Cited by 403Skin Protection and Agingmelanin and skin pigmentationDermatologic Treatments and Research

Photoaging of human skin

Open access
Berneburg, M., Plettenberg, H., Krutmann, J.·2000·Photodermatology, Photoimmunology & Photomedicine

Abstract

Chronic sun exposure causes photoaging of human skin, a process that is characterized by clinical, histological and biochemical changes which differ from alterations in chronologically aged but sun‐protected skin. Within recent years, substantial progress has been made in unraveling the underlying mechanisms of photoaging. Induction of matrix metalloproteinases as a consequence of activator protein (AP)‐1 and nuclear factor (NF)‐κB activation as well as mutations of mitochondrial DNA have been identified recently. This has increased our understanding of photoaging significantly and has led to new prophylactic and therapeutic strategies aimed at the prevention and repair of the detrimental effects of chronic sun‐exposure on the skin.

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Registry

Crossref · 10.1034/j.1600-0781.2000.160601.x

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47 of 47 references verified0 citation errors · 0 not checkable

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  • People with darker skin commonly have delayed and less extensive signs of photoaging as opposed to people with lighter skin.

    “Due to these factors, people who have darker skin commonly have delayed and signs of photoaging to a lesser extent as opposed to people who have lighter skin [55].”

    From A Comprehensive Review of the Role of UV Radiation in Photoaging Processes Between Different Types of Skin (2025) · cites this paper as [55]

    The Photobiology section says that people with darker skin show clinical signs of photoaging much later than fair-skinned people, and explains that melanin protects skin cells from UV exposure. It does not specifically say that their signs are less extensive, so that part of the claim is not established by our copy. (LLM, conf=0.84)

    Experimental — accuracy not yet measured
  • Reactive oxygen species produced by UV rays cause damage to DNA, proteins, and lipids, causing disturbances in cellular function and aiding in premature aging of skin.

    “Reactive oxygen species (ROS) that are produced by UV rays cause damage to DNA, proteins, and lipids, causing disturbances in cellular function and aiding in the premature aging of skin [55].”

    From A Comprehensive Review of the Role of UV Radiation in Photoaging Processes Between Different Types of Skin (2025) · cites this paper as [55]

    The Photobiology section says UVA generates ROS that cause lipid peroxidation and DNA-strand breaks, while the Photoprotection section says oxidative stress plays a major role in photoaging. The cited passages do not establish ROS-mediated protein damage, so the full list of damaged molecules is not supported. (LLM, conf=0.87)

    Experimental — accuracy not yet measured
  • Exposure to UV radiation leads to an increase in oxidative stress, which leads to cellular damage.

    “Being exposed to UV radiation leads to an increase in oxidative stress, which leads to cellular damage.”

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Authors
Berneburg, M., Plettenberg, H., & Krutmann, J.
Affiliations
Heinrich Heine University Düsseldorf (DE)
Venue
Photodermatology, Photoimmunology & Photomedicine
Publisher
Wiley
Published
2000-12
Volume
16
Issue
6
Pages
239-244
ISSN
  • 0905-4383 (ISSN-L)
  • 1600-0781
OpenAlex
W2045031994
Cited by
403
References
47
Citations by year
2026: 9 · 2025: 20 · 2024: 18 · 2023: 15 · 2022: 40 · 2021: 14 · 2020: 15 · 2019: 19 · 2018: 22 · 2017: 16 · 2016: 23 · 2015: 24 · 2014: 24 · 2013: 13 · 2012: 12
FWCI
1.43
Type
journal article
Language
en
Open access
Locations
  • Photodermatology Photoimmunology & Photomedicine (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • European Commission
  • Bundesministerium für Bildung und Forschung
Topics
  • Health Sciences › Medicine › Dermatology › Skin Protection and Aging
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
  • Health Sciences › Medicine › Dermatology › Dermatologic Treatments and Research
Keywords
photoaging, chronic sun exposure, skin aging, matrix metalloproteinases, activator protein-1, nuclear factor-kappaB, mitochondrial DNA mutations, skin histology, skin biochemistry
MeSH terms
DNA, Mitochondrial, Humans, Skin, Sunlight, Ultraviolet Rays, Skin Aging, Matrix Metalloproteinases

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