0002-1049-0993
Jordi Serra-MusachProcure Program, Catalan Institute of Oncology, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0002-5754-6712
Miguel Angel PujanaProgram in Molecular Mechanisms and Experimental Therapy in Oncology (Oncobell), IDIBELL, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0003-3222-4044
Eduard SerraCentro de Investigación Biomédica en Red de Cáncer (CIBERONC), Spain.ORCID 0000-0003-2895-9857
Alberto VillanuevaProgram in Molecular Mechanisms and Experimental Therapy in Oncology (Oncobell), IDIBELL, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0001-5164-0006
Marc FerrerDivision of Preclinical Innovation, National Center for Advancing Translational Sciences, NIH, Rockville, Maryland.ORCID 0000-0003-4569-9137
Conxi LázaroHereditary Cancer Program, Catalan Institute of Oncology, Hospitalet de Llobregat, Barcelona, Spain.ORCID 0000-0002-7198-5906
Institut Català d'Oncologia · ESNational Center for Advancing Translational Sciences · USHebron University · PSInstitut d'Investigació en Ciències de la Salut Germans Trias i Pujol · ESJohns Hopkins University · USNational Cancer Institute · USUniversity of Florida · US

Funding

Molecular, Cellular and Genetic Analyses of Malignancies Associated with NF1ZIABC011754 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI REILLY, KARLYNE M · 2017 to 2025
$6.4M
Novel small molecule library developmentZIATR000043 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI THOMAS, CRAIG · 2015 to 2025
$3.3M
Intramural NIH HHS Z99 TR999999
6 · The paper itself

Abstract

Malignant peripheral nerve sheath tumors (MPNST) are soft-tissue sarcomas that are the leading cause of mortality in patients with Neurofibromatosis type 1 (NF1). Single chemotherapeutic agents have shown response rates ranging from 18% to 44% in clinical trials, so there is still a high medical need to identify chemotherapeutic combination treatments that improve clinical prognosis and outcome. We screened a collection of compounds from the NCATS Mechanism Interrogation PlatE (MIPE) library in three MPNST cell lines, using cell viability and apoptosis assays. We then tested whether compounds that were active as single agents were synergistic when screened as pairwise combinations. Synergistic combinations in vitro were further evaluated in patient-derived orthotopic xenograft/orthoxenograft (PDOX) athymic models engrafted with primary MPNST matching with their paired primary-derived cell line where synergism was observed. The high-throughput screening identified 21 synergistic combinations, from which four exhibited potent synergies in a broad panel of MPNST cell lines. One of the combinations, MK-1775 with Doxorubicin, significantly reduced tumor growth in a sporadic PDOX model (MPNST-SP-01; sevenfold) and in an NF1-PDOX model (MPNST-NF1-09; fourfold) and presented greater effects in TP53 mutated MPNST cell lines. The other three combinations, all involving Panobinostat (combined with NVP-BGT226, Torin 2, or Carfilzomib), did not reduce the tumor volume in vivo at noncytotoxic doses. Our results support the utility of our screening platform of in vitro and in vivo models to explore new therapeutic approaches for MPNSTs and identified that combination MK-1775 with Doxorubicin could be a good pharmacologic option for the treatment of these tumors.

Indexed as

Nerve Sheath NeoplasmsNeurofibromatosis 1NeurofibrosarcomaCell Line, TumorDoxorubicinHigh-Throughput Screening AssaysHumansDoxorubicin

Identifiers

PMID35511749
PMCPMC9256801
OpenAlexW4229003041

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.