Evidence map›Paper›PMID 33483902›Full record

ArticleMolecular neurobiology2021

DNA Methyltransferase 1 Is Dysregulated in Parkinson's Disease via Mediation of miR-17.

Hong-Qiu Zhang, Jian-Yong Wang, Zhao-Feng Li, Lei Cui, Shi-Shi Huang, Lan-Bing Zhu, Yue Sun, Rui Yang, Hui-Hui Fan, Xiong Zhang and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  5. Epigenetic mechanisms of Parkinson's disease and potential epigenetic-based therapeutics.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  6. Review
  7. MicroRNAs and synaptic dysfunction in Parkinson's disease.Molecular therapy. Nucleic acids · 2025
    Review
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  10. Identifying the potential role of serum miR-20a as a biomarker for olfactory dysfunction in patients with Parkinson's disease.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2023
    Article
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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

11 authors at 1 institution in 2 countries.

Hong-Qiu Zhang *Department of Preventive Medicine, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China.
Jian-Yong Wang *Department of Geriatrics and Neurology, the Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China.
Zhao-Feng LiDepartment of Preventive Medicine, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China.
Lei CuiDepartment of Preventive Medicine, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China.
Shi-Shi HuangDepartment of Geriatrics and Neurology, the Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China.
Lan-Bing ZhuDepartment of Geriatrics and Neurology, the Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China.
Yue SunDepartment of Geriatrics and Neurology, the Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China.
Rui YangDepartment of Preventive Medicine, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China.
Hui-Hui FanDepartment of Preventive Medicine, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China.
Xiong ZhangDepartment of Geriatrics and Neurology, the Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, 325027, Zhejiang, China. zhangxiong98@gmail.com.
Jian-Hong ZhuDepartment of Preventive Medicine, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China. jhzhu@wmu.edu.cn.ORCID http://orcid.org/0000-0001-9412-8264
Wenzhou Medical University · CN

Funding

National Natural Science Foundation of China 31701080National Natural Science Foundation of China 81771380National Natural Science Foundation of China 81771510National Natural Science Foundation of China 81801271Natural Science Foundation of Zhejiang Province LD19H090001Natural Science Foundation of Zhejiang Province LZ19H090002Wenzhou Municipal Science and Technology Bureau C20170003Wenzhou Municipal Science and Technology Bureau Y20190074zhejiang of Science and Technology Department (CN) 2018C37111Zhejiang Provincial Medical Technology Program 2018KY120Zhejiang Provincial Medical Technology Program 2019KY445
6 · The paper itself

Abstract

Aberrant DNA methylation is closely associated with the pathogenesis of Parkinson's disease (PD). DNA methyltransferases (DNMTs) are the enzymes for establishment and maintenance of DNA methylation patterns. It has not been clearly defined how DNMTs respond in PD and what mechanisms are associated. Models of PD were established by treatment of five different neurotoxins in cells and intraperitoneal injection of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice. Plasma samples of PD patients were also used. Western blot, real-time PCR, immunostaining, and/or luciferase reporter were employed. DNA methylation was analyzed by the bisulfite sequencing analysis. Protein expression of DNMT1, but not of DNMT3A and DNMT3B, was reduced in the cellular and mouse models of PD. Paradoxically, mRNA levels of DNMT1 were increased in these models. After ruling out the possibility of protein degradation, we screened a set of miRNAs that potentially targeted DNMT1 3'-UTR by luciferase reporters and expression abundancies. miR-17 was identified for further investigation with miR-19a of low expression as a parallel comparison. Although exogenous transfection of either miR-17 or miR-19a mimics could inhibit DNMT1 expression, results of miRNA inhibitors showed that miR-17, but not miR-19a, endogenously regulated DNMT1 and the subsequent DNA methylation. Furthermore, levels of miR-17 were elevated in the neurotoxin-induced PD models and the plasma of PD patients. This study demonstrates that the miR-17-mediated DNMT1 downregulation underlies the aberrant DNA methylation in PD. Our results provide a link bridging environmental insults and epigenetic changes and implicate miR-17 in therapeutical modulation of DNA methylation in PD.

Indexed as

1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineAnimalsCell Line, TumorDisease Models, AnimalDNA (Cytosine-5-)-Methyltransferase 1DNA MethylationGene Expression RegulationHumansLysosomesMaleMiceMice, Inbred C57BLMicroRNAsModels, BiologicalNeurotoxinsParkinson Disease1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridineDNA (Cytosine-5-)-Methyltransferase 1MicroRNAsMIRN17 microRNA, humanMIRN19A microRNA, humanNeurotoxinsRNA, MessengerDNA methylationDNMT1miR-17miRNAParkinson’s disease

Identifiers

PMID33483902
OpenAlexW3124388849

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.