Evidence map›Paper›PMID 24352657›Full record

ArticleThe Journal of biological chemistry2014

scyllo-Inositol promotes robust mutant Huntingtin protein degradation.

Aaron Y Lai, Cynthia P Lan, Salwa Hasan, Mary E Brown, Joanne McLaurin

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Aaron Y LaiFrom the Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario M5S 1A8, Canada.
Cynthia P Lan
Salwa Hasan
Mary E Brown
Joanne McLaurin
University of Toronto · CA

Funding

Canadian Institutes of Health Research 120894Canadian Institutes of Health Research PRG37857
6 · The paper itself

Abstract

Huntington disease is characterized by neuronal aggregates and inclusions containing polyglutamine-expanded huntingtin protein and peptide fragments (polyQ-Htt). We have used an established cell-based assay employing a PC12 cell line overexpressing truncated exon 1 of Htt with a 103-residue polyQ expansion that yields polyQ-Htt aggregates to investigate the fate of polyQ-Htt-drug complexes. scyllo-Inositol is an endogenous inositol stereoisomer known to inhibit accumulation and toxicity of the amyloid-β peptide and α-synuclein. In light of these properties, we investigated the effect of scyllo-inositol on polyQ-Htt accumulation. We show that scyllo-inositol lowered the number of visible polyQ-Htt aggregates and robustly decreased polyQ-Htt protein abundance without concomitant cellular toxicity. We found that scyllo-inositol-induced polyQ-Htt reduction was by rescue of degradation pathways mediated by the lysosome and by the proteasome but not autophagosomes. The rescue of degradation pathways was not a direct result of scyllo-inositol on the lysosome or proteasome but due to scyllo-inositol-induced reduction in mutant polyQ-Htt protein levels.

Indexed as

Mutationalpha-SynucleinAmyloid beta-PeptidesAnimalsHuntingtin ProteinInositolLysosomesNerve Tissue ProteinsNuclear ProteinsPC12 CellsPeptidesProteasome Endopeptidase ComplexProteolysisRatsalpha-SynucleinAmyloid beta-PeptidesHtt protein, ratHuntingtin ProteinInositolNerve Tissue ProteinsNuclear ProteinsPeptidespolyglutamineProteasome Endopeptidase ComplexscyllitolSnca protein, ratAutophagyhuntingtinHuntington DiseaseLysosomesNeurodegenerative DiseasesProteasomescyllo-Inositol

Identifiers

PMID24352657
PMCPMC3916565
OpenAlexW1988667567

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.