Knockdown of survivin expression by small interfering RNA suppresses proliferation of two human cancer cell lines.
- Author:
Hai-Tao GUAN
1
;
Xing-Huan XUE
;
Xi-Jing WANG
;
Ang LI
;
Zhao-Yin QIN
Author Information
- Publication Type:Journal Article
- MeSH: Base Sequence; Breast Neoplasms; pathology; therapy; Cell Line, Tumor; Cell Proliferation; Female; Gene Expression; Humans; Inhibitor of Apoptosis Proteins; Microtubule-Associated Proteins; antagonists & inhibitors; genetics; metabolism; Pancreatic Neoplasms; pathology; therapy; Plasmids; genetics; RNA, Messenger; genetics; metabolism; RNA, Neoplasm; genetics; metabolism; RNA, Small Interfering; genetics; therapeutic use; Transfection
- From: Chinese Medical Sciences Journal 2006;21(2):115-119
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo construct an expression vector of small interfering RNA (siRNA) against survivin and observe its effects on survivin expression and proliferation of human pancreatic cancer cell line PC-2 and breast cancer cell line MCF-7.
METHODSConstructed an expression vector of siRNA against survivin and transfected it into PC-2 and MCF-7 cells using lipofectamine 2000. The expression of survivin was detected by semi-quantitive RT-PCR and immunohistochemistry, and its effects on proliferation of PC-2 and MCF-7 cells were detected by MTT assay.
RESULTSThe introduction of sequence-specific siRNA could efficiently suppress survivin expression at both mRNA and protein levels in the two cancer cell lines. In PC-2 cells, the expression inhibition rates were 81.25% at mRNA level and 74.24% at protein level. In MCF-7 cells, the expression inhibition rates were 64.91% at mRNA level and 79.72% at protein level. The proliferation of PC-2 and MCF-7 cells was also suppressed, and 24 and 48 hours after the cells were reseeded, the proliferation inhibition rates of PC-2 cells were 28.00% and 33.38%, and that of MCF-7 cells were 31.58% and 33.02%, respectively.
CONCLUSIONSThe expression vector of siRNA against survivin can block survivin expression in PC-2 and MCF-7 cells efficiently and specifically. Down regulation of survivin expression can suppress proliferation of PC-2 and MCF-7 cells. Survivin RNAi may have potential value in gene therapy of human cancers.