Effective inhibition of hTERT expression by RNA interference on the radiosensitivity of human laryngeal cancer Hep-2 cell line.
- Author:
Hui-bing QIU
1
;
Yun-feng ZHOU
;
Fu-xiang ZHOU
;
Cong-hua XIE
;
Zhi-guo LUO
;
Hai-jun YU
;
Shi-quan LIU
Author Information
- Publication Type:Journal Article
- MeSH: Carcinoma, Squamous Cell; enzymology; genetics; pathology; Cell Line, Tumor; Cell Survival; genetics; radiation effects; Cobalt Radioisotopes; Enzyme-Linked Immunosorbent Assay; Gamma Rays; Humans; Laryngeal Neoplasms; enzymology; genetics; pathology; Plasmids; RNA Interference; RNA, Messenger; biosynthesis; genetics; RNA, Small Interfering; genetics; Recombinant Proteins; biosynthesis; Telomerase; genetics; metabolism; Transfection
- From: Chinese Journal of Oncology 2007;29(1):9-13
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo construct an eukaryotic expression vector of human telomerase reverse transcriptase (hTERT) gene specific shRNA, and investigate the effect of pshRNA-hTERT combined with gamma-irradiation on cell survival and telomerase activity.
METHODSAccording to the coding sequence of hTERT mRNA, the target of RNAi was designed, and recombinant expression plasmid pshRNA-hTERT was constructed. The vector was transfected into Hep-2 cells. The radiosensitivity of Hep-2 cells was determined by clonogenic assay. Telomeric repeat amplification protocol (TRAP-PCR-ELISA) was used to observe the telomerase activity in each group. Results Recombinant expression vector pshRNA-hTERT was successfully transfected into Hep-2 cells. The hTERT expression inhibition rate reached 60. 8%. pshRNA-hTERT not only inhibited telomerase activity of Hep-2, but also inhibited the raise of telomerase activity induced by gamma-irradiation. Exposure of Hep-2 cells to pshRNA-hTERT for 24 hrs before irradiation resulted in a decrease in mean surviving fraction of Hep-2 cells compared with cells of group with irradiation alone (67. 7% vs 85. 7%, P <0. 05) .
CONCLUSIONRNAi showed a significant inhibitory effect to the expression of hTERT. The results indicate that pshRNA-hTERT can effectively inhibit telomerase activity of Hep-2 cells treated or untreated with 2 Gy gamma-irradiation and significantly enhance the radiosensitivity of Hep-2 cells in vitro. The role of radiosensitization of pshRNA-hTERT may be related with the inhibition of telomerase activity.