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Provedor de dados:  Genet. Mol. Biol.
País:  Brazil
Título:  RNAi-mediated silencing of the Bmi-1 gene causes growth inhibition and enhances doxorubicin-induced apoptosis in MCF-7 cells
Autores:  Wu,Xiang-mei
Liu,Xing
Bu,You-quan
Sengupta,Joyeeta
Cui,Hong-juan
Yi,Fa-ping
Liu,Tao
Yuan,Chen-fu
Shi,Yan-yan
Song,Fang-zhou
Data:  2009-01-01
Ano:  2009
Palavras-chave:  RNA interference
Bmi-1
Retrovirus vector
Doxorubicin
Breast cancer
Resumo:  The oncogene Bmi-1 is a member of the Polycomb group gene family. Its expression is found to be greatly increased in a number of malignant tumors including breast cancer. This could suggest Bmi-1 as a potent therapeutic target. In this study, RNAi was introduced to down-regulate the expression of Bmi-1 in a highly malignant breast adenocarcinoma cell line, MCF-7. A thorough study of the biological behavior and chemosensitivity changes of the MCF-7 cells was carried out in context to the therapeutic potential of Bmi-1. The results obtained indicated that siRNA targeting of Bmi-1 could lead to an efficient and specific inhibition of endogenous Bmi-1 activity. The mRNA and protein expression of Bmi-1 were determined by RT-PCR and Western blot, respectively. Furthermore, silencing of Bmi-1 resulted in a drastic inhibition of the growth of MCF-7 cells as well as G1/S phase transition. The number of target cells was found to increase in phase G0/G1 and decrease in the S phase, but no increase in the basal level of apoptosis was noticed. On the other hand, a reduction in the expression of cyclin D1 and an increase in the expression of p21 were also noticed. Silencing of Bmi-1 made the MCF-7 cells more sensitive to the chemotherapeutic agent doxorubicin and induced a significantly higher percentage of apoptotic cells. Here, we report on a study regarding the RNAi-mediated silencing of the Bmi-1 gene in breast cancer.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572009000400004
Editor:  Sociedade Brasileira de Genética
Relação:  10.1590/S1415-47572009005000092
Formato:  text/html
Fonte:  Genetics and Molecular Biology v.32 n.4 2009
Direitos:  info:eu-repo/semantics/openAccess
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