Antisense hTERT inhibits gene expression and functional activity of telomerase in leukemia cell lines.
- Author:
Lai-bao SUN
1
;
Cheng-rong LI
;
Jian-ming WEN
;
Guo-bing WANG
;
Meng ZHANG
;
Jun YANG
;
Ruo-xin LI
Author Information
- Publication Type:Journal Article
- MeSH: Apoptosis; Cell Cycle; DNA-Binding Proteins; biosynthesis; genetics; Down-Regulation; Gene Expression Regulation, Neoplastic; Genetic Vectors; HL-60 Cells; HeLa Cells; Humans; K562 Cells; RNA, Antisense; genetics; RNA, Messenger; biosynthesis; genetics; Recombinant Proteins; biosynthesis; genetics; Telomerase; biosynthesis; genetics; metabolism; Transfection
- From: Chinese Journal of Pathology 2004;33(5):454-457
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo explore the inhibitory effects of gene expression and functional activity of telomerase in leukemia cell lines by in vitro antisense hTERT treatment.
METHODSAn antisense hTERT eukaryotic expression vector was constructed by using gene recombination technique, targeting the 5' end mRNA sequence of the telomerase catalytic subunit. The vector expression in leukemia cell lines (HL60 and K562) was achieved by transfection using the SuperFect transfection reagent (Qiagen). After transfection, ectopic expression of the telomerase catalytic subunit was analyzed by quantitative fluorescence real-time RT-PCR, and cellular apoptosis and cell cycle parameters were evaluated by flow cytometry respectively.
RESULTSAn antisense pcDNA-hTERT eukaryotic expression vector was successfully constructed. Leukemia cell lines transfected with antisense hTERT constructed displayed a significant inhibition of gene expression of telomerase and its activity in vitro, as compared with the result of the control groups (without transfection and vector control).
CONCLUSIONIn-vitro antisense hTERT expression may down-regulate the gene expression and biological activity of telomerase in leukemia cells, suggesting a possibility of gene therapy against human malignancy through the telomerase-targeted molecular mechanism.