Zhu Youqing, Deng Changsheng, Zhang Youcai, Zhou Xin, He Xiaoling
Department of Gasteroenterology, Zhongnan Hospital, Wuhan University, Wuhan 430071, China.
Zhonghua Nei Ke Za Zhi. 2002 Aug;41(8):538-40.
To analyse the association genetic polymorphisms of glutathione S-transferase (GST) M1 and T1 with genetic susceptibility to sporadic colorectal adenocarcinoma (SCRAC).
All subjects are unrelated the Han people in Hubei province of China. Using multiple PCR, we studied the genetic polymorphisms of the GSTM1, GSTT1 genes of 101 healthy controls and 104 SCRAC patients.
(1) All the differences of the frequency of GSTM1 null genotype between SCRACs and the controls, between proximal and distal SCRACs and between the elder and the younger SCRACs did not reach statistical significance. (2) The differences of the frequency of GSTT1 null genotype between SCRACs and the controls did not reach statistical significance too; But the null genotype for GSTT1 was significantly more common among distal SCRACs when compared with the proximals (66.2%:44.4%, chi(2) = 3.97, P < 0.05) and more common among the elder SCRACs when compared with younger SCRACs (70.9%:49.0%, chi(2) = 5.21, P < 0.05). (3) Subjects carring both of the null genotypes for GSTM1 and GSTT1 had more than 4.33-fold risk for developing SCRACs compared with the subjects caring both of the nonull genotypes for GSTM1 and GSTT1 (OR = 4.33, 95% confidence interval, 1.56 - 12.04).
(1) There was no association the susceptibility to SCRAC with GSTM1 or GSTT1 null genotype alone, but the date suggests GSTT1 null genotype may influence the distal SCRAC, especially the elder; (2) The individual with both of the null genotypes of GSTM1 and GSTT1 increases markedly the risk of SCRAC, and this genotype is the susceptibility gene to SCRAC.
分析谷胱甘肽S-转移酶(GST)M1和T1基因多态性与散发性结直肠癌(SCRAC)遗传易感性的关系。
所有受试者均为中国湖北省无血缘关系的汉族人。采用多重聚合酶链反应(PCR),研究了101例健康对照者和104例SCRAC患者的GSTM1、GSTT1基因多态性。
(1)SCRAC患者与对照组之间、近端与远端SCRAC患者之间以及老年与年轻SCRAC患者之间,GSTM1基因缺失型频率的所有差异均未达到统计学意义。(2)SCRAC患者与对照组之间GSTT1基因缺失型频率的差异也未达到统计学意义;但与近端SCRAC患者相比,GSTT1基因缺失型在远端SCRAC患者中明显更常见(66.2%:44.4%,χ² = 3.97,P < 0.05),与年轻SCRAC患者相比,在老年SCRAC患者中更常见(70.9%:49.0%,χ² = 5.21,P < 0.05)。(3)与同时携带GSTM1和GSTT1基因非缺失型的受试者相比,同时携带GSTM1和GSTT1基因缺失型的受试者发生SCRAC的风险高出4.33倍以上(比值比 = 4.33,95%置信区间,1.56 - 12.04)。
(1)单独的GSTM1或GSTT1基因缺失型与SCRAC易感性无关,但数据表明GSTT1基因缺失型可能影响远端SCRAC,尤其是老年患者;(2)同时携带GSTM1和GSTT1基因缺失型的个体显著增加了SCRAC的风险,且该基因型是SCRAC的易感基因。