Mohr Lawrence C, Rodgers J Keith, Silvestri Gerard A
Department of Medicine, Department of Biometry and Epidemiology, Environmental Biosciences Program, Medical University of South Carolina, 135 Cannon Street, Suite 405, P.O. Box 250838, Charleston, South Carolina 29425, USA.
Anticancer Res. 2003 May-Jun;23(3A):2111-24.
Glutathione S-transferases (GSTs) are a family of enzymes that detoxify hydrophobic electrophiles, including polycyclic aromatic hydrocarbon carcinogens that have been implicated in the pathogenesis of lung cancer. The GSTM1 gene within the mu class of human GSTs has been shown to be polymorphic, with individuals who are homozygous for a null allele having the GSTM1-null genotype. Individuals with the GSTM1-null genotype are deficient in both the GSTM1 and GSTM3 isoenzymes in the lung. A number of epidemiological studies have been conducted to assess the association between the GSTM1-null genotype and the risk of lung cancer. Although there have been conflicting reports regarding this relationship, the current weight of evidence indicates that the GSTM1-null genotype is probably associated with a modest increase in the risk of lung cancer. This risk appears to be greater in African-American and Asian populations than in Caucasians. Recent investigations have shown that the GSTM1-null genotype combined with CYP1A1, NAT2, or GSTP1 polymorphisms confers a greater risk of lung cancer than the GSTM1-null genotype alone. Future investigations should focus on assessing the risk of lung cancer related to multiple combinations of genetic polymorphisms that may identify individuals who are at high risk for developing lung cancer with a greater degree of certainty than is currently possible. This could lead to new clinical strategies for counseling, risk reduction and the detection of lung at an early and potentially curable stage.
谷胱甘肽S-转移酶(GSTs)是一类可使疏水性亲电试剂解毒的酶,这些亲电试剂包括与肺癌发病机制有关的多环芳烃致癌物。人类GSTs μ类中的GSTM1基因已被证明具有多态性,纯合缺失等位基因的个体具有GSTM1缺失基因型。GSTM1缺失基因型的个体肺部的GSTM1和GSTM3同工酶均缺乏。已经进行了多项流行病学研究来评估GSTM1缺失基因型与肺癌风险之间的关联。尽管关于这种关系的报道相互矛盾,但目前的证据表明,GSTM1缺失基因型可能与肺癌风险的适度增加有关。这种风险在非裔美国人和亚洲人群中似乎比在白种人中更大。最近的研究表明,与单独的GSTM1缺失基因型相比,GSTM1缺失基因型与CYP1A1、NAT2或GSTP1多态性相结合会带来更大的肺癌风险。未来的研究应集中于评估与基因多态性多种组合相关的肺癌风险,这可能比目前更确定地识别出患肺癌高风险个体。这可能会带来新的临床策略,用于咨询、降低风险以及在早期和可能治愈阶段检测肺癌。