Preudhomme C, Nisse C, Hebbar M, Vanrumbeke M, Brizard A, Lai J L, Fenaux P
Inserm U124, Institut de Recherche sur le Cancer de Lille, France.
Leukemia. 1997 Sep;11(9):1580-2. doi: 10.1038/sj.leu.2400767.
Glutathione S transferase theta 1 (GSTT1) is implicated in the detoxification of different substances, including carcinogens. Recently, an increased incidence of GSTT1 null genotype was found in myelodysplastic syndromes (MDS) by comparison with a control population. We analyzed GSTT1 gene by PCR in 174 MDS cases and 100 controls. The incidence of GSTT1 null genotype was 22% in MDS in 19% in controls (P = 0.53). The incidence of GSTT1 null genotype in MDS did not differ according to gender, FAB classification, karyotype and whether MDS were therapy related or 'de novo'. In 86 of the de novo cases, data on previous occupational and environmental exposure to a list of 170 substances were available. In those MDS patients, a significantly lower frequency of GSTT1 null genotype was seen in cases with previous jobs exposed to chemicals, and with previous exposure to mineral dusts and exhaust gases. A lower frequency (but with only borderline significance) was seen in MDS patients who had been coal miners and those who had been exposed to any of the 70 substances analyzed. Overall, GSTT1 null genotype occurred at a similar incidence (19%) in controls and in MDS cases previously exposed to any substance, but tended to be higher in unexposed MDS patients (40%, P = 0.07). Our results do not confirm the higher incidence of GSTT1 null genotype observed in MDS. The lower incidence of GSTT1 null genotype in MDS cases exposed to some compounds previously found associated with MDS is apparently unexpected. However, it could be explained by the fact that GSTT1 enzyme, which has a detoxification role for some compounds, could also have an activating role for other substances, including solvents.
谷胱甘肽S转移酶θ1(GSTT1)参与包括致癌物在内的多种物质的解毒过程。最近,与对照人群相比,骨髓增生异常综合征(MDS)中GSTT1基因缺失型的发生率有所增加。我们采用聚合酶链反应(PCR)分析了174例MDS患者和100例对照者的GSTT1基因。MDS患者中GSTT1基因缺失型的发生率为22%,对照者为19%(P = 0.53)。MDS患者中GSTT1基因缺失型的发生率在性别、FAB分型、核型以及MDS是否与治疗相关或“原发性”方面并无差异。在86例原发性病例中,有关于既往职业和环境暴露于170种物质的相关数据。在这些MDS患者中,既往有化学物质暴露工作史、既往有矿物粉尘和废气暴露史的患者,GSTT1基因缺失型的频率显著较低。在曾为煤矿工人以及曾暴露于所分析的70种物质中的任何一种的MDS患者中,也观察到较低的频率(但仅具有临界显著性)。总体而言,对照者和既往有任何物质暴露史的MDS病例中,GSTT1基因缺失型的发生率相似(19%),但在未暴露的MDS患者中往往更高(40%,P = 0.07)。我们的结果并未证实MDS中观察到的GSTT1基因缺失型发生率更高。MDS病例中GSTT1基因缺失型在先前发现与MDS相关的某些化合物暴露情况下发生率较低,这显然出乎意料。然而,这可以用以下事实来解释:GSTT1酶对某些化合物具有解毒作用,但对包括溶剂在内的其他物质也可能具有激活作用。