Istituto Dermopatico dell'Immacolata, Clinical Epidemiology Unit, IDI-IRCCS, Rome, Italy.
Acta Derm Venereol. 2011 May;91(3):284-9. doi: 10.2340/00015555-1078.
Glutathione S-transferases (GSTs) are a family of enzymes that are known to play an important role in cellular protection against oxidative stress, including the oxidative stress caused by ultraviolet radiation. This study focused on the possible involvement of GSTM1 and GSTT1 polymorphisms in risk modulation of cutaneous melanoma. Within a case-control study, the presence of the null polymorphism at GSTM1 and GSTT1 was investigated in 188 cases of cutaneous melanoma and 152 controls. Information on socio-demographic characteristics, medical history, sun exposure and pigmentary characteristics were collected for all subjects. Logistic regression was used to estimate odds ratio (OR) and 95% confidence intervals (CI). An interaction was suggested between the GSTM1 and GSTT1 "null" genotype and episodes of sunburn in childhood OR of interaction (1.65, 95% CI (95% CI) 0.27-9.94). The risk of melanoma among the subset of participants who reported sunburns in childhood and who had both null variants, was nine (OR 9.16; 95% CI 1.18-70.9). The results suggest that subjects carrying both GSTM1 and GSTT1 null polymorphisms and experiencing sunburns in childhood have an extremely high risk of melanoma.
谷胱甘肽 S-转移酶(GSTs)是一类酶,已知其在细胞对抗氧化应激(包括由紫外线辐射引起的氧化应激)中起着重要作用。本研究集中探讨 GSTM1 和 GSTT1 多态性在皮肤黑色素瘤风险调节中的可能作用。在病例对照研究中,在 188 例皮肤黑色素瘤病例和 152 例对照中研究了 GSTM1 和 GSTT1 缺失多态性的存在。对所有受试者收集了社会人口统计学特征、病史、日照和色素特征的信息。使用逻辑回归来估计比值比(OR)和 95%置信区间(CI)。提示 GSTM1 和 GSTT1“缺失”基因型与儿童期晒伤之间存在交互作用 OR 交互作用(1.65,95%CI(95%CI)0.27-9.94)。在报告儿童期晒伤且具有两种缺失变异体的参与者亚组中,黑色素瘤的风险为 9 倍(OR 9.16;95%CI 1.18-70.9)。结果表明,携带 GSTM1 和 GSTT1 缺失多态性且经历过儿童期晒伤的受试者患黑色素瘤的风险极高。