Polymorphism in glutathione S-transferase loci as a risk factor for common cancers.

R C Strange, J T Lear, A A Fryer
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引用次数: 42

Abstract

Though a developing body of data indicates polymorphism at GST genes influences cancer susceptibility, it is unclear why a genotype is associated with one cancer but not another. We believe the GST exert a critical role in normal cell house-keeping activities. GSTM1, GSTM3 and GSTT1 influence tumorigenesis because these enzymes utilise the products of UV-induced oxidative stress. Further support for the importance of these genes in the protection of skin from UV comes from studies in systemic lupus erythematosus (Ollier et al, 1996). Thus, GSTM1 null is associated with increased anti-Ro (but not anti-La) antibodies, a phenotype associated with photosensitivity. At present there is no basis for predicting which cancers will be influenced by GST polymorphisms though other studies do indicate that the GSTs are critical in the metabolism of environmental carcinogens. For example, GSTT1 null confers an increased risk of astrocytoma (Hand et al, 1996). While brain tumours are not clearly associated with environmental pollutants, N-methyl-N-nitrosourea, processed meats and occupation have been implicated. Why GSTT1 but not GSTM1 or GSTM3 influences the risk of astrocytoma is unclear. GSTM3 appears a good susceptibility candidate, as some astrocytes demonstrate strong expression (Hand et al, 1996). Susceptibility to squamous cell cancer of the larynx, a pathology associated with chronic consumption of tobacco and alcohol, is also influenced by allelism at GSTM3 (Jahnke et al, 1996). The roles of CYP2D6 and CYP1A1 are even more unclear, though the finding that systemic agents such as arsenic predispose to multiple BCC, suggests that CYP2D6-mediated hepatic detoxification of photosensitizing agents may be important. Importantly, the extent of altered risk conferred by genotypes is generally 2-3 fold and it is necessary to identify which other genes interact with the GST so that haplotypes associated with 10-20 fold increases in risk can be defined.

谷胱甘肽s -转移酶位点多态性是常见癌症的危险因素。
尽管越来越多的数据表明GST基因的多态性影响癌症易感性,但尚不清楚为什么一种基因型与一种癌症相关,而与另一种癌症无关。我们认为GST在正常的细胞管理活动中发挥着关键作用。GSTM1、GSTM3和GSTT1影响肿瘤发生,因为这些酶利用了紫外线诱导的氧化应激的产物。对系统性红斑狼疮的研究进一步支持了这些基因在保护皮肤免受紫外线伤害方面的重要性(Ollier等,1996)。因此,GSTM1空值与抗ro(而非抗la)抗体增加有关,这是一种与光敏性相关的表型。虽然有研究表明GST在环境致癌物的代谢中起着至关重要的作用,但目前还没有预测GST多态性会影响哪些癌症的依据。例如,GSTT1缺失会增加星形细胞瘤的风险(Hand等,1996)。虽然脑肿瘤与环境污染物没有明确的联系,但n -甲基-n -亚硝基脲、加工肉类和职业都与之有关。为什么GSTT1而不是GSTM1或GSTM3影响星形细胞瘤的风险尚不清楚。GSTM3似乎是一个很好的易感性候选者,因为一些星形胶质细胞表现出强烈的表达(Hand等,1996)。喉部鳞状细胞癌(一种与长期吸烟和饮酒有关的病理)的易感性也受到GSTM3等位基因的影响(Jahnke et al, 1996)。CYP2D6和CYP1A1的作用更不清楚,尽管发现全身药物如砷易导致多发性BCC,表明CYP2D6介导的光敏药物的肝脏解毒可能很重要。重要的是,基因型所带来的风险改变程度通常为2-3倍,有必要确定哪些其他基因与GST相互作用,以便确定与风险增加10-20倍相关的单倍型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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