Li Qin, Wang Lingrong, Chen Yanlin, Du Yinghua, Kong Ping, Li Yufen, Xu Xiaoqun
Department of Otorhinolaryngology, Linyi People's Hospital of Shandong, Linyi, 276003, China.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Dec;23(24):1105-7, 1111.
To study the relationship between genetic polymorphisms of GSTM1 GSTT1 and the susceptibility of laryngeal and hypopharyngeal carcinomas (LHC).
The GSTM1 and GSTT1 genotypes were determined by multiplex PCR analysis in 76 LHC patients and 76 population controls. The association between the genotypes and LHC risk was measured by odds ratios (ORs) and 95% confidence intervals (95% CIs).
The frequency of GSTM1 null genotype was 59.2% in the LHC patients and 42.1% in controls (OR=1.935, 95% CI=1.069-3.510), the difference was significant (P<0.01). The frequency of GSTT1 null genotype was 57.9% in the LHC patients and 51.3% in controls. The difference was not significant (P>0.05). In smokers, the risk of the LHC increased in subjects of GSTM1 null genotype (OR=5.545, 95% CI=2.158-13.528).
GSTM1 polymorphisms are associated with susceptibility to the LHC. It has the synergistic effects with smoking in the development of the LHC. GSTT1 genotypes might have no association with risk of the LHC in urban Linyi.
研究谷胱甘肽硫转移酶M1(GSTM1)和谷胱甘肽硫转移酶T1(GSTT1)基因多态性与喉癌和下咽癌(LHC)易感性之间的关系。
采用多重聚合酶链反应分析方法,对76例LHC患者和76名人群对照者进行GSTM1和GSTT1基因分型。通过比值比(OR)和95%置信区间(95%CI)来衡量基因型与LHC风险之间的关联。
LHC患者中GSTM1缺失基因型的频率为59.2%,对照组为42.1%(OR=1.935,95%CI=1.069-3.510),差异有统计学意义(P<0.01)。LHC患者中GSTT1缺失基因型的频率为57.9%,对照组为51.3%,差异无统计学意义(P>0.05)。在吸烟者中,GSTM1缺失基因型个体发生LHC的风险增加(OR=5.545,95%CI=2.158-13.528)。
GSTM1基因多态性与LHC易感性相关,在LHC发生过程中与吸烟具有协同作用。在临沂市城区,GSTT1基因型可能与LHC风险无关。