Evidence map›Paper›PMID 30266739›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2018

MBD1 Contributes to the Genesis of Acute Pain and Neuropathic Pain by Epigenetic Silencing of

Kai Mo, Shaogen Wu, Xiyao Gu, Ming Xiong, Weihua Cai, Fidelis E Atianjoh, Emily E Jobe, Xinyu Zhao, Wei-Feng Tu, Yuan-Xiang Tao

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 56 citations in OpenAlex.

  1. MBD1-Mediated SDHD Methylation Aggravates Preeclampsia Progression via Triggering Mitochondrial Dysfunction.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
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  6. Review
  7. Article
  8. Review
  9. Epigenetic Landscapes of Pain: DNA Methylation Dynamics in Chronic Pain.International journal of molecular sciences · 2024
    Review
  10. Article
  11. Review
  12. Transcription factor EBF1 mitigates neuropathic pain by rescuing Kv1.2 expression in primary sensory neurons.Translational research : the journal of laboratory and clinical medicine · 2024
    Article
  13. The Epigenetics of Neuropathic Pain: A Systematic Update.International journal of molecular sciences · 2023
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. The Downregulation of Opioid Receptors and Neuropathic Pain.International journal of molecular sciences · 2023
    Review
  20. Epigenetic Modulation of Opioid Receptors by Drugs of Abuse.International journal of molecular sciences · 2022
    Review
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

10 authors at 3 institutions in 2 countries.

Kai MoDepartment of Anesthesiology, New Jersey Medical School, Rutgers State University of New Jersey, Newark, New Jersey 07013.ORCID 0000-0003-1738-746X
Shaogen WuDepartment of Anesthesiology, New Jersey Medical School, Rutgers State University of New Jersey, Newark, New Jersey 07013.ORCID 0000-0001-5653-3357
Xiyao GuDepartment of Anesthesiology, New Jersey Medical School, Rutgers State University of New Jersey, Newark, New Jersey 07013.
Ming XiongDepartment of Anesthesiology, New Jersey Medical School, Rutgers State University of New Jersey, Newark, New Jersey 07013.
Weihua CaiDepartment of Anesthesiology, New Jersey Medical School, Rutgers State University of New Jersey, Newark, New Jersey 07013.
Fidelis E AtianjohDepartment of Anesthesiology, New Jersey Medical School, Rutgers State University of New Jersey, Newark, New Jersey 07013.
Emily E JobeDepartment of Neuroscience, University of Wisconsin-Madison, Madison, Wisconsin 53705.
Xinyu ZhaoDepartment of Neuroscience, University of Wisconsin-Madison, Madison, Wisconsin 53705.
Wei-Feng TuDepartment of Anesthesiology, Guangzhou General Hospital of Guangzhou Military Region, Southern Medical University, Guangzhou 510010, China, yuanxiang.tao@njms.rutgers.edu wftuyx02@163.com.
Yuan-Xiang TaoDepartment of Anesthesiology, New Jersey Medical School, Rutgers State University of New Jersey, Newark, New Jersey 07013, yuanxiang.tao@njms.rutgers.edu wftuyx02@163.com.ORCID 0000-0003-1777-3272
Rutgers, The State University of New Jersey · USUniversity of Wisconsin–Madison · USGeneral Hospital of Guangzhou Military Command · CN

Funding

Role of small RNAs in NeurogenesisR01MH080434 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI ZHAO, XINYU · 2007 to 2015
$2.9M
Dissection of a new spinal cord circuit in pain sensationR01NS094224 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI LUO, WENQIN · 2016 to 2020
$2.5M
Epigenetic regulation of neuropathic pain: Role of DRG histone methyltransferase G9aR01NS094664 · NINDS · RBHS-NEW JERSEY MEDICAL SCHOOL · PI TAO, YUAN-XIANG · 2016 to 2020
$2.0M
mTOR, a new target for opioid-induced tolerance and hyperalgesiaR01DA033390 · NIDA · RBHS-NEW JERSEY MEDICAL SCHOOL · PI TAO, YUAN-XIANG · 2013 to 2017
$1.8M
Coordinate actions between methyl-CpG binding proteins in neuronal developmentR21NS095632 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI ZHAO, XINYU · 2015 to 2016
$418k
Epigenetic Crosstalk Regulates Neuronal DevelopmentR56MH113146 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI ZHAO, XINYU · 2017 to 2017
$383k
NIDA NIH HHS R01 DA033390NIMH NIH HHS R01 MH080434NIMH NIH HHS R56 MH113146NINDS NIH HHS R01 NS094224NINDS NIH HHS R01 NS094664NINDS NIH HHS R21 NS095632
6 · The paper itself

Abstract

The transmission of normal sensory and/or acute noxious information requires intact expression of pain-associated genes within the pain pathways of nervous system. Expressional changes of these genes after peripheral nerve injury are also critical for neuropathic pain induction and maintenance. Methyl-CpG-binding domain protein 1 (MBD1), an epigenetic repressor, regulates gene transcriptional activity. We report here that MBD1 in the primary sensory neurons of DRG is critical for the genesis of acute pain and neuropathic pain as DRG MBD1-deficient mice exhibit the reduced responses to acute mechanical, heat, cold, and capsaicin stimuli and the blunted nerve injury-induced pain hypersensitivities. Furthermore, DRG overexpression of MBD1 leads to spontaneous pain and evoked pain hypersensitivities in the WT mice and restores acute pain sensitivities in the MBD1-deficient mice. Mechanistically, MDB1 represses

Indexed as

Acute PainAnimalsCells, CulturedDNA-Binding ProteinsEpigenesis, GeneticGanglia, SpinalGene SilencingKv1.2 Potassium ChannelMaleMiceMice, Inbred C57BLMice, KnockoutNeuralgiaReceptors, Opioid, muSensory Receptor CellsDNA-Binding ProteinsKcna2 protein, mouseKv1.2 Potassium ChannelMbd1 protein, mouseOprm protein, mouseReceptors, Opioid, muacute painDRGKv1.2MBD1mu opioid receptorneuropathic pain

Identifiers

PMID30266739
PMCPMC6234297
OpenAlexW2893032714

What OpenQuestion holds

Textmetadata
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.