Evidence map›Paper›PMID 29670079›Full record

ArticleCell death & disease2018

Upregulation of neuronal astrocyte elevated gene-1 protects nigral dopaminergic neurons in vivo.

Eunju Leem, Hyung-Jun Kim, Minji Choi, Sehwan Kim, Yong-Seok Oh, Kea Joo Lee, Young-Shik Choe, Jae-Young Um, Won-Ho Shin, Jae Yeong Jeong and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Expression patterns of AEG-1 in the normal brain.Brain structure & function · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. 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

20 authors at 11 institutions in 3 countries.

Eunju LeemSchool of Life Sciences, BK21 Plus KNU Creative BioResearch Group, Institute of Life Science & Biotechnology, Kyungpook National University, Daegu, 41566, Republic of Korea.
Hyung-Jun KimDepartment of Neural Development and Disease, Department of Structure & Function of Neural Network, Korea Brain Research Institute, Daegu, 41062, Republic of Korea.
Minji ChoiDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Sehwan KimSchool of Life Sciences, BK21 Plus KNU Creative BioResearch Group, Institute of Life Science & Biotechnology, Kyungpook National University, Daegu, 41566, Republic of Korea.
Yong-Seok OhDepartment of Brain-Cognitive Science, Daegu-Gyeongbuk Institute of Science and Technology, Daegu, 42988, Republic of Korea.ORCID 0000-0002-9039-2014
Kea Joo LeeDepartment of Neural Development and Disease, Department of Structure & Function of Neural Network, Korea Brain Research Institute, Daegu, 41062, Republic of Korea.
Young-Shik ChoeDepartment of Neural Development and Disease, Department of Structure & Function of Neural Network, Korea Brain Research Institute, Daegu, 41062, Republic of Korea.
Jae-Young UmDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.ORCID 0000-0002-0568-9738
Won-Ho ShinPredictive Model Research Center, Korea Institute of Toxicology, Korea Research Institute of Chemical Technology, Daejeon, 34114, Republic of Korea.
Jae Yeong JeongPredictive Model Research Center, Korea Institute of Toxicology, Korea Research Institute of Chemical Technology, Daejeon, 34114, Republic of Korea.
Byung Kwan JinDepartment of Biochemisry and Molecular Biology, Department of Neuroscience Graduate School, School of Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.
Dong Woon KimDepartment of Anatomy, Brain Research Institute, School of Medicine, Chungnam National University, Daejeon, 34134, Republic of Korea.ORCID 0000-0001-7691-1394
Catriona McLeanVictorian Brain Bank Network, Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Melbourne, VIC, 3004, Australia.
Paul B FisherDepartment of Human and Molecular Genetics, VCU Institute of Molecular Medicine, VCU Massey Cancer Center, School of Medicine, Virginia Commonwealth University, Richmond, VA, 23298, USA.
Nikolai KholodilovDepartment of Neurology, Columbia University, New York, NY, 10032, USA.
Kwang Seok AhnDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.
Jae Man LeeDepartment of Biochemistry and Cell Biology, Cell and Matrix Research Institute, BK21 Plus KNU Biomedical Convergence Program, School of Medicine, Kyungpook National University, Daegu, 41944, Republic of Korea.
Un Ju JungDepartment of Food Science and Nutrition, Pukyong National University, Busan, 48513, Republic of Korea.
Seok-Geun LeeDepartment of Science in Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea. seokgeun@khu.ac.kr.ORCID 0000-0002-0060-5777
Sang Ryong KimSchool of Life Sciences, BK21 Plus KNU Creative BioResearch Group, Institute of Life Science & Biotechnology, Kyungpook National University, Daegu, 41566, Republic of Korea. srk75@knu.ac.kr.ORCID 0000-0003-0299-1613
Kyung Hee University · KRKyungpook National University · KRKorea Brain Research Institute · KRChungnam National University · KRColumbia University · USDaegu Gyeongbuk Institute of Science and Technology · KRKorea Institute of Toxicology · KRKyung Hee Cyber University · KRPukyong National University · KRThe University of Melbourne · AUVirginia Commonwealth University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of astrocyte elevated gene-1 (AEG-1) in nigral dopaminergic (DA) neurons has not been studied. Here we report that the expression of AEG-1 was significantly lower in DA neurons in the postmortem substantia nigra of patients with Parkinson's disease (PD) compared to age-matched controls. Similarly, decreased AEG-1 levels were found in the 6-hydroxydopamine (6-OHDA) mouse model of PD. An adeno-associated virus-induced increase in the expression of AEG-1 attenuated the 6-OHDA-triggered apoptotic death of nigral DA neurons. Moreover, the neuroprotection conferred by the AEG-1 upregulation significantly intensified the neurorestorative effects of the constitutively active ras homolog enriched in the brain [Rheb(S16H)]. Collectively, these results demonstrated that the sustained level of AEG-1 as an important anti-apoptotic factor in nigral DA neurons might potentiate the therapeutic effects of treatments, such as Rheb(S16H) administration, on the degeneration of the DA pathway that characterizes PD.

Indexed as

ApoptosisUp-RegulationAnimalsAstrocytesDisease Models, AnimalDopaminergic NeuronsHumansMembrane GlycoproteinsMiceOxidopamineParkinson Disease, SecondaryRas Homolog Enriched in Brain ProteinSubstantia NigraCrisp1 protein, mouseMembrane GlycoproteinsOxidopamineRas Homolog Enriched in Brain ProteinRheb protein, mouse

Identifiers

PMID29670079
PMCPMC5906475
OpenAlexW2802358340

What OpenQuestion holds

Textmetadata
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.