Shraim Rasha, Farran Mohamed Ziad, He George, Marunica Karsaj Jelena, Zgaga Lina, McManus Ross
Department of Public Health and Primary Care, Institute of Population Health, Trinity College Dublin, Dublin, Ireland.
Department of Clinical Medicine, Trinity Translational Medicine Institute, Trinity College Dublin, Dublin, Ireland.
Mol Genet Genomic Med. 2023 Oct;11(10):e2259. doi: 10.1002/mgg3.2259. Epub 2023 Aug 3.
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.
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).
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.
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.
皮肤癌风险由紫外线辐射(UVR)等环境因素、户外停留时间等个人习惯以及遗传因素决定。本综述旨在调查基因 - 环境(GxE)相互作用对皮肤癌风险的现有研究,并报告GxE效应估计值。
我们检索了Embase、Medline(Ovid)和Web of Science(核心合集),仅纳入了报告GxE与三种最常见皮肤癌类型风险关系的原发性研究:基底细胞癌(BCC)、鳞状细胞癌(SCC)和黑色素瘤。质量评估遵循纽卡斯尔 - 渥太华量表。由于没有两项研究检验相同的相互作用,因此无法进行荟萃分析。本综述已在PROSPERO(CRD42021238064)上注册。
排除重复记录后,共识别出260条记录。最终纳入综合分析的有15项研究,其中12项采用候选基因方法。我们发现了一些GxE与日晒相互作用的证据,特别是在黑色素瘤中与MC1R、CAT和NOS1基因相互作用,在BCC中与HAL和IL23A基因相互作用,在SCC中与HAL和XRCC1基因相互作用。
日晒似乎与参与色素沉着、氧化应激和免疫抑制的基因相互作用,这表明过度紫外线暴露可能会根据基因组成差异耗尽氧化防御和修复系统。有必要进一步研究以更好地理解皮肤癌流行病学并制定日晒建议。建议采用全基因组方法,因为它可能揭示依赖紫外线辐射的未知疾病途径。