Evidence map›Paper›PMID 42033084›Full record

ArticleAging cell2026

Diminished and Altered Cellular Senescence Response in Delayed Wound Healing of Aging.

Maria Shvedova, Rex Jeya Rajkumar Samdavid Thanapaul, Qiaoling Wang, Grace Haeun Shin, Jannat Dhillon, Daniel Sam Roh

Abstract read
In one paragraph

Article in Aging cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Maria ShvedovaDepartment of Surgery, Division of Plastic and Reconstructive Surgery, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0001-7071-8753
Rex Jeya Rajkumar Samdavid ThanapaulDepartment of Surgery, Division of Plastic and Reconstructive Surgery, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0002-5760-9437
Qiaoling WangDepartment of Surgery, Division of Plastic and Reconstructive Surgery, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Grace Haeun ShinDepartment of Surgery, Division of Plastic and Reconstructive Surgery, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Jannat DhillonDepartment of Surgery, Division of Plastic and Reconstructive Surgery, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.
Daniel Sam RohDepartment of Surgery, Division of Plastic and Reconstructive Surgery, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0002-5288-2805

Funding

Targeting Senescence to Improve Wound Healing in AgingK76AG083300 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Daniel Sam Roh · 2023 to 2026
$972k
Role of Senescence in the Impaired Wound Healing of AgingR03AG067983 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI ROH, DANIEL SAM · 2020 to 2021
$330k
NIA NIH HHS K76 AG083300NIA NIH HHS K76AG083300NIA NIH HHS R03 AG067983NIA NIH HHS R03AG067983
6 · The paper itself

Abstract

The transient upregulation of cellular senescence within wound tissues has been demonstrated to be an important biological process facilitating efficient tissue repair. Dysregulation of this transient wound-induced senescence response can result in impaired healing outcomes. Given the established age-related decline in tissue regenerative capacity, we hypothesized that alterations in this senescence response contribute to the delayed healing of cutaneous wounds in aged individuals. Our investigation demonstrated a significant delay in the closure of full-thickness dorsal skin wounds in aged mice compared to their young counterparts. Analysis of the wound microenvironment revealed a transient upregulation of senescence-associated markers (p16, p21, senescence-associated β-galactosidase) and senescence-associated secretory phenotype factors in the wound tissue of young mice, a response that was markedly attenuated in aged mice. Single-cell RNA sequencing analysis of all cells isolated from day 6 wounds identified a distinct population of p16

Indexed as

AgingCellular SenescenceWound HealingAnimalsFibroblastsHumansMaleMiceMice, Inbred C57BLagingmicep16p21SASPsenescencewound healing

Identifiers

PMID42033084
PMCPMC13109648

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.