Evidence map›Paper›PMID 41036607›Full record

ArticleMolecular cancer therapeutics2026

Pharmacogenomic Synthetic Lethal Screens Reveal Hidden Vulnerabilities and New Therapeutic Approaches for Treatment of NF1-Associated Tumors.

Kyle B Williams, Alex T Larsson, Bryant J Keller, Katherine E Chaney, Rory L Williams, Minu M Bhunia, Garrett M Draper, Tyler A Jubenville, Wendy A Hudson, Gunda I Georg and 3 more

Abstract read
In one paragraph

Article in Molecular cancer therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Kyle B WilliamsDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0003-4333-9111
Alex T LarssonDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-1350-8271
Bryant J KellerDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Katherine E ChaneyDivision of Experimental Hematology and Cancer Biology, Department of Pediatrics, Cincinnati Children's Hospital, University of Cincinnati College of Medicine, Cincinnati, Ohio.ORCID 0000-0001-5485-2821
Rory L WilliamsDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0003-2605-5790
Minu M BhuniaDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-2849-1572
Garrett M DraperDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-4972-8233
Tyler A JubenvilleDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0009-0003-9578-4847
Wendy A HudsonDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0009-0007-7977-3549
Gunda I GeorgDepartment of Medicinal Chemistry, University of Minnesota College of Pharmacy, Minneapolis, Minnesota.ORCID 0000-0002-8900-9460
Christopher L MoertelDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-5474-588X
Nancy RatnerDivision of Experimental Hematology and Cancer Biology, Department of Pediatrics, Cincinnati Children's Hospital, University of Cincinnati College of Medicine, Cincinnati, Ohio.ORCID 0000-0001-5030-9354
David A LargaespadaDepartment of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-3183-0491

Funding

TRAINING GRANT IN MICROBIOLOGY/CANCER RESEARCHT32CA009138 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Scott M. Dehm · 1985 to 2026
$11.3M
Uncovering treatment targets for peripheral nerve sheath tumor progression in NF1R01NS115438 · NINDS · UNIVERSITY OF MINNESOTA · PI LARGAESPADA, DAVID ANDREW, RATNER, NANCY · 2020 to 2024
$2.9M
Disordered Regulation of Wnt/beta-catenin Signaling in MPNST Development and MaintenanceR01NS086219 · NINDS · UNIVERSITY OF MINNESOTA · PI LARGAESPADA, DAVID ANDREW, RATNER, NANCY · 2014 to 2018
$2.4M
Recurrent Tumor-Specific Alternately Processed Transcripts as a Source of Neoantigens for NF1-associated Malignant Peripheral Nerve Sheath Tumor ImmunopreventionUH3CA244687 · NCI · UNIVERSITY OF MINNESOTA · PI LARGAESPADA, DAVID ANDREW · 2021 to 2023
$2.1M
American Cancer Society (ACS) 123939Boston Children's Hospital (BCH) Pre-Clinical Research Award Neurofibromatosis Researach Initiative GENFD0001769008Children's Cancer Research Fund (CCRF) Emerging ScientistChildren's Tumor Foundation (CTF) 2015-18-003AChildren's Tumor Foundation (CTF) 2017-01-021National Cancer Institute (NCI) R01NS086219National Institute of Neurological Disorders and Stroke (NINDS) R01NS115438National Institutes of Health (NIH) 5T32CA009138-40NCI NIH HHS T32 CA009138NCI NIH HHS UH3 CA244687NINDS NIH HHS R01 NS086219NINDS NIH HHS R01 NS115438
6 · The paper itself

Abstract

Neurofibromatosis type I (NF1) is a common cancer predisposition syndrome caused by heterozygous loss-of-function mutations in the tumor-suppressor gene NF1. Individuals with NF1 develop benign tumors of the peripheral nervous system (neurofibromas), originating from the Schwann cell (SC) lineage after somatic loss of the wild-type NF1 allele, some of which progress further to malignant peripheral nerve sheath tumors (MPNST). There is only one FDA-approved targeted therapy for symptomatic plexiform neurofibromas and none approved for MPNSTs. The genetic basis of NF1 syndrome makes associated tumors ideal for using synthetic drug sensitivity approaches to uncover therapeutic vulnerabilities. We developed a drug discovery pipeline to identify therapeutics for NF1-related tumors using isogeneic pairs of NF1-proficient and NF1-deficient immortalized human SCs. We utilized these in a large-scale high-throughput screen for drugs that preferentially kill NF1-deficient cells, through which we identified 23 compounds capable of killing NF1-deficient SCs with selectivity. Multiple hits from this screen clustered into classes defined by the method of action. Four clinically interesting drugs from these classes were tested in vivo using both a genetically engineered mouse model of high-grade PNSTs and human MPNST xenografts. All drugs tested showed single-agent efficacy in these models as well as significant synergy when used in combination with the MEK inhibitor selumetinib. This high-throughput screen platform yielded novel therapeutically relevant compounds for the treatment of NF1-associated tumors and can serve as a tool to rapidly evaluate new compounds and combinations in the future.

Indexed as

Antineoplastic AgentsNeurofibromatosis 1Neurofibromin 1PharmacogeneticsSynthetic Lethal MutationsAnimalsCell Line, TumorDisease Models, AnimalHigh-Throughput Screening AssaysHumansMiceSchwann CellsXenograft Model Antitumor AssaysAntineoplastic AgentsNeurofibromin 1

Identifiers

PMID41036607
PMCPMC12668261

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.