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DN-hTERT对骨肉瘤细胞生长和端粒酶活性的抑制作用

Inhibition of cell growth and telomerase activity in osteosarcoma cells by DN-hTERT.

作者信息

Xu Tao, Rao Yaojian, Zhu Wentao, Guo Fengjin

机构信息

Department of Rehabilitation Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2006;26(5):601-3. doi: 10.1007/s11596-006-0532-5.

Abstract

In order to study the effects of dominant negative human telomerase reverse transcriptase (DN-hTERT) on cell growth and telomerase activity in osteosarcoma cell line MG63, MG63 cells were transfected with DN-hTERT-IRES2-EGFP9 (DN) or IRES2-EGF (I, blank vector) with lipofectamine 2000. The stably transfected cells were selected with G-418. Cell growth properties were examined under a fluorescence microscope. The hTERT mRNA expression was detected by reverse transcription-polymerase chain reaction (RT-PCR). Telomerase activities were measured by TRAP-ELISE. The tumorigenicity was studied with tumor xenografts by subcutaneous injection of cancer cells into nude mice. The results showed that cell growth was suppressed in MG63 cells transfected with DN-hTERT. The hTERT mRNA was increased in N-hTERT transfected-MG63 cells (MG63/DN). The telomerase activity was 2.45-0.11 in MG63/DN cells, while 3.40+/-0.12 in the cells transfected with blank vector (MG63/I), (P<0.05); DN-hTERT-expressing clones did not form tumors in 2 weeks, but the ratio of tumorigenesis was 30 % in nude mice bearing MG63/I (P<0.01). It was concluded that DN-hTERT could specifically inhibit the cell growth and telomerase activity in MG63 cells.

摘要

为研究显性负性人端粒酶逆转录酶(DN-hTERT)对骨肉瘤细胞系MG63细胞生长及端粒酶活性的影响,采用脂质体2000将DN-hTERT-IRES2-EGFP9(DN)或IRES2-EGF(I,空载体)转染至MG63细胞。用G-418筛选稳定转染的细胞。在荧光显微镜下检测细胞生长特性。通过逆转录-聚合酶链反应(RT-PCR)检测hTERT mRNA表达。采用端粒重复序列扩增酶联免疫吸附测定(TRAP-ELISE)法检测端粒酶活性。通过将癌细胞皮下注射到裸鼠体内形成肿瘤异种移植来研究致瘤性。结果显示,转染DN-hTERT的MG63细胞生长受到抑制。在转染N-hTERT的MG63细胞(MG63/DN)中hTERT mRNA增加。MG63/DN细胞中端粒酶活性为2.45±0.11,而转染空载体的细胞(MG63/I)中端粒酶活性为3.40±0.12,(P<0.05);表达DN-hTERT的克隆在2周内未形成肿瘤,但接种MG63/I的裸鼠致瘤率为30%,(P<0.01)。结论:DN-hTERT可特异性抑制MG63细胞的生长及端粒酶活性。

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