Evidence map›Paper›PMID 31981461›Full record

ArticleAging cell2020

Tissue specificity of senescent cell accumulation during physiologic and accelerated aging of mice.

Matthew J Yousefzadeh, Jing Zhao, Christina Bukata, Erin A Wade, Sara J McGowan, Luise A Angelini, Michael P Bank, Aditi U Gurkar, Collin A McGuckian, Mariah F Calubag and 4 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 220 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
220citing papers in PubMed, 1 pooled it
20.4field-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

220 citing papers in PubMed, 1 synthesis or guideline pooled it, 307 citations in OpenAlex.

  1. Pooled it
  2. Biomarkers of Cellular Senescence Predict the Onset of Mobility Disability and Are Reduced by Physical Activity in Older Adults.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Trial
  3. Article
  4. Rhenium-Based β-Galactosidase Probe Allows Senescence Profiling by Mass Cytometry.Angewandte Chemie (International ed. in English) · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Cellular senescence and aging: molecular mechanisms and convergent pathways.Cellular and molecular life sciences : CMLS · 2026
    Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review

160 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

14 authors at 2 institutions in 1 country.

Matthew J YousefzadehInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, USA.
Jing ZhaoDepartment of Molecular Medicine, Scripps Research Institute, Jupiter, FL, USA.
Christina BukataDepartment of Molecular Medicine, Scripps Research Institute, Jupiter, FL, USA.
Erin A WadeDepartment of Molecular Medicine, Scripps Research Institute, Jupiter, FL, USA.
Sara J McGowanInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, USA.
Luise A AngeliniInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, USA.
Michael P BankDepartment of Molecular Medicine, Scripps Research Institute, Jupiter, FL, USA.
Aditi U GurkarDepartment of Molecular Medicine, Scripps Research Institute, Jupiter, FL, USA.
Collin A McGuckianInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, USA.
Mariah F CalubagDepartment of Molecular Medicine, Scripps Research Institute, Jupiter, FL, USA.
Jonathan I KatoDepartment of Molecular Medicine, Scripps Research Institute, Jupiter, FL, USA.
Christin E BurdDepartments of Molecular Genetics and Cancer Biology and Genetics, The Ohio State University, Columbus, OH, USA.ORCID 0000-0002-7919-3954
Paul D RobbinsInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, USA.
Laura J NiedernhoferInstitute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0002-1074-1385
Scripps Research Institute · USCancer Genetics (United States) · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller · 1998 to 2026
$100.4M
Targeting Cellular Senescence to Extend HealthspanP01AG062413 · NIA · MAYO CLINIC ROCHESTER · PI Sundeep Khosla, Nathan K LeBrasseur · 2019 to 2026
$28.7M
VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Caterina Rosano · 2004 to 2026
$28.6M
Validation and characterization of the identified variants associated with human longevity in mouse modelsU19AG056278 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI JAN VIJG · 2017 to 2026
$24.5M
PROTEOMICSP01AG043376 · NIA · UNIVERSITY OF MINNESOTA · PI ROBBINS, PAUL D. · 2013 to 2019
$11.2M
Using the senolytic fisetin to suppress mortality in aged mice acutely exposed to murine beta-coronavirusR01AG063543 · NIA · UNIVERSITY OF MINNESOTA · PI NIEDERNHOFER, LAURA JANE · 2019 to 2023
$3.4M
Marital quality and longevity: Biobehavioral pathwaysR01AG057032 · NIA · OHIO STATE UNIVERSITY · PI KIECOLT-GLASER, JANICE · 2017 to 2021
$3.2M
Impact of senescence on T-cell function and immunotherapeutic responseR01AG059711 · NIA · OHIO STATE UNIVERSITY · PI BURD, CHRISTIN E · 2018 to 2022
$2.1M
Modulators of DNA damage associated nucleo-mitochondrial communication in agingR00AG049126 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GURKAR, ADITI U · 2017 to 2019
$835k
Immune cells as a driver of cell non-autonomous agingR56AG059676 · NIA · UNIVERSITY OF MINNESOTA · PI NIEDERNHOFER, LAURA JANE · 2018 to 2018
$385k
Modulators of DNA damage associated nucleo-mitochondrial communication in agingK99AG049126 · NIA · SCRIPPS FLORIDA · PI GURKAR, ADITI U · 2015 to 2016
$203k
NCI NIH HHS P30 CA077598NIA NIH HHS K99 AG049126NIA NIH HHS P01 AG043376NIA NIH HHS P01 AG062413NIA NIH HHS P30 AG024827NIA NIH HHS R00 AG049126NIA NIH HHS R00 AG057032NIA NIH HHS R01 AG057032NIA NIH HHS R01 AG059711NIA NIH HHS R01 AG063543NIA NIH HHS R56 AG059676NIA NIH HHS U19 AG056278
6 · The paper itself

Abstract

Senescent cells accumulate with age in vertebrates and promote aging largely through their senescence-associated secretory phenotype (SASP). Many types of stress induce senescence, including genotoxic stress. ERCC1-XPF is a DNA repair endonuclease required for multiple DNA repair mechanisms that protect the nuclear genome. Humans or mice with reduced expression of this enzyme age rapidly due to increased levels of spontaneous, genotoxic stress. Here, we asked whether this corresponds to an increased level of senescent cells. p16

Indexed as

AgingAnimalsCellular SenescenceCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsDNA DamageDNA RepairEndonucleasesFemaleLungMaleMiceMice, Inbred C57BLMice, TransgenicOrgan SpecificityCdkn1a protein, mouseCdkn2a protein, mouseCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsEndonucleasesErcc1 protein, mouseRNA, Messengeragingcellular senescenceDNA repairendogenous DNA damageERCC1-XPFprogeria

Identifiers

PMID31981461
PMCPMC7059165
OpenAlexW3002676854

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.