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Systematic review on gene–sun exposure interactions in skin cancer

BACKGROUND: The risk of skin cancer is determined by environmental factors like ultraviolet radiation (UVR), personal habits like time spent outdoors and genetic factors. This review aimed to survey existing studies in gene–environment (GxE) interaction on skin cancer risk, and report on GxE effect...

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Autores principales: Shraim, Rasha, Farran, Mohamed Ziad, He, George, Marunica Karsaj, Jelena, Zgaga, Lina, McManus, Ross
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568388/
https://www.ncbi.nlm.nih.gov/pubmed/37537768
http://dx.doi.org/10.1002/mgg3.2259
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author Shraim, Rasha
Farran, Mohamed Ziad
He, George
Marunica Karsaj, Jelena
Zgaga, Lina
McManus, Ross
author_facet Shraim, Rasha
Farran, Mohamed Ziad
He, George
Marunica Karsaj, Jelena
Zgaga, Lina
McManus, Ross
author_sort Shraim, Rasha
collection PubMed
description BACKGROUND: The risk of skin cancer is determined by environmental factors like ultraviolet radiation (UVR), personal habits like time spent outdoors and genetic factors. This review aimed to survey existing studies in gene–environment (GxE) interaction on skin cancer risk, and report on GxE effect estimates. METHODS: We searched Embase, Medline (Ovid) and Web of Science (Core Collection) and included only primary research that reported on GxE on the risk of the three most common types of skin cancer: basal cell carcinoma (BCC), squamous cell carcinoma (SCC) and melanoma. Quality assessment followed the Newcastle–Ottawa Scale. Meta‐analysis was not possible because no two studies examined the same interaction. This review was registered on PROSPERO (CRD42021238064). RESULTS: In total 260 records were identified after exclusion of duplicates. Fifteen studies were included in the final synthesis—12 used candidate gene approach. We found some evidence of GxE interactions with sun exposure, notably, with MC1R, CAT and NOS1 genes in melanoma, HAL and IL23A in BCC and HAL and XRCC1 in SCC. CONCLUSION: Sun exposure seems to interact with genes involved in pigmentation, oxidative stress and immunosuppression, indicating that excessive UV exposure might exhaust oxidative defence and repair systems differentially, dependent on genetic make‐up. Further research is warranted to better understand skin cancer epidemiology and develop sun exposure recommendations. A genome‐wide approach is recommended as it might uncover unknown disease pathways dependent on UV radiation.
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spelling pubmed-105683882023-10-13 Systematic review on gene–sun exposure interactions in skin cancer Shraim, Rasha Farran, Mohamed Ziad He, George Marunica Karsaj, Jelena Zgaga, Lina McManus, Ross Mol Genet Genomic Med Review Article BACKGROUND: The risk of skin cancer is determined by environmental factors like ultraviolet radiation (UVR), personal habits like time spent outdoors and genetic factors. This review aimed to survey existing studies in gene–environment (GxE) interaction on skin cancer risk, and report on GxE effect estimates. METHODS: We searched Embase, Medline (Ovid) and Web of Science (Core Collection) and included only primary research that reported on GxE on the risk of the three most common types of skin cancer: basal cell carcinoma (BCC), squamous cell carcinoma (SCC) and melanoma. Quality assessment followed the Newcastle–Ottawa Scale. Meta‐analysis was not possible because no two studies examined the same interaction. This review was registered on PROSPERO (CRD42021238064). RESULTS: In total 260 records were identified after exclusion of duplicates. Fifteen studies were included in the final synthesis—12 used candidate gene approach. We found some evidence of GxE interactions with sun exposure, notably, with MC1R, CAT and NOS1 genes in melanoma, HAL and IL23A in BCC and HAL and XRCC1 in SCC. CONCLUSION: Sun exposure seems to interact with genes involved in pigmentation, oxidative stress and immunosuppression, indicating that excessive UV exposure might exhaust oxidative defence and repair systems differentially, dependent on genetic make‐up. Further research is warranted to better understand skin cancer epidemiology and develop sun exposure recommendations. A genome‐wide approach is recommended as it might uncover unknown disease pathways dependent on UV radiation. John Wiley and Sons Inc. 2023-08-03 /pmc/articles/PMC10568388/ /pubmed/37537768 http://dx.doi.org/10.1002/mgg3.2259 Text en © 2023 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Shraim, Rasha
Farran, Mohamed Ziad
He, George
Marunica Karsaj, Jelena
Zgaga, Lina
McManus, Ross
Systematic review on gene–sun exposure interactions in skin cancer
title Systematic review on gene–sun exposure interactions in skin cancer
title_full Systematic review on gene–sun exposure interactions in skin cancer
title_fullStr Systematic review on gene–sun exposure interactions in skin cancer
title_full_unstemmed Systematic review on gene–sun exposure interactions in skin cancer
title_short Systematic review on gene–sun exposure interactions in skin cancer
title_sort systematic review on gene–sun exposure interactions in skin cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568388/
https://www.ncbi.nlm.nih.gov/pubmed/37537768
http://dx.doi.org/10.1002/mgg3.2259
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