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In vitro effect of hyperthermic Ag and Au Fe3O4 nanoparticles in cancer cells.
Katifelis, Hector; Lyberopoulou, Anna; Vityuk, Nadiia; Grammatikaki, Matina; Pylypchuk, Ievgen; Lazaris, Foivos; Storozhuk, Liudmyla; Kouloulias, Vassilios; Gazouli, Maria.
Afiliação
  • Katifelis H; Laboratory of Biology, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
J BUON ; 25(2): 1212-1218, 2020.
Article em En | MEDLINE | ID: mdl-32521928
ABSTRACT

PURPOSE:

To investigate the anti-cancer efficacy of hyperthermic Ag and Au Fe3O4 core nanoparticles via cytotoxicity study (MTT assay) and the underlying molecular mechanism of action (changes in gene expression via quantitive real time PCR (qRT-PCR).

METHODS:

HEK293, HCT116, 4T1 and HUH7 human cell lines and 4T1 musculus mammary gland cell line were incubated with Fe3O4 core Ag(Au) shell nanoparticles (NPs) prior to a hyperthermia session. MTT assay was performed to estimate the cytotoxic effects of these NPs. RNA extraction and cDNA synthesis followed so as to quantify mRNA fold change of hsp-70, p53, bcl-2 and casp-3 via qRT-PCR.

RESULTS:

Fe3O4 core Au shell (concentrations of 400 and 600µg/mL) produced the greatest reduction of viability on HCT116 and 4T1 cells while Fe3O4 core Ag shell (200, 400 and 600µg/mL) reduce viability on HUH7 cells. Hsp-70, p53 and casp-3 were up-regulated while bcl-2 was downregulated in most cases.

CONCLUSIONS:

Fe3O4 core Ag (Au) shell induced apoptosis on cancer cells (HCT116 and HUH7) via the p53/bcl-2/casp-3 pathway. 4T1 cells also underwent apoptosis via a p53-independent pathway.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prata / Nanopartículas Metálicas / Ouro / Hipertermia Induzida / Neoplasias Limite: Humans Idioma: En Revista: J BUON Assunto da revista: NEOPLASIAS Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Grécia
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Prata / Nanopartículas Metálicas / Ouro / Hipertermia Induzida / Neoplasias Limite: Humans Idioma: En Revista: J BUON Assunto da revista: NEOPLASIAS Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Grécia