Evidence map›Paper›PMID 27074563›Full record

ArticleOncotarget2016

Hinokitiol protects primary neuron cells against prion peptide-induced toxicity via autophagy flux regulated by hypoxia inducing factor-1.

Ji-Hong Moon, Ju-Hee Lee, You-Jin Lee, Sang-Youel Park

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Isolation of Anti-Prion Compounds fromMolecules (Basel, Switzerland) · 2024
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. An Update on Autophagy in Prion Diseases.Frontiers in bioengineering and biotechnology · 2020
    Review
  9. Article
  10. Autophagy pathways in the treatment of prion diseases.Current opinion in pharmacology · 2019
    Review
  11. Recent Advances in Studies of Molecular Hydrogen against Sepsis.International journal of biological sciences · 2019
    Review
  12. Article
  13. Hydrogen-Rich Saline Activated Autophagy via HIF-1BioMed research international · 2018
    Article
  14. Review
  15. Article
  16. 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

4 authors at 1 institution in 1 country.

Ji-Hong MoonBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jeonbuk, South Korea.
Ju-Hee LeeBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jeonbuk, South Korea.
You-Jin LeeBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jeonbuk, South Korea.
Sang-Youel ParkBiosafety Research Institute, College of Veterinary Medicine, Chonbuk National University, Iksan, Jeonbuk, South Korea.
Jeonbuk National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prion diseases are fatal neurodegenerative disorders that are derived from structural changes of the native PrPc. Recent studies indicated that hinokitiol induced autophagy known to major function that keeps cells alive under stressful conditions. We investigated whether hinokitiol induces autophagy and attenuates PrP (106-126)-induced neurotoxicity. We observed increase of LC3-II protein level, GFP-LC3 puncta by hinokitiol in neuronal cells. Addition to, electron microscopy showed that hinokitiol enhanced autophagic vacuoles in neuronal cells. We demonstrated that hinokitiol protects against PrP (106-126)-induced neurotoxicity via autophagy by using autophagy inhibitor, wortmannin and 3MA, and ATG5 small interfering RNA (siRNA). We checked hinokitiol activated the hypoxia-inducible factor-1α (HIF-1α) and identified that hinokitiol-induced HIF-1α regulated autophagy. Taken together, this study is the first report demonstrating that hinokitiol protected against prion protein-induced neurotoxicity via autophagy regulated by HIF-1α. We suggest that hinokitiol is a possible therapeutic strategy in neuronal disorders including prion disease.

Indexed as

AdenineAndrostadienesAnimalsApoptosisAutophagyAutophagy-Related Protein 5Cells, CulturedHumansHypoxia-Inducible Factor 1, alpha SubunitImmunohistochemistryIn Situ Nick-End LabelingMiceMicroscopy, Electron, TransmissionMonoterpenesNeuronsNeuroprotective Agents3-methyladenineAdenineAndrostadienesAtg5 protein, mouseAutophagy-Related Protein 5beta-thujaplicinHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitMonoterpenesNeuroprotective AgentsPeptide Fragmentsprion protein (106-126)PrionsProtein Kinase InhibitorsRNA, Small InterferingTropoloneWortmanninautophagyGerotargetHIF-1hinokitiolneurodegenerationprion protein

Identifiers

PMID27074563
PMCPMC5058655
OpenAlexW2321277505

What OpenQuestion holds

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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 OpenQuestion graph.