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人端粒酶催化亚基基因的重新表达是口腔癌发生过程中的早期事件。

Human telomerase catalytic subunit gene re-expression is an early event in oral carcinogenesis.

作者信息

Luzar B, Poljak M, Marin I J, Eberlinc A, Klopcic U, Gale N

机构信息

Institute of Microbiology & Immunology, University of Ljubljana, Slovenia.

出版信息

Histopathology. 2004 Jul;45(1):13-9. doi: 10.1111/j.1365-2559.2004.01892.x.

Abstract

AIMS

Detection of telomerase catalytic subunit (hTERT) mRNA has been used as a surrogate marker for estimation of telomerase activity. The exact role and timing of telomerase re-activation, a key enzyme implicated in cellular immortalization and transformation, in the multistep process of oral carcinogenesis is still unknown. The aim was to test the hypothesis that (i) quantitative rather than qualitative differences exist in the level of hTERT mRNA expression between normal oral mucosa, different grades of oral epithelial abnormalities and squamous cell carcinomas of the oral cavity, and that (ii) hTERT gene re-expression is an important, probably early event in oral carcinogenesis.

METHODS AND RESULTS

The relative quantity of hTERT mRNA was analysed in 45 frozen oral epithelia representing different morphological stages of oral carcinogenesis classified according to the Ljubljana classification and in 37 oral squamous cell carcinomas, using a commercially available LightCycler Telo TAGGG hTERT Quantification kit. hTERT mRNA was not detected in normal or reactive hyperplastic oral epithelia, but was present in 43% of atypical hyperplasias (premalignant lesions), 60% of intraepithelial carcinomas and 68% of oral squamous cell carcinomas. Statistical analysis revealed two groups of oral epithelial changes, with significant differences in the levels of hTERT mRNA expression: 1, normal and reactive hyperplastic oral epithelium, and 2, atypical hyperplasia, intraepithelial carcinomas and squamous cell carcinomas.

CONCLUSION

These data suggest that hTERT gene re-expression represents an early event in the multistep process of oral carcinogenesis, already detectable at the stage of precancerous oral epithelial changes. Nevertheless, other genetic aberrations appear to be necessary for progression of oral epithelial abnormalities towards invasive squamous cell carcinoma.

摘要

目的

端粒酶催化亚基(hTERT)mRNA的检测已被用作评估端粒酶活性的替代标志物。端粒酶是一种与细胞永生化和转化相关的关键酶,在口腔癌发生的多步骤过程中,其重新激活的确切作用和时间仍不清楚。本研究旨在验证以下假设:(i)正常口腔黏膜、不同等级的口腔上皮异常和口腔鳞状细胞癌之间,hTERT mRNA表达水平存在定量而非定性差异;(ii)hTERT基因重新表达是口腔癌发生过程中的一个重要事件,可能是早期事件。

方法与结果

使用市售的LightCycler Telo TAGGG hTERT定量试剂盒,分析了45个根据卢布尔雅那分类法分类的代表口腔癌发生不同形态阶段的冷冻口腔上皮组织,以及37例口腔鳞状细胞癌中hTERT mRNA的相对含量。在正常或反应性增生的口腔上皮中未检测到hTERT mRNA,但在43%的非典型增生(癌前病变)、60%的上皮内癌和68%的口腔鳞状细胞癌中检测到。统计分析显示口腔上皮变化分为两组,hTERT mRNA表达水平存在显著差异:1. 正常和反应性增生的口腔上皮;2. 非典型增生、上皮内癌和鳞状细胞癌。

结论

这些数据表明,hTERT基因重新表达是口腔癌发生多步骤过程中的早期事件,在癌前口腔上皮变化阶段即可检测到。然而,口腔上皮异常向浸润性鳞状细胞癌进展似乎还需要其他基因异常。

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