Your browser doesn't support javascript.
loading
Therapeutic mechanism of treating SMMC-7721 liver cancer cells with magnetic fluid hyperthermia using Fe2O3 nanoparticles.
Yan, S Y; Chen, M M; Fan, J G; Wang, Y Q; Du, Y Q; Hu, Y; Xu, L M.
Afiliação
  • Yan SY; Department of Gastroenterology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Chen MM; Department of Gastroenterology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Fan JG; Department of Gastroenterology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Wang YQ; Department of Gastroenterology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Du YQ; Department of Pathology, Cancer Hospital, Fudan University, Shanghai, China.
  • Hu Y; Department of Gastroenterology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Xu LM; Department of Gastroenterology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
Braz J Med Biol Res ; 47(11): 947-59, 2014 Nov.
Article em En | MEDLINE | ID: mdl-25296356
This study aimed to investigate the therapeutic mechanism of treating SMMC-7721 liver cancer cells with magnetic fluid hyperthermia (MFH) using Fe2O3 nanoparticles. Hepatocarcinoma SMMC-7721 cells cultured in vitro were treated with ferrofluid containing Fe2O3 nanoparticles and irradiated with an alternating radio frequency magnetic field. The influence of the treatment on the cells was examined by inverted microscopy, MTT and flow cytometry. To study the therapeutic mechanism of the Fe2O3 MFH, Hsp70, Bax, Bcl-2 and p53 were detected by immunocytochemistry and reverse transcription polymerase chain reaction (RT-PCR). It was shown that Fe2O3 MFH could cause cellular necrosis, induce cellular apoptosis, and significantly inhibit cellular growth, all of which appeared to be dependent on the concentration of the Fe2O3nanoparticles. Immunocytochemistry results showed that MFH could induce high expression of Hsp70 and Bax, decrease the expression of mutant p53, and had little effect on Bcl-2. RT-PCR indicated that Hsp70 expression was high in the early stage of MFH (<24 h) and became low or absent after 24 h of MFH treatment. It can be concluded that Fe2O3MFH significantly inhibited the proliferation of in vitro cultured liver cancer cells (SMMC-7721), induced cell apoptosis and arrested the cell cycle at the G2/M phase. Fe2O3 MFH can induce high Hsp70 expression at an early stage, enhance the expression of Bax, and decrease the expression of mutant p53, which promotes the apoptosis of tumor cells.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Compostos Férricos / Carcinoma Hepatocelular / Nanopartículas / Magnetoterapia / Hipertermia Induzida / Neoplasias Hepáticas Limite: Humans Idioma: En Revista: Braz J Med Biol Res Ano de publicação: 2014 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Compostos Férricos / Carcinoma Hepatocelular / Nanopartículas / Magnetoterapia / Hipertermia Induzida / Neoplasias Hepáticas Limite: Humans Idioma: En Revista: Braz J Med Biol Res Ano de publicação: 2014 Tipo de documento: Article País de afiliação: China