Evidence map›Paper›PMID 42073386›Full record

ArticleLife (Basel, Switzerland)2026

UVA Irradiation Promotes ROS-Mediated Formation of the Common Deletion in Mitochondrial DNA.

Gabriele A Fontana, Navnit K Singh, Nadezhda Rotankova, Antonia Eichelberg, Michela Di Filippo, Michael R MacArthur, Susanne Heldmaier, Franziska Wandrey, Hans-Dietmar Beer, Shana J Sturla and 1 more

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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

11 authors.

Gabriele A FontanaDepartment of Health Sciences and Technology, ETH Zurich, Schmelzbergstrasse 9, 8092 Zurich, Switzerland.ORCID 0000-0001-7697-6833
Navnit K SinghDepartment of Health Sciences and Technology, ETH Zurich, Schmelzbergstrasse 9, 8092 Zurich, Switzerland.ORCID 0009-0007-1837-144X
Nadezhda RotankovaDepartment of Health Sciences and Technology, ETH Zurich, Schmelzbergstrasse 9, 8092 Zurich, Switzerland.ORCID 0009-0001-7066-3235
Antonia EichelbergDepartment of Health Sciences and Technology, ETH Zurich, Schmelzbergstrasse 9, 8092 Zurich, Switzerland.
Michela Di FilippoDepartment of Dermatology, University Hospital Zurich, 8952 Schlieren, Switzerland.
Michael R MacArthurDepartment of Health Sciences and Technology, ETH Zurich, Schmelzbergstrasse 9, 8092 Zurich, Switzerland.ORCID 0000-0003-3593-6995
Susanne HeldmaierMibelle Group, 5033 Buchs, Switzerland.
Franziska WandreyMibelle Group Biochemistry, 5033 Buchs, Switzerland.ORCID 0000-0002-1296-4021
Hans-Dietmar BeerDepartment of Dermatology, University Hospital Zurich, 8952 Schlieren, Switzerland.ORCID 0000-0002-8085-713X
Shana J SturlaDepartment of Health Sciences and Technology, ETH Zurich, Schmelzbergstrasse 9, 8092 Zurich, Switzerland.ORCID 0000-0001-6808-5950
Hailey L GahlonDepartment of Health Sciences and Technology, ETH Zurich, Schmelzbergstrasse 9, 8092 Zurich, Switzerland.ORCID 0000-0003-4388-2798

Funding

Federation of Migros CooperativesInnosuisse
6 · The paper itself

Abstract

Ultraviolet (UV) radiation from the sun causes adverse skin changes such as premature aging. UV-induced mitochondrial DNA (mtDNA) alterations, including deletions, contribute to photoaging and cellular dysfunction. While the most frequent mtDNA rearrangement is the common deletion (CD), characterized by the loss of nearly one-third of the genome (4977 bp), detailed knowledge of mechanisms governing UV-mediated initiation of the CD and mitigation strategies are lacking. Here, we investigated how increasing UV exposure increases CD levels in human skin fibroblasts via cellular reactive oxygen species (ROS) formation and mtDNA oxidation and demonstrated that antioxidant preconditioning of cells prevents UVA-induced CD accumulation. Conversely, UVB exposure induced cyclobutane pyrimidine dimers (CPDs) without affecting ROS, suggesting an ROS-independent pathway. Using a 3D full-thickness human skin model, we confirmed UVA-dependent CD formation in both the epidermis and dermis. RNA-Seq analysis of UVA-exposed fibroblasts revealed upregulation of mitochondrial DNA replication genes and downregulation of mtDNA repair genes. These findings provide insight into how UVA and UVB differ in detrimental effects on mtDNA, with UVA impacting mtDNA maintenance and transcription via a ROS-dependent mechanism, and provide a physiologically relevant platform to evaluate potential interventions.

Indexed as

mitochondrial DNA deletionphotoagingreactive oxygen species

Identifiers

PMID42073386
PMCPMC13117788

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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.