Evidence map›Paper›PMID 37998258›Full record

ArticleJournal of burn care & research : official publication of the American Burn Association2024

Feeling the Heat. Mapping the Epigenetic Modifications of Histone during Burn Wound Healing.

Larissa S A Rolim, Patricia da S Nascente, Rogerio M Castilho, Cristiane H Squarize

Open access · hybridAbstract read
In one paragraph

Article in Journal of burn care & research : official publication of the American Burn Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. A scATAC-seq atlas of stasis zone in rat skin burn injury wound process.Frontiers in cell and developmental biology · 2024
    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

4 authors at 2 institutions in 2 countries.

Larissa S A RolimDepartment of Periodontics and Oral Medicine, Laboratory of Epithelial Biology, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-6274-5134
Patricia da S NascenteDepartment of Periodontics and Oral Medicine, Laboratory of Epithelial Biology, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-3137-4107
Rogerio M CastilhoDepartment of Periodontics and Oral Medicine, Laboratory of Epithelial Biology, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0001-5358-612X
Cristiane H SquarizeDepartment of Periodontics and Oral Medicine, Laboratory of Epithelial Biology, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-6782-3429
University of Michigan · USUniversidade Federal de Pelotas · BR

Funding

Modulating the PI3K Pathway During the Managing of Wound Contracture and Accelerated Healing - Equipment SupplementR01GM120056 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CASTILHO, ROGERIO MORAES, SQUARIZE, CRISTIANE · 2017 to 2021
$2.0M
Combined bioprinting with stem cell technology to regenerate skin burn woundsR01GM143938 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BOTTINO, MARCO C, CASTILHO, ROGERIO MORAES · 2021 to 2024
$2.0M
NIGMS NIH HHS R01 GM120056NIGMS NIH HHS R01GM120056NIGMS NIH HHS R01 GM143938
6 · The paper itself

Abstract

Burn injuries are observed throughout a wide range of ages, with over 1.1 million Americans suffering burns yearly, and half of these require hospitalization. Epigenetic modifications are fast-acting mechanisms that allow the human body to respond and adapt to environmental changes, including burn injuries. There is a lack of understanding of the epigenetic role during burn-induced tissue repair. Here, we characterize the histone modifications that follow burn injury, aiming at future pharmacological intervention using drugs capable of targeting epigenetic events. A clinically relevant porcine burn model was used to recapitulate the skin healing process after the burn. Isolated skin tissues at different time points were used to detect the acetylation levels of histones H3K27, H4K5, H4K8, and H4K12 as significant players of gene transcription using MetaXpress High-Content Imaging Analysis. We observed that the acetylation of histones is dynamically adjusted throughout healing, and its modifications are uniquely expressed according to the anatomical location and time of healing. We also observed that histone H4K5 is the most widely expressed during healing, followed by histone H3K27. We observed that histones expressed in intact skin tissue adjacent to the burn site could sense the burn injury by changing its histone acetylation pattern compared to control skin from uninjured and distant skin. Using a clinically relevant animal model, we have generated a comprehensive landscape of epigenetic modifications during burn healing. Our data will help us identify novel epi-drugs capable of manipulating histone modifications during healing to accelerate the healing process.

Indexed as

BurnsHistonesAnimalsEpigenesis, GeneticHot TemperatureHumansSwineWound HealingHistonesburn woundchromatin remodelingepigeneticporcinetissue regeneration

Identifiers

PMID37998258
PMCPMC10911690
OpenAlexW4388969543

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.