Evidence map›Paper›PMID 24037427›Full record

ReviewNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2013

Sirtuin deacetylases as therapeutic targets in the nervous system.

Brett Langley, Anthony Sauve

Open access · hybridAbstract readReview
In one paragraph

Review in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Role of NADCellular and molecular neurobiology · 2023
    Review
  10. Transcriptional regulation ofMolecular medicine reports · 2022
    Article
  11. SIRT2 Inhibition Improves Functional Motor Recovery After Peripheral Nerve Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2020
    Article
  12. Article
  13. Article
  14. Dihydronicotinamide riboside is a potent NADThe Journal of biological chemistry · 2019
    Article
  15. Article
  16. High-altitude adaptation in humans: from genomics to integrative physiology.Journal of molecular medicine (Berlin, Germany) · 2017
    Review
  17. Review
  18. Poly(ADP-ribose) polymerase 1 is a novel target to promote axonal regeneration.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  19. Article
  20. Looking above but not beyond the genome for therapeutics in neurology and psychiatry: epigenetic proteins and RNAs find a new focus.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2013
    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

2 authors at 2 institutions in 1 country.

Brett LangleyThe Burke Medical Research Institute, 785 Mamaroneck Avenue, White Plains, NY, 10605, USA, blangley@burke.org.
Anthony Sauve
Burke Medical Research Institute · USCornell University · US

Funding

HDAC6: a target for regeneration following injury in the nervous systemR01NS071056 · NINDS · WINIFRED MASTERSON BURKE MED RES INST · PI LANGLEY, BRETT CAMERON · 2011 to 2015
$1.9M
Chemical Tools to Visualize Sirtuin Activity in CellsR21DK094001 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI SAUVE, ANTHONY A. · 2012 to 2013
$459k
NIDDK NIH HHS R21 DK094001NINDS NIH HHS NS071056NINDS NIH HHS R01 NS071056
6 · The paper itself

Abstract

Sirtuins are a conserved family of deacetylases whose activities are dependent on nicotinamide adenine dinucleotide (NAD+). Sirtuins act in different cellular compartments, such as the nucleus where they deacetylate histones and transcriptional factors, in the cytoplasm where they modulate cytoskeletal and signaling molecules, and in the mitochondria where they engage components of the metabolic machinery. Collectively, they tune metabolic processes to energy availability, and modulate stress responses, protein aggregation, inflammatory processes, and genome stability. As such, they have garnered much interest and have been widely studied in aging and age-related neurodegeneration. In this chapter, we review the identification of sirtuins and their biological targets. We focus on their biological mechanisms of action and how they might be regulated, including via NAD metabolism, transcriptional and posttranscriptional control, and as targets of pharmacological agents. Lastly, we highlight the numerous studies suggesting that sirtuins are efficacious therapeutic targets in neurodegenerative disease and injury.

Indexed as

Cell NucleusGene Expression RegulationGroup III Histone DeacetylasesHumansMitochondriaNervous System DiseasesSirtuinsGroup III Histone DeacetylasesSirtuins

Identifiers

PMID24037427
PMCPMC3805877
OpenAlexW2034589674

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.