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PXD037726-1

PXD037726 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleDifferent biological effects of exposure to far-UVC (222 nm) and near-UVC (254 nm) irradiation
DescriptionUltraviolet C (UVC) light has long been used as a sterilizing agent, primarily through devices that emit at 254 nm. Depending on the dose and duration of exposure, UV 254 nm can cause erythema and photokeratitis and potentially cause skin cancer since it directly modifies nitrogenated nucleic acid bases. Filtered KrCl excimer lamps (emitting mainly at 222 nm) have emerged as safer germicidal tools and have even been proposed as devices to sterilize surgical wounds. All the studies that showed the safety of 222 nm analyzed cell number and viability, erythema generation, epidermal thickening, the formation of genetic lesions such as cyclobutane pyrimidine dimers (CPDs) and pyrimidine-(6-4)-pyrimidone photoproducts (6-4PPs) and cancer-inducing potential. Although nucleic acids can absorb and be modified by both UV 254 nm and UV 222 nm equally, compared to UV 254 nm, UV 222 nm is more intensely absorbed by proteins (especially aromatic side chains), causing photooxidation and cross-linking. Here, in addition to analyzing DNA lesion formation, for the first time, we evaluated changes in the proteome and cellular pathways, reactive oxygen species formation, and metalloproteinase (MMP) levels and activity in full-thickness in vitro reconstructed human skin (RHS) exposed to UV 222 nm. We also performed the longest (40 days) in vivo study of UV 222 nm exposure in the HRS/J mouse model at the occupational threshold limit value (TLV) for indirect exposure (25 mJ/cm2) and evaluated overall skin morphology, cellular pathological alterations, CPD and 6-4PP formation and MMP-9 activity. Our study showed that processes related to reactive oxygen species and inflammatory responses were more altered by UV 254 nm than by UV 222 nm. Our chronic in vivo exposure assay using the TLV confirmed that UV 222 nm causes minor damage to the skin. However, alterations in pathways related to skin regeneration raise concerns about direct exposure to UV 222 nm
HostingRepositoryPRIDE
AnnounceDate2026-02-05
AnnouncementXMLSubmission_2026-02-05_08:01:44.508.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterAdriana Franco Paes Leme
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606;
ModificationListmonohydroxylated residue; iodoacetamide derivatized residue
InstrumentLTQ Orbitrap Velos
Dataset History
RevisionDatetimeStatusChangeLog Entry
02022-10-26 01:03:41ID requested
12026-02-05 08:01:45announced
Publication List
10.1016/j.jphotobiol.2023.112713;
Tavares RSN, Adamoski D, Girasole A, Lima EN, da Silva Justo-Junior A, Domingues R, Silveira ACC, Marques RE, de Carvalho M, Ambrosio ALB, Leme AFP, Dias SMG, nm) irradiation. J Photochem Photobiol B, 243():112713(2023) [pubmed]
Keyword List
submitter keyword: UVC, irradiation, skin, germicidal lamp, hairless mice
Contact List
Adriana Franco Paes Leme
contact affiliationCoordenadora do laboratório de espectrometria de massas, LNBio, CNPEM, Brasil.
contact emailadriana.paesleme@lnbio.cnpem.br
lab head
Adriana Franco Paes Leme
contact affiliationCNPEM
contact emailadriana.paesleme@lnbio.cnpem.br
dataset submitter
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Dataset FTP location
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