Evidence map›Paper›PMID 35203320›Full record

ReviewCells2022

Epigenetic Regulation of Cellular Senescence.

Jack Crouch, Maria Shvedova, Rex Jeya Rajkumar Samdavid Thanapaul, Vladimir Botchkarev, Daniel Roh

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

77 citing papers in PubMed, 114 citations in OpenAlex.

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17 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

5 authors at 1 institution in 1 country.

Jack CrouchDivision of Plastic and Reconstructive Surgery, Department of Surgery, Boston University School of Medicine, Boston, MA 02118, USA.
Maria ShvedovaDivision of Plastic and Reconstructive Surgery, Department of Surgery, Boston University School of Medicine, Boston, MA 02118, USA.
Rex Jeya Rajkumar Samdavid ThanapaulDivision of Plastic and Reconstructive Surgery, Department of Surgery, Boston University School of Medicine, Boston, MA 02118, USA.
Vladimir BotchkarevDepartment of Dermatology, Boston University School of Medicine, Boston, MA 02118, USA.
Daniel RohDivision of Plastic and Reconstructive Surgery, Department of Surgery, Boston University School of Medicine, Boston, MA 02118, USA.
Boston University · US

Funding

Transposable elements in the keratinocyte genome and their regulation during skin development and epidermal differentiationR01AR078306 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BOTCHKAREV, VLADIMIR A, LAU, NELSON C · 2021 to 2025
$2.7M
Chromatin architectural protein CTCF and regulation of skin development and tumorigenesisR01AR071727 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BOTCHKAREV, VLADIMIR A, KOHWI-SHIGEMATSU, TERUMI · 2017 to 2021
$2.6M
DNA hydroxymethylation and Tet-enzymes in the control of the skin development and hair growthR01AR075776 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BOTCHKAREV, VLADIMIR A · 2019 to 2023
$1.8M
The skin of naked mole rats as a model for scar-free wound healingR33AR078093 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BOTCHKAREV, VLADIMIR A, GORBUNOVA, VERA · 2023 to 2023
$406k
Role of Senescence in the Impaired Wound Healing of AgingR03AG067983 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ROH, DANIEL SAM · 2020 to 2021
$330k
NIAMS NIH HHS R01 AR071727NIAMS NIH HHS R01 AR075776NIAMS NIH HHS R01 AR078306NIAMS NIH HHS R33 AR078093NIA NIH HHS R03 AG067983
6 · The paper itself

Abstract

Senescence is a complex cellular stress response that abolishes proliferative capacity and generates a unique secretory pattern that is implicated in organismal aging and age-related disease. How a cell transitions to a senescent state is multifactorial and often requires transcriptional regulation of multiple genes. Epigenetic alterations to DNA and chromatin are powerful regulators of genome architecture and gene expression, and they play a crucial role in mediating the induction and maintenance of senescence. This review will highlight the changes in chromatin, DNA methylation, and histone alterations that establish and maintain cellular senescence, alongside the specific epigenetic regulation of the senescence-associated secretory phenotype (SASP).

Indexed as

Cellular SenescenceEpigenesis, GeneticChromatinHistonesChromatinHistonesagingDNA methylationepigeneticshistone modificationSASPsenescence

Identifiers

PMID35203320
PMCPMC8870565
OpenAlexW4213310651

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.