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人原位口腔癌发生过程中,hTERT的高表达与发育异常细胞转化相关。

Elevated expression of hTERT is associated with dysplastic cell transformation during human oral carcinogenesis in situ.

作者信息

Kim H R, Christensen R, Park N H, Sapp P, Kang M K, Park N H

机构信息

Dental Research Institute, University of California, Los Angeles, 90095, USA.

出版信息

Clin Cancer Res. 2001 Oct;7(10):3079-86.

Abstract

PURPOSE

Telomerase is a ribonucleoprotein complex composed of the catalytic protein subunit (human telomerase reverse transcriptase or hTERT) and the RNA template. This enzyme activity is a necessary and rate-limiting step of cellular immortalization and could provide a unique marker of aberrant cells, which may selectively be targeted. The current study was undertaken to quantitatively determine the degree of telomerase activation during multistage oral carcinogenesis using paraffin-embedded tissue samples.

EXPERIMENTAL DESIGN

hTERT expression level was quantitatively compared between normal and cancerous oral tissues by real-time reverse-transcription-PCR (RT-PCR). Also, the presence of hTERT transcript in individual cells was surveyed in the biopsy specimens with varying degrees of histopathology by in situ RT-PCR.

RESULTS

Low level of hTERT amplification was detected by real-time RT-PCR in most (11/13) normal human oral mucosa. hTERT expression was also detected in the majority (11/12) of squamous cell carcinoma tissues, and the level was significantly (P < 0.05) elevated, on the average, by a factor >6.9. By in situ RT-PCR, hTERT expression was not noted in normal epithelium (0/10) nor in mild dysplasia (0/7) but was detected in moderate dysplasia (4/5) and in those tissues with a higher grade of histopathology: severe dysplasia (3/3) and invasive carcinoma (4/4).

CONCLUSIONS

These results indicate that enhanced expression of telomerase activity occurs early during human oral carcinogenesis and support the critical role of telomerase in the development of human oral cancer.

摘要

目的

端粒酶是一种核糖核蛋白复合体,由催化蛋白亚基(人类端粒酶逆转录酶或hTERT)和RNA模板组成。这种酶活性是细胞永生化的必要且限速步骤,并且可以提供异常细胞的独特标志物,这些异常细胞可能成为选择性靶向的目标。本研究旨在使用石蜡包埋组织样本定量测定多阶段口腔癌发生过程中端粒酶激活的程度。

实验设计

通过实时逆转录PCR(RT-PCR)定量比较正常口腔组织和癌性口腔组织之间的hTERT表达水平。此外,通过原位RT-PCR在具有不同程度组织病理学的活检标本中检测单个细胞中hTERT转录本的存在情况。

结果

通过实时RT-PCR在大多数(11/13)正常人口腔黏膜中检测到低水平的hTERT扩增。在大多数(11/12)鳞状细胞癌组织中也检测到hTERT表达,并且平均水平显著(P < 0.05)升高,升高因子>6.9。通过原位RT-PCR,在正常上皮(0/10)和轻度发育异常(0/7)中未观察到hTERT表达,但在中度发育异常(4/5)以及组织病理学分级更高的组织中检测到:重度发育异常(3/3)和浸润性癌(4/4)。

结论

这些结果表明端粒酶活性增强表达在人类口腔癌发生早期出现,并支持端粒酶在人类口腔癌发展中的关键作用。

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