Cited by 286DNA Repair MechanismsGenetics, Aging, and Longevity in Model OrganismsMetabolism, Diabetes, and Cancer

DNA damage response and metabolic disease

Open access
Shimizu, Ippei, Yoshida, Yohko, Suda, Masayoshi, Minamino, Tohru·2014·Cell Metabolism

Abstract

Accumulation of DNA damage has been linked to the process of aging and to the onset of age-related diseases including diabetes. Studies on progeroid syndromes have suggested that the DNA damage response is involved in regulation of metabolic homeostasis. DNA damage could impair metabolic organ functions by causing cell death or senescence. DNA damage also could induce tissue inflammation that disturbs the homeostasis of systemic metabolism. Various roles of molecules related to DNA repair in cellular metabolism are being uncovered, and such molecules could also have an impact on systemic metabolism. This review explores mechanisms by which the DNA damage response could contribute to metabolic dysfunction.

Integrity signals

Registry

Crossref · 10.1016/j.cmet.2014.10.008

Cites

137 of 137 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Cites

Flagged first, then by citations

1 of the 138 references couldn’t be matched to a known paper.

Cited by

Sorted by citations

Authors
Shimizu, I., Yoshida, Y., Suda, M., & Minamino, T.
Affiliations
  • Niigata University (JP)
  • Japan Science and Technology Agency (JP)
Corresponding author
Minamino, Tohru
Venue
Cell Metabolism
Publisher
Elsevier BV
Published
2014-12
Volume
20
Issue
6
Pages
967-977
ISSN
1550-4131 (ISSN-L)
OpenAlex
W2048777894
Cited by
286
References
138
Citations by year
2026: 15 · 2025: 33 · 2024: 36 · 2023: 29 · 2022: 32 · 2021: 24 · 2020: 25 · 2019: 29 · 2018: 25 · 2017: 12 · 2016: 18 · 2015: 7 · 2012: 1
FWCI
1.16
Type
journal article
Language
en
Open access
Locations
  • Cell Metabolism (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Japan Diabetes Foundation
  • Ministry of Education, Culture, Sports, Science and Technology
  • Takeda Medical Research Foundation
  • Takeda Science Foundation
  • Ono Medical Research Foundation
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
Keywords
DNA damage response, metabolic disorders, aging, age-related diseases, diabetes mellitus, progeroid syndromes, metabolic homeostasis, cellular senescence, cell death, tissue inflammation, DNA repair, systemic metabolism
MeSH terms
Animals, DNA Damage, DNA Repair, Humans, Metabolic Diseases

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review