Barroso Duarte Eliza Carla, Da Silva Marina Sena Lopes, Gomez Marcus Vinicius, Gomez Ricardo Santiago
Department of Oral Pathology and Surgery, School of Dentistry, Universidade Federal de Minas Gerais, Brazil.
Anticancer Res. 2006 Jan-Feb;26(1A):427-30.
Considering that tobacco is the main etiological factor in oral cancer and that oral leukoplakia is the most prevalent potentially malignant lesion, together with the fact that GSTT1 polymorphism increases the risk of oral squamous cell carcinoma, the purpose of this study was to investigate the GSTT1 null polymorphism and the risk of oral leukoplakia in individuals with tobacco smoking habits in a Brazilian population.
The GSTT1 genotypes of 72 tobacco smoking patients with oral leukoplakia and 72 tobacco smoking healthy subjects were studied by PCR-based methods.
The frequency of the GSTT1 null genotype in the group with oral leukoplakia (48.6%) was statistically different from the controls (27.8%). After stratification, the frequencies of the null genotype in female patients, lesions with absent/mild grade of dysplasia and from low-risk sites were statistically different from the control.
The GSTT1 null genotype may increase the risk of developing oral leukoplakia.
鉴于烟草是口腔癌的主要病因,口腔白斑是最常见的潜在恶性病变,同时谷胱甘肽S-转移酶T1(GSTT1)基因多态性会增加口腔鳞状细胞癌的风险,本研究旨在调查巴西有吸烟习惯人群中GSTT1基因缺失多态性与口腔白斑风险之间的关系。
采用基于聚合酶链反应(PCR)的方法,对72例有吸烟习惯的口腔白斑患者和72例有吸烟习惯的健康受试者的GSTT1基因型进行研究。
口腔白斑组中GSTT1基因缺失基因型的频率(48.6%)与对照组(27.8%)相比,差异具有统计学意义。分层分析后发现,女性患者、发育异常程度为无/轻度的病变以及低风险部位的病变中,GSTT1基因缺失基因型的频率与对照组相比差异具有统计学意义。
GSTT1基因缺失基因型可能会增加患口腔白斑的风险。