Oral Diagnosis Department, Semiology and Oral Pathology Areas, Piracicaba Dental School, University of Campinas (UNICAMP), São Paulo, Brazil.
João de Barros, Barreto University Hospital (HUJBB), Federal University of Pará (UFPA), Pará, Brazil.
Histopathology. 2018 Jan;72(2):330-338. doi: 10.1111/his.13381. Epub 2017 Nov 3.
The aim of this study was to analyse allelic loss of the phosphatase and tensin homologue deleted on chromosome 10 (PTEN) gene and its protein immuno-expression in dysplastic oral lesions and oral squamous cell carcinomas (OSCCs).
Samples were collected from 153 patients [20 ranulas used as a control (C); 30 leucoplakias with mild dysplasia (MD); 30 leucoplakias with moderate to severe dysplasia (MSD); 73 oral squamous cell carcinoma (OSCC)]. PTEN protein expression was investigated using immunohistochemistry, and PTEN allelic loss was analysed by fluorescence in-situ hybridisation (FISH). Differences among groups were evaluated using the χ test. PTEN expression was higher in MSD (P = 0.002) and OSCC (P = 0.0259) compared with the C group; additionally, a higher expression was observed in MSD (P = 0.0035) and OSCC (P = 0.049) than MD. Regarding FISH analysis, a higher hemizygous (single copy) loss was observed in OSCC than in C (P = 0.0467) and in OSCC than in MD (P = 0.0175), as well as a higher homozygous deletion in OSCC compared with C (P = 0.0159) and OSCC than MD (P = 0.0145).
The results of this work suggest that PTEN allelic loss is an important mechanism in the late stage of the development of oral potentially malignant lesions into oral cancer.
本研究旨在分析 10 号染色体缺失的磷酸酶和张力蛋白同源物(PTEN)基因的等位基因缺失及其在发育不良性口腔病变和口腔鳞状细胞癌(OSCC)中的蛋白免疫表达。
从 153 名患者中采集样本[20 例口外型舌下囊肿用作对照(C);30 例轻度发育不良的口腔白斑(MD);30 例中重度发育不良的口腔白斑(MSD);73 例口腔鳞状细胞癌(OSCC)]。使用免疫组织化学法检测 PTEN 蛋白表达,并用荧光原位杂交(FISH)分析 PTEN 等位基因缺失。用卡方检验评估组间差异。MSD(P=0.002)和 OSCC(P=0.0259)组的 PTEN 表达高于 C 组;MSD(P=0.0035)和 OSCC(P=0.049)组的表达也高于 MD 组。关于 FISH 分析,OSCC 组的杂合性(单拷贝)缺失率高于 C 组(P=0.0467)和 MD 组(P=0.0175),OSCC 组的纯合性缺失率也高于 C 组(P=0.0159)和 MD 组(P=0.0145)。
本研究结果表明,PTEN 等位基因缺失是口腔潜在恶性病变发展为口腔癌的晚期的重要机制。