Apoptosis of glioma cell line U251 induced by small interfering RNA targeting survivin.
- Author:
Ru-xiang XU
1
;
Yan-yang TU
;
Xiao-dan JIANG
;
Jiang-nan FENG
;
Jun HUANG
Author Information
- Publication Type:Journal Article
- MeSH: Apoptosis; physiology; Brain Neoplasms; metabolism; pathology; Cell Division; Cell Line, Tumor; Genetic Therapy; Glioma; metabolism; pathology; Humans; Inhibitor of Apoptosis Proteins; Microtubule-Associated Proteins; biosynthesis; genetics; Neoplasm Proteins; biosynthesis; genetics; RNA, Antisense; genetics; RNA, Small Interfering; Transfection
- From: Journal of Southern Medical University 2006;26(4):398-401
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo construct recombinant expression vectors of small interfering RNA (siRNA) targeting survivin and investigate apoptosis of glioma cell line U251 mediated by the survivin-targeting siRNA.
METHODSAccording to the sequence of the coding region of survivin gene, two strings of 19 nucleotides of inverted sequence flanking the loop sequence of two complementary 9-base oligonucleotides were designed and synthesized to form hairpin construct as the DNA templates for the target siRNA. The siRNA templates were cloned into siRNA expression vector pGenesil-1, and the resulted vector pGenesil-1/survivin was transfected into U251 cells using Metafectene following the standard protocols. Real-time PCR and Western blotting were performed to evaluate survivin gene silencing induced by siRNA transfection at the RNA and protein levels, respectively. Flow cytometry analysis with Annexin-V/PI double staining was used to determine the cell apoptosis.
RESULTSReal-time RT-PCR and Western blotting revealed significantly lowered survivin expression at both RNA and protein levels in transfected U251 cells, which exhibited a significantly higher apoptosis rate after transfection as shown by flow cytometry analysis.
CONCLUSIONRNA interference mediated by the siRNA expression vector pGenesi-l/survivin can significantly reduce survivin expression and induce remarkable apoptosis in U251 cells.