Acar Hasan, Ozturk Kayhan, Muslumanoglu M Hamza, Yildirim M Selman, Cora Tulin, Cilingir Oguz, Ozer Bedri
Department of Medical Genetics, Selçuk University, Meram Medical Faculty, Vali Izzet Pasa Caddesi, Konya 42090, Turkey.
Cancer Genet Cytogenet. 2006 Sep;169(2):89-93. doi: 10.1016/j.cancergencyto.2005.12.007.
The purpose of the present study was to investigate GSTM1 and GSTT1 genotypes by using multiplex polymerase chain reaction (PCR) in patients with laryngeal squamous cell carcinoma (LSCC). The genotypes of 110 patients with LSCC and of 197 healthy subjects as the control group were determined by PCR analysis for GSTM1 and GSTT1 genes. Results showed that frequencies of GSTM1-null, GSTT1-null, and both GSTs-null genotypes were 51.8, 30, and 16.4%, respectively, in the patients with LSCC and 37.6, 15.7, and 5.6% in the control group. There was a significant difference between the genotype distributions of all GSTs in patients and in control groups (P < 0.05). The results support the hypothesis that null genotypes of GSTM1 and GSTT1 can reduce detoxification capacity of GSTs as members of the xenobiotic enzyme system. GSTM1-null, GSTT1-null, and both GSTs-null genotypes were more common in the patients with LSCC than in the control group. Patients with both GSTs-null genotypes had the highest risk for supraglottic LSCC in the early period, even if they were light-to-medium smokers. Investigation and determination of the genetic basis of LSCC may contribute to detection of risk groups and to prevent LSCC in the population.
本研究的目的是通过多重聚合酶链反应(PCR)来调查喉鳞状细胞癌(LSCC)患者的GSTM1和GSTT1基因型。通过对GSTM1和GSTT1基因进行PCR分析,确定了110例LSCC患者和197名健康受试者作为对照组的基因型。结果显示,LSCC患者中GSTM1缺失、GSTT1缺失以及两种谷胱甘肽S-转移酶(GSTs)均缺失基因型的频率分别为51.8%、30%和16.4%,而对照组中分别为37.6%、15.7%和5.6%。患者组和对照组中所有GSTs的基因型分布存在显著差异(P < 0.05)。这些结果支持以下假设:作为外源性酶系统成员的GSTM1和GSTT1缺失基因型可降低GSTs的解毒能力。GSTM1缺失、GSTT1缺失以及两种GSTs均缺失基因型在LSCC患者中比在对照组中更常见。即使是轻度至中度吸烟者,两种GSTs均缺失基因型的患者在早期发生声门上型LSCC的风险最高。对LSCC遗传基础的调查和确定可能有助于检测风险群体并预防人群中的LSCC。