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    <responseDate>2026-10-15T21:59:49Z</responseDate>
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                <identifier>oai:data.mendeley.com/3m6ywf2xt5.1</identifier>
                <datestamp>2026-05-08T06:55:44Z</datestamp>
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    <dc:creator>Rocha, Lilian</dc:creator>
    <dc:title>Genomic Evidence for Imiquimod-Mediated Clearance of Mutated Skin in Xeroderma Pigmentosum</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>In this study, we performed whole-exome sequencing of paired pre- and post-treatment biopsies from XP patients and demonstrated a consistent and substantial reduction in detectable somatic mutational burden following imiquimod therapy. We further characterized mutational signatures, showing persistence of oxidative damage–associated patterns in XP-V patients. Importantly, no tumors developed in treated areas during 24 months of follow-up.
To our knowledge, this is the first in vivo human study to evaluate the genomic impact of imiquimod using whole-exome sequencing and mutational signature analysis. These findings provide novel molecular insight into the effects of field-directed therapy and contribute to the understanding of cutaneous field cancerization in high-risk populations.
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    <dc:subject>Clinical Health</dc:subject>
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    <dc:identifier>doi:10.17632/3m6ywf2xt5.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/3m6ywf2xt5.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:date>2026-05-08T06:55:44Z</dc:date>
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