Evidence map›Paper›PMID 39129390›Full record

ArticleMolecular oncology2025

Inhibition of autophagy as a novel treatment for neurofibromatosis type 1 tumors.

Megan Stevens, Yuanli Wang, Stephanie J Bouley, Torrey R Mandigo, Aditi Sharma, Sonali Sengupta, Amy Housden, Norbert Perrimon, James A Walker, Benjamin E Housden

Erratum issuedAbstract read
In one paragraph

Article in Molecular oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Megan StevensLiving Systems Institute, University of Exeter, UK.
Yuanli WangLiving Systems Institute, University of Exeter, UK.
Stephanie J BouleyCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID https://orcid.org/0000-0003-0785-0860
Torrey R MandigoCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID https://orcid.org/0000-0003-1795-8242
Aditi SharmaCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Sonali SenguptaLiving Systems Institute, University of Exeter, UK.
Amy HousdenLiving Systems Institute, University of Exeter, UK.
Norbert PerrimonDepartment of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
James A WalkerCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID https://orcid.org/0000-0001-5585-698X
Benjamin E HousdenLiving Systems Institute, University of Exeter, UK.ORCID https://orcid.org/0000-0001-9134-4279

Funding

Tuberous Sclerosis-Pathway and PathogenesisP01CA120964 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI David J. Kwiatkowski · 2007 to 2026
$35.9M
Partners Healthcare Training Program in Precision and Genomic MedicineT32HG010464 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI HEIDI L REHM, JORDAN W SMOLLER · 2019 to 2026
$3.1M
Functional analysis of pathogenic mutations in Neurofibromatosis Type-1 (NF1)R21NS096402 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI WALKER, JAMES ANTHONY · 2016 to 2017
$465k
Congressionally Directed Medical Research Programs NFRP EIRA HT9425-23-1-0831Congressionally Directed Medical Research Programs NFRP W81XWH-16-1-0220Medical Research Council MC_PC_19037Medical Research Council MR/V009583/1NCI NIH HHS P01 CA120964NHGRI NIH HHS T32 HG010464NIH HHS R21 NS096402NINDS NIH HHS R21 NS096402Wellcome Trust
6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is a genetic disorder caused by mutation of the NF1 gene that is associated with various symptoms, including the formation of benign tumors, called neurofibromas, within nerves. Drug treatments are currently limited. The mitogen-activated protein kinase kinase (MEK) inhibitor selumetinib is used for a subset of plexiform neurofibromas (PNs) but is not always effective and can cause side effects. Therefore, there is a clear need to discover new drugs to target NF1-deficient tumor cells. Using a Drosophila cell model of NF1, we performed synthetic lethal screens to identify novel drug targets. We identified 54 gene candidates, which were validated with variable dose analysis as a secondary screen. Pathways associated with five candidates could be targeted using existing drugs. Among these, chloroquine (CQ) and bafilomycin A1, known to target the autophagy pathway, showed the greatest potential for selectively killing NF1-deficient Drosophila cells. When further investigating autophagy-related genes, we found that 14 out of 30 genes tested had a synthetic lethal interaction with NF1. These 14 genes are involved in multiple aspects of the autophagy pathway and can be targeted with additional drugs that mediate the autophagy pathway, although CQ was the most effective. The lethal effect of autophagy inhibitors was conserved in a panel of human NF1-deficient Schwann cell lines, highlighting their translational potential. The effect of CQ was also conserved in a Drosophila NF1 in vivo model and in a xenografted NF1-deficient tumor cell line grown in mice, with CQ treatment resulting in a more significant reduction in tumor growth than selumetinib treatment. Furthermore, combined treatment with CQ and selumetinib resulted in a further reduction in NF1-deficient cell viability. In conclusion, NF1-deficient cells are vulnerable to disruption of the autophagy pathway. This pathway represents a promising target for the treatment of NF1-associated tumors, and we identified CQ as a candidate drug for the treatment of NF1 tumors.

Indexed as

AutophagyNeurofibromatosis 1AnimalsCell Line, TumorChloroquineDrosophila melanogasterHumansMacrolidesMiceNeurofibromin 1bafilomycin A1ChloroquineMacrolidesNeurofibromin 1autophagyDrosophiladrug repurposingneurofibromatosis type 1synthetic lethality

Identifiers

PMID39129390
PMCPMC11887668

What Socratic 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 Socratic graph.