Evidence map›Paper›PMID 30391475›Full record

ReviewTranslational research : the journal of laboratory and clinical medicine2019

Epigenetics in amyotrophic lateral sclerosis: a role for histone post-translational modifications in neurodegenerative disease.

Seth A Bennett, Royena Tanaz, Samantha N Cobos, Mariana P Torrente

Open access · greenAbstract readReview
In one paragraph

Review in Translational research : the journal of laboratory and clinical medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

80 citing papers in PubMed, 126 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. ACS omega · 2025
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

20 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Seth A BennettDepartment of Chemistry, Brooklyn College, Brooklyn, NewYork; Ph.D. Program in Biochemistry, The Graduate Center of the City University of New York, New York, New York.
Royena TanazDepartment of Chemistry, Brooklyn College, Brooklyn, NewYork.
Samantha N CobosDepartment of Chemistry, Brooklyn College, Brooklyn, NewYork; Ph.D. Program in Chemistry, The Graduate Center of the City University of New York, New York, NY 10016.
Mariana P TorrenteDepartment of Chemistry, Brooklyn College, Brooklyn, NewYork; Ph.D. Programs in Chemistry, Biochemistry, and Biology, The Graduate Center of the City University of New York, New York, New York. Electronic address: mariana.torrente@brooklyn.cuny.edu.
The Graduate Center, CUNY · USBrooklyn College · US

Funding

Epigenetics In Neurodegenerative Disease: Targeting Histone Modifications in ALSK22NS091314 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI TORRENTE, MARIANA PLAZAS · 2015 to 2017
$536k
NINDS NIH HHS K22 NS091314
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is the third most common adult onset neurodegenerative disorder worldwide. It is generally characterized by progressive paralysis starting at the limbs ultimately leading to death caused by respiratory failure. There is no cure and current treatments fail to slow the progression of the disease. As such, new treatment options are desperately needed. Epigenetic targets are an attractive possibility because they are reversible. Epigenetics refers to heritable changes in gene expression unrelated to changes in DNA sequence. Three main epigenetic mechanisms include the methylation of DNA, microRNAs and the post-translational modification of histone proteins. Histone modifications occur in many amino acid residues and include phosphorylation, acetylation, methylation as well as other chemical moieties. Recent evidence points to a possible role for epigenetic mechanisms in the etiology of ALS. Here, we review recent advances linking ALS and epigenetics, with a strong focus on histone modifications. Both local and global changes in histone modification profiles are associated with ALS drawing attention to potential targets for future diagnostic and treatment approaches.

Indexed as

Epigenesis, GeneticProtein Processing, Post-TranslationalAcetylationAmyotrophic Lateral SclerosisAnimalsChromatin Assembly and DisassemblyDNA MethylationHistonesHumansMicroRNAsHistonesMicroRNAs3′-untranslated region3′-UTRALSAMPAamyotrophic lateral sclerosisC9orf72chromosome 9 open reading frame 72dipeptide repeat expansionDREfrontotemporal dementiaFTDFUSfused In sarcomaHATHCPHDAChigh-CpG-density promoterhistone acetyltransferasehistone deacetylaselow-molecular weight neurofilamentmicroRNAmiRNANFLpost-translational modificationPRMTprotein arginine N-methyltransferasePTMRISCRNA-induced silencing complexSIRTsirtuinSMNSOD1superoxide dismutase 1suppressor of variegation 3-9 homologue 1survival of motor neuronSUV39HTAR DNA-binding protein 43TDP-43α-amino-3-hydroxy-5-methyl-4-isoxazole propionic Acid

Identifiers

PMID30391475
PMCPMC6331271
OpenAlexW2896272078

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.