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Provedor de dados:  BJMBR
País:  Brazil
Título:  Co-culture of apoptotic breast cancer cells with immature dendritic cells: a novel approach for DC-based vaccination in breast cancer
Autores:  Zheng,Jin
Liu,Qiang
Yang,Jiandong
Ren,Qinyou
Cao,Wei
Yang,Jingyue
Yu,Zhaocai
Yu,Fang
Wu,Yanlan
Shi,Hengjun
Liu,Wenchao
Data:  2012-06-01
Ano:  2012
Palavras-chave:  Breast cancer
Dendritic cells
Immunotherapy
Apoptosis
Doxorubicin
Resumo:  A dendritic cell (DC)-based vaccine strategy could reduce the risk of recurrence and improve the survival of breast cancer patients. However, while therapy-induced apoptosis of hepatocellular and colorectal carcinoma cells can enhance maturation and antigen presentation of DCs, whether this effect occurs in breast cancer is currently unknown. In the present study, we investigated the effect of doxorubicin (ADM)-induced apoptotic MCF-7 breast cancer cells on the activation of DCs. ADM-induced apoptotic MCF-7 cells could effectively induce immature DC (iDC) maturation. The mean fluorescence intensity (MFI) of DC maturity marker CD83 was 23.3 in the ADM-induced apoptotic MCF-7 cell group compared with 8.5 in the MCF-7 cell group. The MFI of DC co-stimulatory marker CD86 and HLA-DR were also increased after iDCs were treated with ADM-induced apoptotic MCF-7 cells. Furthermore, the proliferating autologous T-lymphocytes increased from 14.2 to 40.3% after incubated with DCs induced by apoptotic MCF-7 cells. The secretion of interferon-γ by these T-lymphocytes was also increased. In addition, cell-cell interaction between apoptotic MCF-7 cells and iDCs, but not soluble factors released by apoptotic MCF-7 cells, was crucial for the maturation of iDCs. These findings constitute a novel in vitro DC-based vaccine strategy for the treatment of breast cancer by ADM-induced apoptotic MCF-7 cells.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012000600006
Editor:  Associação Brasileira de Divulgação Científica
Relação:  10.1590/S0100-879X2012007500061
Formato:  text/html
Fonte:  Brazilian Journal of Medical and Biological Research v.45 n.6 2012
Direitos:  info:eu-repo/semantics/openAccess
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