Evidence map›Paper›PMID 35599179›Full record

ReviewTrends in cell biology2023

The heterogeneity of cellular senescence: insights at the single-cell level.

Rachel L Cohn, Nathan S Gasek, George A Kuchel, Ming Xu

Abstract readReview
In one paragraph

Review in Trends in cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers.

0numbers the graph read from it
0cells of the map it votes in
172citing 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

172 citing papers in PubMed.

  1. Article
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  4. Anti-aging effects of glycyrrhizin via maintaining Klotho levels.Journal of clinical biochemistry and nutrition · 2026
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112 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

4 authors.

Rachel L CohnUConn Center on Aging, UConn Health, Farmington, CT, USA; Department of Genetics and Genome Sciences, UConn Health, Farmington, CT, USA.
Nathan S GasekUConn Center on Aging, UConn Health, Farmington, CT, USA; Department of Genetics and Genome Sciences, UConn Health, Farmington, CT, USA.
George A KuchelUConn Center on Aging, UConn Health, Farmington, CT, USA.
Ming XuUConn Center on Aging, UConn Health, Farmington, CT, USA; Department of Genetics and Genome Sciences, UConn Health, Farmington, CT, USA. Electronic address: mixu@uchc.edu.

Funding

The KAPP-Sen Tissue Mapping Center CollaborativeU54AG075941 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI GAROVIC, VESNA D, KUCHEL, GEORGE A · 2021 to 2025
$13.8M
The Jackson Laboratory Senescence Tissue Mapping Center (JAX-Sen TMC) - Data Analysis CoreU54AG079753 · NIA · JACKSON LABORATORY · PI ROSENTHAL, NADIA A · 2022 to 2025
$11.0M
Translational Geroscience NetworkR33AG061456 · NIA · MAYO CLINIC ROCHESTER · PI JAMES L. KIRKLAND, STEPHEN B. KRITCHEVSKY · 2019 to 2026
$6.2M
Reciprocal Modulation of the Microbiome and Cellular Senescence in Metabolic DysfunctionR01AG068860 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI XU, MING, ZHOU, YANJIAO · 2020 to 2024
$2.8M
Targeting p21-Highly Expressing Cells to Increase Lifespan and Healthspan in Old AgeR01AG076642 · NIA · UNIVERSITY OF MINNESOTA · PI Ming Xu · 2022 to 2026
$2.4M
Targeting p21-positive Senescent Cells in vivo for Alleviating Metabolic and Physical DysfunctionR01AG066679 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI XU, MING · 2020 to 2024
$2.2M
The UConn/JAX-GM Training Program in Genomic ScienceT32HG010463 · NHGRI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Mark D ADAMS, Christine R Beck · 2020 to 2026
$1.5M
Role of Senolytics in Lower Urinary Tract Aging and Voiding DisordersR21AG063528 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KUCHEL, GEORGE A, SMITH, PHILLIP PAUL · 2019 to 2020
$440k
Targeting P21-Highly-Expressing Senescent Cells In Vivo for Improving Cognitive Function in the Alzheimers DiseasesR03AG072374 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI XU, MING · 2021 to 2022
$328k
NHGRI NIH HHS T32 HG010463NIA NIH HHS R01 AG066679NIA NIH HHS R01 AG068860NIA NIH HHS R01 AG076642NIA NIH HHS R03 AG072374NIA NIH HHS R21 AG063528NIA NIH HHS R33 AG061456NIA NIH HHS U54 AG075941NIA NIH HHS U54 AG079753
6 · The paper itself

Abstract

Senescent cells are highly associated with aging and pathological conditions and could be targeted to slow the aging process. One commonly used marker to examine senescent cells in vivo is p16, which has led to important discoveries. Recent studies have also described new senescence markers beyond p16 and have highlighted the importance of investigating senescence heterogeneity in cell types and tissues. With the development of high-throughput technologies, such as single-cell RNA-seq and single-nucleus RNA-seq, we can examine senescent cells at the single-cell level and potentially uncover new markers. This review emphasizes that there is an urgent need to investigate senescence heterogeneity and discuss how this could be accomplished by using advanced technologies and sequencing datasets.

Indexed as

AgingCellular SenescenceHumansagingp16p21RNA-sequencingsenolytics

Identifiers

PMID35599179
PMCPMC9812642

What OpenQuestion holds

Textmetadata
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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.