Biochemistry Laboratory, Farhat Hached University Hospital, Sousse, Tunisia.
Med Oncol. 2014 Jan;31(1):760. doi: 10.1007/s12032-013-0760-z. Epub 2013 Nov 20.
In this study, we investigated the associations of polymorphisms in glutathione-S-transferases (GSTs) genes that are GSTM1, GSTT1, and GSTP1, with sporadic colorectal cancer (CRC). Hundred and fifty patients with CRC and 128 healthy controls were genotyped. DNA was isolated from blood samples. Polymorphisms were assessed by polymerase chain reaction-restriction fragment length polymorphism-based methods and polymerase chain reaction multiplex. Logistic regression analyses showed significant risk for CRC associated with GSTP1 homozygotes for Val-105 (OR 4.82; 95 % CI 1.97-11.80) or for individuals who possessed at least one Val-105 allele (OR 2.54; 95 % CI 1.751-3.703). There were no statistically significant differences in the frequency of GSTM1- and GSTT1-null genotypes (p > 0.05). The GSTM1-null was found in 70.47 % of all cases and 70.07 % of controls (OR 0.61; 95 % CI 0.33-1.12). The GSTT1-null genotype was found in 38.77 % of cases and 49.22 % of controls (OR 1.53; 95 % CI 0.94-2.47). No effect of any genotype for GSTM1 and GSTT1 on CRC was detected. But then an association between the polymorphism of the GSTP1 and the CRC susceptibility was detected.
在这项研究中,我们研究了谷胱甘肽-S-转移酶(GSTs)基因的多态性与散发性结直肠癌(CRC)的关联,这些基因包括 GSTM1、GSTT1 和 GSTP1。我们对 150 名 CRC 患者和 128 名健康对照者进行了基因分型。从血液样本中提取 DNA。采用聚合酶链反应-限制性片段长度多态性和聚合酶链反应多重方法评估多态性。逻辑回归分析显示,GSTP1 纯合子 Val-105 或至少携带一个 Val-105 等位基因的个体与 CRC 的发生存在显著相关性(OR 4.82;95%CI 1.97-11.80)。GSTM1 和 GSTT1 缺失基因型的频率无统计学差异(p>0.05)。所有病例和对照组中,GSTM1 缺失的发生率分别为 70.47%和 70.07%(OR 0.61;95%CI 0.33-1.12)。病例组和对照组中 GSTT1 缺失基因型的发生率分别为 38.77%和 49.22%(OR 1.53;95%CI 0.94-2.47)。未检测到 GSTM1 和 GSTT1 任何基因型对 CRC 的影响。但随后检测到 GSTP1 多态性与 CRC 易感性之间存在关联。