The inhibitory effect of antisense adenovirus vector of telomerase on telomerase activity in breast cancer cells MCF -7
Tanjun Tong
Abstract
Tanjun Tong
Abstract
Objective To inhibit telomerase activity in breast cancer cells MCF 7 by antisense ribonucleotide technique. Methods Recombinant adenovirus was chosen as gene delivery vector to transfer and express the antisense RNA component of telomerase in tumor cells. The recombinant adenovirus of anti telomerase RNA was obtained through gene recombination and co transfection with lipofectin. The integrated potential of antisense virus was certified by Southern blot and the telomerase activity of MCF 7 was analysed by TRAP silver staining. Results The MCF 7 cell line is a typical model for malignant breast cancer. In this study, the telomerase activity of MCF 7 was significantly inhibited after antisense virus infection when compared with the control cell lines. Conclusion The introduction of antisense cDNA of telomerase RNA can significantly inhibit the activity of telomerase in MCF 7 cells.
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Objective To inhibit telomerase activity in breast cancer cells MCF 7 by antisense ribonucleotide technique. Methods Recombinant adenovirus was chosen as gene delivery vector to transfer and express the antisense RNA component of telomerase in tumor cells. The recombinant adenovirus of anti telomerase RNA was obtained through gene recombination and co transfection with lipofectin. The integrated potential of antisense virus was certified by Southern blot and the telomerase activity of MCF 7 was analysed by TRAP silver staining. Results The MCF 7 cell line is a typical model for malignant breast cancer. In this study, the telomerase activity of MCF 7 was significantly inhibited after antisense virus infection when compared with the control cell lines. Conclusion The introduction of antisense cDNA of telomerase RNA can significantly inhibit the activity of telomerase in MCF 7 cells.
Key concepts: Telomerase, MCF-7, Telomerase reverse transcriptase, Molecular biology, Antisense RNA, Transfection, Biology, Cell culture