Evidence map›Paper›PMID 30974833›Full record

ArticleInternational journal of molecular sciences2019

Rhododendrin-Induced RNF146 Expression via Estrogen Receptor β Activation is Cytoprotective Against 6-OHDA-Induced Oxidative Stress.

Hyojung Kim, Jisoo Park, HyunHee Leem, MyoungLae Cho, Jin-Ha Yoon, Han-Joo Maeng, Yunjong Lee

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. 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
0.8field-weighted citation impact, top 25% 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, 13 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

7 authors at 3 institutions in 1 country.

Hyojung KimDivision of Pharmacology, Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Samsung Biomedical Research Institute, Suwon, Gyeonggi-do 440-746, Korea. hjung93@skku.edu.
Jisoo ParkDivision of Pharmacology, Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Samsung Biomedical Research Institute, Suwon, Gyeonggi-do 440-746, Korea. zysu0728@skku.edu.
HyunHee LeemNational Development Institute of Korean Medicine, Gyeongsan 38540, Korea. npb0391@nikom.or.kr.
MyoungLae ChoNational Development Institute of Korean Medicine, Gyeongsan 38540, Korea. meanglae@nikom.or.kr.
Jin-Ha YoonCollege of Pharmacy, Gachon University, Incheon 21936, Korea. jinha89@daum.net.
Han-Joo MaengCollege of Pharmacy, Gachon University, Incheon 21936, Korea. hjmaeng@gachon.ac.kr.
Yunjong LeeDivision of Pharmacology, Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Samsung Biomedical Research Institute, Suwon, Gyeonggi-do 440-746, Korea. ylee69@skku.edu.ORCID 0000-0003-0182-2279
Samsung (South Korea) · KRGachon University · KRNational Development Institute of Korean Medicine · KR

Funding

National Research Foundation of Korea 2017M3C7A1043848
6 · The paper itself

Abstract

Ring finger protein 146 (RNF146) is an E3 ubiquitin ligase whose activity prevents poly (ADP-ribose) polymerase 1 (PARP1)-dependent neurodegeneration in Parkinson's disease (PD). Previously, we reported that rhododendrin is a chemical inducer that increases RNF146 expression. However, the molecular mechanism of rhododendrin-induced RNF146 expression is largely unknown and its translational application for the treatment of Parkinson's disease remains unexplored. Here we found that rhododendrin increased RNF146 expression via estrogen receptor β (ERβ) activation. Rhododendrin stimulated ERβ nuclear translocation and binding to the RNF146 promoter, thereby enhancing its transcription. Rhododendrin is cytoprotective against 6-hydroxydopamine (6-OHDA)-induced cell death, which is largely dependent on ERβ activity and RNF146 expression. Finally, we demonstrated that rhododendrin treatment resulted in RNF146 expression in dopaminergic neurons in mice. Moreover, dopaminergic neuron viability was markedly enhanced by pretreatment with rhododendrin in 6-OHDA-induced mouse models for PD. Our findings indicate that estrogen receptor activation plays a neuroprotective role and that rhododendrin could be a potential therapeutic agent in preventing PARP1-dependent dopaminergic cell loss in PD.

Indexed as

AnimalsCell Line, TumorDopaminergic NeuronsEstrogen Receptor betaGene Expression Regulation, EnzymologicGlycosidesHumansMaleMiceOxidative StressOxidopamineParkinson DiseasePhenolsUbiquitin-Protein LigasesESR2 protein, humanEstrogen Receptor betaGlycosidesOxidopaminePhenolsrhododendrinRNF146 protein, humanRnf146 protein, mouseUbiquitin-Protein Ligasesdopaminergic neurodegenerationestrogen receptorParkinson’s diseasepoly (ADP-ribose)rhododendrinRNF146

Identifiers

PMID30974833
PMCPMC6479468
OpenAlexW2939746862

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.