Evidence map›Paper›PMID 26679228›Full record

ReviewNeuroscience letters2016

Selective repression of gene expression in neuropathic pain by the neuron-restrictive silencing factor/repressor element-1 silencing transcription (NRSF/REST).

Dianna E Willis, Meng Wang, Elizabeth Brown, Lilah Fones, John W Cave

Abstract readReview
In one paragraph

Review in Neuroscience letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. The Epigenetics of Neuropathic Pain: A Systematic Update.International journal of molecular sciences · 2023
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. KFrontiers in cellular neuroscience · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. M-type KBritish journal of pharmacology · 2018
    Review
  16. Article
  17. 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

5 authors at 3 institutions in 1 country.

Dianna E WillisBurke Medical Research Institute, 785 Mamaroneck Ave., White Plains, NY 10605, United States; Brain and Mind Research Institute, Weill Cornell Medical College, 1300 York Ave, NY, NY 10065, United States.
Meng WangBurke Medical Research Institute, 785 Mamaroneck Ave., White Plains, NY 10605, United States.
Elizabeth BrownBurke Medical Research Institute, 785 Mamaroneck Ave., White Plains, NY 10605, United States.
Lilah FonesBurke Medical Research Institute, 785 Mamaroneck Ave., White Plains, NY 10605, United States.
John W CaveBurke Medical Research Institute, 785 Mamaroneck Ave., White Plains, NY 10605, United States; Brain and Mind Research Institute, Weill Cornell Medical College, 1300 York Ave, NY, NY 10065, United States. Electronic address: joc2042@med.cornell.edu.
Burke Medical Research Institute · USCornell University · USMIND Research Institute · US

Funding

Plasticity in the Aging Olfactory SystemR01DC008955 · NIDCD · WINIFRED MASTERSON BURKE MED RES INST · PI BAKER, HARRIET D., CAVE, JOHN W · 2008 to 2015
$4.6M
Axonal Transport and Local Translation in Neuropathic PainR00NR010797 · NINR · WINIFRED MASTERSON BURKE MED RES INST · PI WILLIS, DIANNA E. · 2010 to 2012
$733k
Axonal Transport and Local Translation in Neuropathic PainK99NR010797 · NINR · NEMOURS CHILDREN'S HOSPITAL, DELAWARE · PI WILLIS, DIANNA E. · 2007 to 2008
$174k
NIDCD NIH HHS R01 DC008955NINR NIH HHS K99 NR010797NINR NIH HHS R00 NR010797
6 · The paper itself

Abstract

Neuropathic pain often develops following nerve injury as a result of maladaptive changes that occur in the injured nerve and along the nociceptive pathways of the peripheral and central nervous systems. Multiple cellular and molecular mechanisms likely account for these changes; however, the exact nature of these mechanisms remain largely unknown. A growing number of studies suggest that alteration in gene expression is an important step in the progression from acute to chronic pain states and epigenetic regulation has been proposed to drive this change in gene expression. In this review, we discuss recent evidence that the DNA-binding protein neuron-restrictive silencing factor/repressor element-1 silencing transcription factor (NRSF/REST) is an important component in the development and maintenance of neuropathic pain through its role as a transcriptional regulator for a select subset of genes that it normally represses during development.

Indexed as

Epigenesis, GeneticGene Expression RegulationAnimalsHumansNeuralgiaRE1-Silencing Transcription FactorRepressor ProteinsRE1-Silencing Transcription FactorRepressor ProteinsEpigeneticsMeCP2Neuropathic painNRSF/REST

Identifiers

PMID26679228
PMCPMC4899316
OpenAlexW2196208118

What OpenQuestion holds

Textmetadata
LicenceTDM
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.