首页> 外文期刊>Pharmacogenetics >Single tube multiplex polymerase chain reaction genotype analysis of GSTM1, GSTT1 and GSTP1: relation of genotypes to TP53 tumor status and clinicopathological variables in breast cancer patients (published erratum appears in Pharmacogenetics 1999 Fe
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Single tube multiplex polymerase chain reaction genotype analysis of GSTM1, GSTT1 and GSTP1: relation of genotypes to TP53 tumor status and clinicopathological variables in breast cancer patients (published erratum appears in Pharmacogenetics 1999 Fe

机译:GSTM1,GSTT1和GSTP1的单管多重聚合酶链反应基因型分析:乳腺癌患者基因型与TP53肿瘤状态和临床病理变量的关系(发表的勘误载于Pharmacogenetics 1999 Fe

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摘要

Glutathione S-transferases are involved in the conjugation of a number of human carcinogens. The frequencies of the deletion alleles coding for GSTM1, and GSTT1, related to deficient conjugation of xenobiotics, as well as a recently reported variant in the exon 5 of GSTP1 were investigated in this study. A multiplex polymerase chain reaction based method for a rapid and high throughput genotype analysis of all three GSTM1, GSTT1 and GSTP1 genes in a single tube was developed. Leukocyte DNA from two hundred and thirty-nine (n = 239) breast cancer patients were genotyped. Tumors from a subset of these breast cancer patients (n = 131) have previously been investigated for mutations in the TP53 gene, levels of p53 protein accumulation and loss of heterozygosity at several loci on chromosome 17. When genetic alterations in the tumors were analyzed with respect to glutathione S-transferase genotypes, a significantly higher proportion of the patients with a G allele (GG + AG) of the GSTP1 had loss of heterozygosity at the TP53 gene locus mapping to 17p, compared with non-G allele carriers (74% versus 29%) (P = 0.018). The patients carrying the G allele of GSTP1 also had more frequently mutations in the TP53 gene in their tumor (38%), compared with patients with the AA genotype (21%) (P = 0.055). G allele carriers had predominantly deletion or transversion mutations in the TP53 gene (5 of 7 and 5 of 6 respectively). A higher frequency of the G allele carriers was observed among patients with negative lymph node status (P = 0.0004). A higher proportion of the patients with positive lymph node status at the time of diagnosis had a combined GSTM1 null/GSTT1 null genotype (P = 0.05). Patients who were homozygous for the deleted GSTM1 allele were found to have a significantly shorter overall survival (P = 0.036).
机译:谷胱甘肽S-转移酶参与许多人类致癌物的结合。在这项研究中,研究了编码与异种生物体结合不足有关的GSTM1和GSTT1缺失等位基因的频率,以及最近报道的GSTP1外显子5中的变异。开发了一种基于多重聚合酶链反应的方法,可在单个试管中对所有三个GSTM1,GSTT1和GSTP1基因进行快速且高通量的基因型分析。对239例(n = 239)乳腺癌患者的白细胞DNA进行了基因分型。先前已经研究了这些乳腺癌患者(n = 131)的一部分中的肿瘤的TP53基因突变,p53蛋白积累水平以及第17号染色​​体上几个基因座的杂合性丧失。就谷胱甘肽S-转移酶基因型而言,与非G等位基因携带者相比,具有GSTP1 G等位基因(GG + AG)的患者中TP53基因位点定位到17p的杂合性丧失比例更高(74%对比29%)(P = 0.018)。与具有AA基因型的患者(21%)相比,携带GSTP1 G等位基因的患者其肿瘤中TP53基因的突变也更为频繁(38%)(P = 0.055)。 G等位基因携带者在TP53基因中主要具有缺失或颠换突变(分别为7个中的5个和6个中的5个)。在淋巴结状态阴性的患者中,G等位基因携带者的频率更高(P = 0.0004)。诊断时淋巴结状态阳性的患者中,有较高比例的患者具有合并的GSTM1 null / GSTT1 null基因型(P = 0.05)。发现缺失的GSTM1等位基因纯合的患者的总生存期明显缩短(P = 0.036)。

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