Variants at the OCA2/HERC2 locus affect time to first cutaneous squamous cell carcinoma in solid organ transplant recipients collected using two different study designs

Summary Background Variants at the oculocutaneous albinism 2 (OCA2)/HECT and RLD domain containing E3 ubiquitin protein ligase 2 (HERC2) locus have been associated with pigmentation phenotypes and risk of developing several types of skin cancer. Objectives To evaluate OCA2/HERC2 locus variants for t...

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Bibliographic Details
Published in:British journal of dermatology (1951) 2017-10, Vol.177 (4), p.1066-1073
Main Authors: Wei, L., Allain, D.C., Bernhardt, M.N., Gillespie, J.L., Peters, S.B., Iwenofu, O.H., Nelson, H.H., Arron, S.T., Toland, A.E.
Format: Article
Language:English
Subjects:
Albinism
Alleles
Animal models
Deoxyribonucleic acid
DNA
Eye
Genome-wide association studies
Genomes
Genotyping
Health risk assessment
Medical records
Pigmentation
Skin cancer
Squamous cell carcinoma
Studies
Ubiquitin
Ubiquitin-protein ligase
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Summary:Summary Background Variants at the oculocutaneous albinism 2 (OCA2)/HECT and RLD domain containing E3 ubiquitin protein ligase 2 (HERC2) locus have been associated with pigmentation phenotypes and risk of developing several types of skin cancer. Objectives To evaluate OCA2/HERC2 locus variants for their impact on time to develop cutaneous squamous cell carcinoma (cSCC) in organ transplant recipients (OTRs) who are at elevated risk of developing cSCC. Methods Participants were solid OTRs ascertained from two centres (n = 125 and 261) with an average of 13·1 years of follow‐up post‐transplant. DNA was available for genotyping for all participants, in addition to medical records and questionnaire data. The Ohio State University study had a case–control design with prospective follow‐up, and the University of California San Francisco study was a national cross‐sectional survey with retrospective chart review. Results OCA2 variants rs12913832 and rs916977 were significantly associated with time to first cSCC post‐transplant. OTRs homozygous for the brown‐eye alleles of rs916977 (GG) and rs12913832 (AA) had significant delays of time to first cSCC post‐transplant compared with individuals homozygous for the blue‐eye alleles (hazard ratio 0·34, P < 0·001 and hazard ratio 0·54, P = 0·012, respectively). Both variants were highly associated with eye colour in the combined studies (P < 0·001). Conclusions This study is the first to show an association between OCA2/HERC2 variants and time to first cSCC post‐transplant. This may impact dermatological screening recommendations for high‐risk populations. What's already known about this topic? Variants in pigment‐related genes have been found to be associated with increased risk of skin cancer through both candidate gene and genome‐wide association studies. Blue‐eye‐associated alleles at the HERC2/OCA2 locus have associated with increased risk of cutaneous squamous cell carcinoma (cSCC) in immunocompetent populations in candidate gene and genome‐wide association studies. What does this study add? This study shows that blue‐eye‐associated variants of rs12913832 and rs916977, at the HERC2/OCA2 locus, are associated with decreased time to first cSCC post‐transplant in solid organ transplant recipients. What is the translational message? These results have potential implications for the development of screening recommendations and risk models for cSCC in organ transplant recipients. Linked Comment: Nguyen et al. Br J Dermato
ISSN:0007-0963
1365-2133
DOI:10.1111/bjd.15618