Cited by 759Telomeres, Telomerase, and SenescenceGenetics, Aging, and Longevity in Model OrganismsNuclear Structure and Function

The DOI matches its Crossref record; 208 of the 208 references it cites were found in a registry or an index; 200 of the 257 sources its claims cite were checked for support.

Telomere dysfunction in ageing and age-related diseases

Open access
Rossiello, Francesca, Jurk, Diana, Passos, João F., d’Adda di Fagagna, Fabrizio·2022·Nature Cell Biology

Abstract

Ageing organisms accumulate senescent cells that are thought to contribute to body dysfunction. Telomere shortening and damage are recognized causes of cellular senescence and ageing. Several human conditions associated with normal ageing are precipitated by accelerated telomere dysfunction. Here, we systematize a large body of evidence and propose a coherent perspective to recognize the broad contribution of telomeric dysfunction to human pathologies. Rossiello et al. review the contributions of telomere shortening and/or dysfunction to ageing and a broad spectrum of age-associated human diseases.

Overview

Integrity signals

Registry

Crossref · 10.1038/s41556-022-00842-x

Cites

208 of 208 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Verification

Claims the paper makes

67 Supported · 63 Partly supported · 32 No full text of the sources · 16 Own interpretation · 9 Supported so far · 2 Mixed support · 1 Couldn’t confirm · 1 Sources not found · 1 Not checked yet · 1 No basis given · accuracy not yet measured

Show all 130 claims

  • It may state two separate claims as one. 61
  • Probably not a substantial claim. 5
63 of 63
  • The paper relies on this without support.

    DNA is the only irreplaceable component of the cell.

    “the notion that DNA is the only irreplaceable component of the cell makes a strong argument in favour of an apical role of DNA integrity in ageing”
  • The paper relies on this without support.

    Leukocyte telomere length reflects telomere length or dysfunction in the relevant tissue or organ.

    “In a limited cohort, patients with atherosclerosis bear shorter telomeres in circulating leukocytes than healthy age-matched individuals114.”
  • The paper relies on this without support.

    Findings from mouse models of telomere dysfunction can be generalized to human age-related disease mechanisms.

    “A causal role of short and dysfunctional telomeres in cardiac diseases has been established in mice110.”
  • The paper relies on this without support.

    Clearance or senolytic elimination of senescent cells acts specifically by removing senescent cells and not through other mechanisms.

    “The clearance of senescent cells in aged mice improves heart functions and reduces the fraction of TAF-positive cardiomyocytes without a significant effect on mean telomere length36.”
  • The paper relies on this without support.

    Senescence markers such as p16, p21, and DDR activation indicate cellular senescence.

    “Chondrocytes, the cells that constitute the articular cartilage, show several senescence markers, including DDR activation, in osteoarthritis119,120.”
  • The paper relies on this without support.

    Telomere-associated foci indicate telomere dysfunction.

    “During physiological ageing in humans and mice, TAFs occur independently from telomere length in post-mitotic cardiomyocytes.”
  • The authors state this as an assumption.

    Mouse telomere biology differs from human telomere biology in ways relevant to translating therapies.

    “Of course, the different telomere biology of mice, the most commonly used animal model, with longer telomeres and widespread telomerase expression, compared with humans has to be considered when translating any potential therapy to the clinic.”
7 of 7

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Metadata

Authors
Rossiello, F., Jurk, D., Passos, J. F., & d’Adda di Fagagna, F.
Affiliations
  • IFOM (IT)
  • Mayo Clinic (US)
Corresponding author
Passos, João F.
Venue
Nature Cell Biology
Published
2022-02
Volume
24
Issue
2
Pages
135-147
ISSN
  • 1465-7392 (ISSN-L)
  • 1476-4679
OpenAlex
W4213091566
Cited by
754
References
208
Citations by year
2026: 142 · 2025: 231 · 2024: 203 · 2023: 140 · 2022: 36
FWCI
20.98
Type
journal article
Language
en
Open access
Locations
  • Nature Cell Biology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • Ted Nash Long Life Foundation
  • European Commission (2014‐2020, HORIZON2020, POR FESR 2014-2020, 825575)
  • Associazione Italiana per la Ricerca sul Cancro (5×1000, 21762, 21091)
  • Regione Lombardia (POR FESR 20142020, 2014–2020, FESR 2014-2020)
  • Fondazione Regionale per la Ricerca Biomedica (825575)
  • National Institutes of Health (UL1TR002377)
  • Biotechnology and Biological Sciences Research Council (BB/K017314/1)
  • European Regional Development Fund (FESR 2014-2020, 2014-2020’, POR FESR 2014-2020)
  • National Institute on Aging (R01AG068182, R01AG068048, P01AG062413)
  • National Cancer Institute (UH3CA268103, UG3CA268103)
  • National Institute of Diabetes and Digestive and Kidney Diseases (P30DK084567)
  • National Center for Advancing Translational Sciences
  • H2020 European Research Council (835103, 875139)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
Keywords
telomere dysfunction, telomere shortening, cellular senescence, aging, age-related diseases, senolytics, telomere damage
MeSH terms
Noncommunicable Diseases, Age Factors, Aging, Animals, DNA Damage, Humans, Telomere, Cellular Senescence, Telomere Homeostasis, Telomere Shortening

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