Evidence map›Paper›PMID 30335132›Full record

ArticleHuman molecular genetics2019

A proteasome-resistant fragment of NIK mediates oncogenic NF-κB signaling in schwannomas.

Jeffrey R Gehlhausen, Eric Hawley, Benjamin Mark Wahle, Yongzheng He, Donna Edwards, Steven D Rhodes, Jacquelyn D Lajiness, Karl Staser, Shi Chen, Xianlin Yang and 14 more

Open access · bronzeAbstract read
In one paragraph

Article in Human molecular genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. A Review of Drug Therapy in Vestibular Schwannoma.Drug design, development and therapy · 2021
    Review
  4. Review
  5. 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

24 authors at 5 institutions in 1 country.

Jeffrey R GehlhausenHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Eric HawleyHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Benjamin Mark WahleHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Yongzheng HeHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Donna EdwardsHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Steven D RhodesHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Jacquelyn D LajinessHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Karl StaserDepartment of Medicine, Division of Dermatology, Washington University in Saint Louis, St. Louis, MO, USA.
Shi ChenHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Xianlin YangHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Jin YuanHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Xiaohong LiHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Li JiangHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Abbi SmithHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Waylan BesslerHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
George SanduskyDepartment of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA.
Anat Stemmer-RachamimovDepartment of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Timothy J StuhlmillerDepartment of Pharmacology, University of North Carolina, Chapel Hill, NC.
Steven P AngusDepartment of Pharmacology, University of North Carolina, Chapel Hill, NC.
Gary L JohnsonDepartment of Pharmacology, University of North Carolina, Chapel Hill, NC.
Grzegorz NalepaHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Charles W YatesDepartment of Otolaryngology, Indiana University School of Medicine, Indianapolis, IN, USA.
D Wade ClappHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Su-Jung ParkHerman B Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Indiana University School of MedicineIndiana University – Purdue University Indianapolis · USUniversity of North Carolina at Chapel Hill · USMassachusetts General Hospital · USWashington University in St. Louis · US

Funding

A Novel Approach to Treating Sensorineural Hearing loss and Inner Ear Disease in Neurofibromatosis Type 2 (NF2)F31DC016528 · NIDCD · INDIANA UNIVERSITY INDIANAPOLIS · PI HAWLEY, ERIC · 2018 to 2019
$35k
NIDCD NIH HHS F31 DC016528
6 · The paper itself

Abstract

Schwannomas are common, highly morbid and medically untreatable tumors that can arise in patients with germ line as well as somatic mutations in neurofibromatosis type 2 (NF2). These mutations most commonly result in the loss of function of the NF2-encoded protein, Merlin. Little is known about how Merlin functions endogenously as a tumor suppressor and how its loss leads to oncogenic transformation in Schwann cells (SCs). Here, we identify nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB)-inducing kinase (NIK) as a potential drug target driving NF-κB signaling and Merlin-deficient schwannoma genesis. Using a genomic approach to profile aberrant tumor signaling pathways, we describe multiple upregulated NF-κB signaling elements in human and murine schwannomas, leading us to identify a caspase-cleaved, proteasome-resistant NIK kinase domain fragment that amplifies pathogenic NF-κB signaling. Lentiviral-mediated transduction of this NIK fragment into normal SCs promotes proliferation, survival, and adhesion while inducing schwannoma formation in a novel in vivo orthotopic transplant model. Furthermore, we describe an NF-κB-potentiated hepatocyte growth factor (HGF) to MET proto-oncogene receptor tyrosine kinase (c-Met) autocrine feed-forward loop promoting SC proliferation. These innovative studies identify a novel signaling axis underlying schwannoma formation, revealing new and potentially druggable schwannoma vulnerabilities with future therapeutic potential.

Indexed as

AnimalsAutocrine CommunicationCarcinogenesisCaspase 1Cell ProliferationDisease Models, AnimalGene Expression Regulation, NeoplasticHepatocyte Growth FactorHumansMiceMolecular Targeted TherapyNeurilemmomaNeurofibromatosis 2Neurofibromin 2NF-kappa BNF-kappaB-Inducing KinaseCaspase 1Hepatocyte Growth FactorHGF protein, humanMAS1 protein, humanNeurofibromin 2NF-kappa BNF-kappaB-Inducing KinaseProteasome Endopeptidase ComplexProtein Serine-Threonine KinasesProto-Oncogene MasProto-Oncogene Proteins c-met

Identifiers

PMID30335132
PMCPMC6489415
OpenAlexW2896989198

What OpenQuestion holds

Textmetadata
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.