Cited by 669Advanced Glycation End Products researchGenetics, Aging, and Longevity in Model OrganismsPotato Plant Research

The DOI matches its Crossref record; 177 of the 179 references it cites were found in a registry or an index.

The Role of Advanced Glycation End Products in Aging and Metabolic Diseases: Bridging Association and Causality

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Abstract

Accumulation of advanced glycation end products (AGEs) on nucleotides, lipids, and peptides/proteins are an inevitable component of the aging process in all eukaryotic organisms, including humans. To date, a substantial body of evidence shows that AGEs and their functionally compromised adducts are linked to and perhaps responsible for changes seen during aging and for the development of many age-related morbidities. However, much remains to be learned about the biology of AGE formation, causal nature of these associations, and whether new interventions might be developed that will prevent or reduce the negative impact of AGEs-related damage. To facilitate achieving these latter ends, we show how invertebrate models, notably Drosophila melanogaster and Caenorhabditis elegans, can be used to explore AGE-related pathways in depth and to identify and assess drugs that will mitigate against the detrimental effects of AGE-adduct development.

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Crossref · 10.1016/j.cmet.2018.08.014

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Metadata

Authors
Chaudhuri, J., Bains, Y., Guha, S., Kahn, A., Hall, D., Bose, N., Gugliucci, A., & Kapahi, P.
Affiliations
  • Buck Institute for Research on Aging (US)
  • Touro University California (US)
Corresponding author
  • Chaudhuri, Jyotiska
  • Gugliucci, Alejandro
  • Kapahi, Pankaj
Venue
Cell Metabolism
Publisher
Elsevier BV
Published
2018-09
Volume
28
Issue
3
Pages
337-352
ISSN
1550-4131 (ISSN-L)
OpenAlex
W2892213316
Cited by
669
References
179
Citations by year
2026: 70 · 2025: 118 · 2024: 91 · 2023: 107 · 2022: 83 · 2021: 116 · 2020: 48 · 2019: 34 · 2018: 1
FWCI
6.44
Type
journal article
Language
en
Open access
Locations
  • Cell Metabolism (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • Touro Scholar (Touro College) (submittedVersion)
Funders
  • American Federation for Aging Research
  • Larry L. Hillblom Foundation
  • impact circle award
  • NIH (R21 AG053066, RO1 AG045835, RO1 5RO1HL113887)
  • Touro University California
  • NIH/NIA (T32 AG000266)
  • Hillblom Foundation Postdoctoral Fellowship
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Potato Plant Research
Keywords
advanced glycation end products, aging, metabolic disorders, AGE formation, age-related diseases, Drosophila melanogaster, Caenorhabditis elegans, invertebrate models, drug screening
MeSH terms
Aging, Animals, Drosophila melanogaster, Humans, Metabolic Diseases, Yeasts, Signal Transduction, Glycation End Products, Advanced, Caenorhabditis elegans, Oxidative Stress, Neurodegenerative Diseases, Models, Animal, Mice, Rats

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