Silencing of COX-2 in nasopharyngeal carcinoma cells with a shRNAmir lentivirus vector.
- Author:
Gang LI
1
;
Xiang-Ping LI
;
Li JIANG
;
Juan LU
;
Xiong LIU
;
Shun-Jin CHEN
Author Information
- Publication Type:Journal Article
- MeSH: Cell Line, Tumor; Cyclooxygenase 2; genetics; Genetic Vectors; genetics; Humans; Lentivirus; genetics; metabolism; MicroRNAs; genetics; Nasopharyngeal Neoplasms; genetics; metabolism; pathology; RNA Interference; RNA, Small Interfering; genetics; Transfection
- From: Journal of Southern Medical University 2009;29(6):1111-1114
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo construct a miR-155-based lentivirus vector to induce cyclooxygenase-2 gene silencing in nasopharyngeal carcinoma (NPC) cells by expressing anti-COX-2 shRNAmir.
METHODSmiR-155-based anti-COX-2 shRNAmir template was synthesized and inserted into pLVTHM plasmid. The recombinant pLVTHM/shRNAmir was transfected into 293FT cells for packaging the lentivirus vector. After infection with the lentivirus vector, the GFP-positive cells were screened by flow cytometry, and COX-2 mRNA level was detected by RT-PCR.
RESULTSRestriction digestion and DNA sequencing confirmed successful construction of the anti-COX-2 vector pLVTHM/shRNAmir. A subline of C666-1 cells was established after infection with the lentivirus vector, and the COX-2 expression in the cells was stably silenced.
CONCLUSIONThe shRNAmir lentivirus vector constructed may serve as an effective COX-2 inhibitor, which may facilitate future studies of gene therapy of NPC.