4.6 Article

UVA Radiation, DNA Damage, and Melanoma

Journal

ACS OMEGA
Volume 7, Issue 37, Pages 32936-32948

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.2c04424

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Funding

  1. NIH [CA228089]

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Melanoma, a lethal skin tumor, is linked to sunlight exposure. UVB radiation plays a significant role in melanoma formation, while the potential role of UVA radiation needs further investigation.
Melanoma is a lethal type of skin tumor that has been linked with sunlight exposure chiefly in fair-skinned human populations. Wavelengths from the sun that can reach the earth's surface include UVA radiation (320-400 nm) and UVB radiation (280-320 nm). UVB effectively induces the formation of dimeric DNA photoproducts, preferentially the cyclobutane pyrimidine dimers (CPDs). The characteristic UVB signature mutations in the form of C to T mutations at dipyrimidine sequences are prevalent in melanoma tumor genomes and have been ascribed to deamination of cytosines within CPDs before DNA polymerase bypass. However, evidence from epidemiological, animal, and other experimental studies also suggest that UVA radiation may participate in melanoma formation. The DNA damage relevant for UVA includes specific types of CPDs at TT sequences and perhaps oxidative DNA damage to guanine, both induced by direct or indirect, photosensitization-mediated chemical and biophysical processes. We summarize the evidence for a potential role of UVA in melanoma and discuss some of the mechanistic pathways of how UVA may induce mutagenesis in melanocytes.

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