Effect of RNAi-mediated gene silencing of Livin on apoptosis of human breast cancer cell line ZR-75-30 | |
Alternative Title | Effect of RNAi-mediated gene silencing of Livin on apoptosis of human breast cancer cell line ZR-75-30 |
Liang Chunyan; Ma Ping | |
2008 | |
Source Publication | CHINESE JOURNAL OF CANCER RESEARCH
![]() |
ISSN | 1000-9604 |
Volume | 20Issue:2Pages:100-104 |
Abstract | Objective: To explore the effects of Livin gene knock down using sequence-specific siRNA on apoptosis of human breast cancer cell ZR-75-30. Methods: Chemically synthesized double stranded RNA( dsRNA) targeting Livin was transfected into human breast cancer cell ZR-75-30 with lipofectamine(TM)2000. The transfection efficiency was observed under a fluorescence confocal microscope. Expression of Livin at both mRNA and protein levels were detected by reverse transcription-polymerase chain reaction(RT-PCR) and immunohistochemical analysis. The effects on apoptosis of ZR-75-30 cells were assessed by FCAS. Results: The Livin siRNA can effectively and specifically inhibited the expression of Livin gene in ZR-75-30. The inhibition rate was 53.66% at mRNA level and 58.32% at protein level. After 24h, (8.36 +/- 0.20)% cells transfected with siRNA were induced to apoptosis. Conclusion: Chemically synthesized short Livin-siRNA can effectively inhibit Livin over expression and remarkably induce apoptosis in human breast cancer cell line ZR-75-30. Livin RNAi has a potential value in gene therapy of breast cancer. |
Other Abstract | Objective:To explore the effects of Livin gene knock down using sequence-specific siRNA on apoptosis of human breast cancer cell ZR-75-30.Methods:Chemically synthesized double stranded RNA(dsRNA)targeting Livin was transfected into human breast cancer cell ZR-75-30 with lipofectamine~(TM)2000.The transfection efficiency was observed under a fluorescence confocal microscope.Expression of Livin at both mRNA and protein levels were detected by reverse transcription-polymerase chain reaction(RT-PCR)and immunohistochemical:analysis.The effects on apoptosis of ZR-75-30 cells were assessed by FCAS.Results:The Livin siRNA can effectively and specifically inhibited the expression of Livin gene in ZR-75-30.The inhibition rate was 53.66% at mRNA level and 58.32% at protein level.After 24h,(8.36±0.20)%cells transfected with siRNA were induced to apoptosis.Conclusion:Chemically synthesized short Livin-siRNA can effectively inhibit Livin over expression and remarkably induce apoptosis in human breast cancer cell line ZR-75-30.Livin RNAi has a potential value in gene therapy of breast cancer. |
Keyword | PROTEIN FAMILY MESSENGER-RNA INHIBITOR INTERFERENCE SURVIVIN SIRNA EXPRESSION MEMBER DEATH Livin breast cancer RNA interference apoptosis |
Indexed By | CSCD |
Language | 英语 |
CSCD ID | CSCD:3299649 |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://ir.imr.ac.cn/handle/321006/154105 |
Collection | 中国科学院金属研究所 |
Affiliation | 中国科学院金属研究所 |
Recommended Citation GB/T 7714 | Liang Chunyan,Ma Ping. Effect of RNAi-mediated gene silencing of Livin on apoptosis of human breast cancer cell line ZR-75-30[J]. CHINESE JOURNAL OF CANCER RESEARCH,2008,20(2):100-104. |
APA | Liang Chunyan,&Ma Ping.(2008).Effect of RNAi-mediated gene silencing of Livin on apoptosis of human breast cancer cell line ZR-75-30.CHINESE JOURNAL OF CANCER RESEARCH,20(2),100-104. |
MLA | Liang Chunyan,et al."Effect of RNAi-mediated gene silencing of Livin on apoptosis of human breast cancer cell line ZR-75-30".CHINESE JOURNAL OF CANCER RESEARCH 20.2(2008):100-104. |
Files in This Item: | There are no files associated with this item. |
Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.
Edit Comment