Evidence map›Paper›PMID 32199908›Full record

ArticleNeurobiology of disease2020

Inactivation of Hippo and cJun-N-terminal Kinase (JNK) signaling mitigate FUS mediated neurodegeneration in vivo.

Neha Gogia, Ankita Sarkar, Abijeet Singh Mehta, Nandini Ramesh, Prajakta Deshpande, Madhuri Kango-Singh, Udai Bhan Pandey, Amit Singh

Open access · goldAbstract read
In one paragraph

Article in Neurobiology of disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Toxic mechanisms of amyloid oligomers and therapeutic strategies.Protein science : a publication of the Protein Society · 2026
    Review
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  6. Article
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  8. Article
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  11. Article
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  15. Review
  16. Journal of developmental biology · 2022
    Review
  17. Pathophysiology of stress granules: An emerging link to diseases (Review).International journal of molecular medicine · 2022
    Review
  18. Article
  19. Endothelin-1, over-expressed in SOD1Frontiers in cellular neuroscience · 2022
    Article
  20. Article
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

8 authors at 2 institutions in 1 country.

Neha GogiaDepartment of Biology, University of Dayton, Dayton, OH 45469, USA.
Ankita SarkarDepartment of Biology, University of Dayton, Dayton, OH 45469, USA.
Abijeet Singh MehtaDepartment of Biology, University of Dayton, Dayton, OH 45469, USA.
Nandini RameshDepartment of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, PA, USA.
Prajakta DeshpandeDepartment of Biology, University of Dayton, Dayton, OH 45469, USA.
Madhuri Kango-SinghDepartment of Biology, University of Dayton, Dayton, OH 45469, USA; Premedical Program, University of Dayton, Dayton, OH 45469, USA; Center for Tissue Regeneration and Engineering at Dayton (TREND), University of Dayton, Dayton, OH 45469, USA.
Udai Bhan PandeyDepartment of Pediatrics, Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, PA, USA.
Amit SinghDepartment of Biology, University of Dayton, Dayton, OH 45469, USA; Premedical Program, University of Dayton, Dayton, OH 45469, USA; Center for Tissue Regeneration and Engineering at Dayton (TREND), University of Dayton, Dayton, OH 45469, USA; The Integrative Science and Engineering Center, University of Dayton, Dayton, OH 45469, USA; Center for Genomic Advocacy (TCGA), Indiana State University, Terre Haute, IN, USA. Electronic address: asingh1@udayton.edu.
University of Dayton · USUniversity of Pittsburgh · US

Funding

Novel role of compensatory proliferation in human brain tumorR01CA183991 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NAKANO, ICHIRO · 2015 to 2019
$1.6M
Genetic Basis of Patterning and Growth in Drosophila EyeR15GM124654 · NIGMS · UNIVERSITY OF DAYTON · PI SINGH, AMIT · 2017 to 2017
$439k
Drosophila models for ubiquilin-associated ALSR21NS101661 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI PANDEY, UDAI B, TIBBETTS, RANDAL SCOT · 2017 to 2018
$422k
Oligonucleotide approach to antagonize neurotoxic TDP-43 assemblies in dementiaR21AG064940 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DONNELLY, CHRISTOPHER JAMES, PANDEY, UDAI B · 2019 to 2020
$417k
Targeting epigenetic modifiers of androgen receptor activity and toxicity in SBMAR21NS111768 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PANDEY, UDAI B · 2019 to 2019
$397k
Genetic Control of Axial Patterning in Drosophila EyeR15HD064557 · NICHD · UNIVERSITY OF DAYTON · PI SINGH, AMIT · 2010 to 2010
$218k
NCI NIH HHS R01 CA183991NIA NIH HHS R21 AG064940NICHD NIH HHS R15 HD064557NIGMS NIH HHS R15 GM124654NINDS NIH HHS R21 NS101661NINDS NIH HHS R21 NS111768
6 · The paper itself

Abstract

Amyotrophic Lateral Sclerosis (ALS), a late-onset neurodegenerative disorder characterized by the loss of motor neurons in the central nervous system, has no known cure to-date. Disease causing mutations in human Fused in Sarcoma (FUS) leads to aggressive and juvenile onset of ALS. FUS is a well-conserved protein across different species, which plays a crucial role in regulating different aspects of RNA metabolism. Targeted misexpression of FUS in Drosophila model recapitulates several interesting phenotypes relevant to ALS including cytoplasmic mislocalization, defects at the neuromuscular junction and motor dysfunction. We screened for the genetic modifiers of human FUS-mediated neurodegenerative phenotype using molecularly defined deficiencies. We identified hippo (hpo), a component of the evolutionarily conserved Hippo growth regulatory pathway, as a genetic modifier of FUS mediated neurodegeneration. Gain-of-function of hpo triggers cell death whereas its loss-of-function promotes cell proliferation. Downregulation of the Hippo signaling pathway, using mutants of Hippo signaling, exhibit rescue of FUS-mediated neurodegeneration in the Drosophila eye, as evident from reduction in the number of TUNEL positive nuclei as well as rescue of axonal targeting from the retina to the brain. The Hippo pathway activates c-Jun amino-terminal (NH

Indexed as

Amyotrophic Lateral SclerosisAnimalsAxonsCytoplasmDisease Models, AnimalDrosophilaDrosophila ProteinsHippo KinasesIntracellular Signaling Peptides and ProteinsMAP Kinase Kinase 4Motor NeuronsMutationNerve DegenerationNeuromuscular JunctionPhenotypeProtein Serine-Threonine KinasesDrosophila ProteinsHippo Kinaseshpo protein, DrosophilaIntracellular Signaling Peptides and ProteinsMAP Kinase Kinase 4Protein Serine-Threonine KinasesRNA-Binding Protein FUSAmyotrophic Lateral Sclerosis (ALS)Cell deathDrosophila eyeFused in Sarcoma (FUS)Hippo pathwayJNK signalingNeurodegenerationTranslocated in Liposarcoma (TLS)

Identifiers

PMID32199908
PMCPMC9277911
OpenAlexW3011711280

What OpenQuestion 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 OpenQuestion graph.