Evidence map›Paper›PMID 38391933›Full record

ReviewCells2024

Unraveling Histone Loss in Aging and Senescence.

Sushil Kumar Dubey, Rashmi Dubey, Mark Ellsworth Kleinman

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
5.8field-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

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Formaldehyde induces and promotes Alzheimer's disease pathologies in a 3D human neural cell culture model.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

3 authors at 1 institution in 1 country.

Sushil Kumar DubeyDepartment of Surgery, East Tennessee State University, Johnson City, TN 37614, USA.ORCID 0000-0001-8259-2908
Rashmi DubeyDepartment of Surgery, East Tennessee State University, Johnson City, TN 37614, USA.
Mark Ellsworth KleinmanDepartment of Surgery, East Tennessee State University, Johnson City, TN 37614, USA.ORCID 0000-0001-8557-7949
East Tennessee State University · US

Funding

The Role of Histone Deacetylases in Age-related Macular DegenerationR01EY028206 · NEI · UNIVERSITY OF KENTUCKY · PI KLEINMAN, MARK E · 2018 to 2022
$1.8M
Endothelial Cell Dysregulation in Neovascular AMDK08EY021757 · NEI · UNIVERSITY OF KENTUCKY · PI KLEINMAN, MARK E · 2011 to 2015
$1.6M
NEI NIH HHS K08 EY021757NEI NIH HHS R01 EY028206NIH HHS NIH K08EY021757NIH HHS NIH R01EY028206
6 · The paper itself

Abstract

As the global population experiences a notable surge in aging demographics, the need to understand the intricate molecular pathways exacerbated by age-related stresses, including epigenetic dysregulation, becomes a priority. Epigenetic mechanisms play a critical role in driving age-related diseases through altered gene expression, genomic instability, and irregular chromatin remodeling. In this review, we focus on histones, a central component of the epigenome, and consolidate the key findings of histone loss and genome-wide redistribution as fundamental processes contributing to aging and senescence. The review provides insights into novel histone expression profiles, nucleosome occupancy, disruptions in higher-order chromatin architecture, and the emergence of noncanonical histone variants in the aging cellular landscape. Furthermore, we explore the current state of our understanding of the molecular mechanisms of histone deficiency in aging cells. Specific emphasis is placed on highlighting histone degradation pathways in the cell and studies that have explored potential strategies to mitigate histone loss or restore histone levels in aging cells. Finally, in addressing future perspectives, the insights gained from this review hold profound implications for advancing strategies that actively intervene in modulating histone expression profiles in the context of cellular aging and identifying potential therapeutic targets for alleviating a multitude of age-related diseases.

Indexed as

ChromatinHistonesEpigenesis, GeneticNucleosomesChromatinHistonesNucleosomesagingepigeneticshistone degradationhistoneshistone variantnucleosome occupancysenescence

Identifiers

PMID38391933
PMCPMC10886805
OpenAlexW4391693024

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.