Evidence map›Paper›PMID 28359145›Full record

ArticleMolecules and cells2017

Neuroprotective Effects of Protein Tyrosine Phosphatase 1B Inhibition against ER Stress-Induced Toxicity.

Yu-Mi Jeon, Shinrye Lee, Seyeon Kim, Younghwi Kwon, Kiyoung Kim, Chang Geon Chung, Seongsoo Lee, Sung Bae Lee, Hyung-Jun Kim

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 31 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

9 authors at 4 institutions in 1 country.

Yu-Mi JeonDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu 41068, Korea.
Shinrye LeeDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu 41068, Korea.
Seyeon KimDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu 41068, Korea.
Younghwi KwonDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu 41068, Korea.
Kiyoung KimDepartment of Medical Biotechnology, Soonchunhyang University, Asan 31538, Korea.
Chang Geon ChungDepartment of Brain & Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea.
Seongsoo LeeGwangju Center, Korea Basic Science Institute (KBSI), Gwangju 61186, Korea.
Sung Bae LeeDepartment of Brain & Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 42988, Korea.
Hyung-Jun KimDepartment of Neural Development and Disease, Korea Brain Research Institute (KBRI), Daegu 41068, Korea.
Korea Brain Research Institute · KRDaegu Gyeongbuk Institute of Science and Technology · KRKorea Basic Science Institute · KRSoonchunhyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several lines of evidence suggest that endoplasmic reticulum (ER) stress plays a critical role in the pathogenesis of many neurodegenerative diseases such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis. Protein tyrosine phosphatase 1B (PTP1B) is known to regulate the ER stress signaling pathway, but its role in neuronal systems in terms of ER stress remains largely unknown. Here, we showed that rotenone-induced toxicity in human neuroblastoma cell lines and mouse primary cortical neurons was ameliorated by PTP1B inhibition. Moreover, the increase in the level of ER stress markers (eIF2α phosphorylation and PERK phosphorylation) induced by rotenone treatment was obviously suppressed by concomitant PTP1B inhibition. However, the rotenone-induced production of reactive oxygen species (ROS) was not affected by PTP1B inhibition, suggesting that the neuroprotective effect of the PTP1B inhibitor is not associated with ROS production. Moreover, we found that MG132-induced toxicity involving proteasome inhibition was also ameliorated by PTP1B inhibition in a human neuroblastoma cell line and mouse primary cortical neurons. Consistently, downregulation of the PTP1B homologue gene in

Indexed as

NeuroprotectionAnimalsCell DeathCerebral CortexDown-RegulationDrosophilaeIF-2 KinaseEndoplasmic Reticulum StressEukaryotic Initiation Factor-2HumansLeupeptinsMiceNeurodegenerative DiseasesNeuronsPhosphorylationProtein Tyrosine Phosphatase, Non-Receptor Type 1benzyloxycarbonylleucyl-leucyl-leucine aldehydeeIF-2 KinaseEukaryotic Initiation Factor-2LeupeptinsProtein Tyrosine Phosphatase, Non-Receptor Type 1Reactive Oxygen SpeciesRotenoneUncoupling Agentsendoplasmic reticulum stress (ER Stress)MG132reactive oxygen species (ROS)rotenoneubiquitin proteasome system

Identifiers

PMID28359145
PMCPMC5424274
OpenAlexW2616536928

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.