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[p53基因对涎腺腺样囊性癌细胞端粒酶活性及增殖活性的抑制作用]

[Inhibitory effect of p53 gene on telomerase activity and proliferative activity in salivary adenoid cystic carcinoma cells].

作者信息

Yan Bing-zhi, Wang Jie, Zhang Bo, Dong Fu-sheng, Hou Lin, Wang Xu

机构信息

Department of Oral Pathology, School of Stomatology, Hebei Medical University, Shijiazhuang 050017, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2006 Jan;41(1):45-8.

Abstract

OBJECTIVE

To evaluate the inhibitory effect of p53 gene on salivary adenoid cystic carcinoma (SACC) cells.

METHODS

Adenoviral vector pDeltaE1-p53 was constructed and transfected into SACC-83 cells. The enhanced p53 expression was measured by reverse transcription polymerase chain reaction (RT-PCR), and the effects of transfected p53 on SACC-83 cells were analyzed by TRAP-PCR-ELISA, luciferase reporter, flow cytometry (FCM), soft agar assay and tumorigenicity test.

RESULTS

The expression of p53 gene in SACC-83 cells was increased after introduction of pDeltaE1-p53. The telomerase activity and the transcriptional activity of hTERT promoter were inhibited. The cells cycles of transfected SACC-83 were arrested in G(1) phase and the rate of colony-formation was decreased, and similarly the tumorigenicity in nude mice was also decreased.

CONCLUSIONS

The introduction of wild-type p53 by adenoviral vector could suppress the telomerase activity and malignant phenotypes of salivary adenoid cystic carcinoma cells.

摘要

目的

评估p53基因对涎腺腺样囊性癌(SACC)细胞的抑制作用。

方法

构建腺病毒载体pDeltaE1-p53并转染至SACC-83细胞。通过逆转录聚合酶链反应(RT-PCR)检测p53表达增强情况,采用TRAP-PCR-ELISA、荧光素酶报告基因、流式细胞术(FCM)、软琼脂试验及致瘤性试验分析转染的p53对SACC-83细胞的影响。

结果

导入pDeltaE1-p53后,SACC-83细胞中p53基因表达增加。端粒酶活性及hTERT启动子的转录活性受到抑制。转染的SACC-83细胞周期阻滞于G(1)期,集落形成率降低,同样在裸鼠中的致瘤性也降低。

结论

通过腺病毒载体导入野生型p53可抑制涎腺腺样囊性癌细胞的端粒酶活性及恶性表型。

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