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Oncotarget ; 7(24): 35894-35916, 2016 Jun 14.
Article in English | MEDLINE | ID: mdl-27145285

ABSTRACT

AIM: To investigate the use of thermosensitive magnetoliposomes (TMs) loaded with magnetic iron oxide (Fe3O4) and the anti-cancer stem cell marker CD90 (CD90@TMs) to target and kill CD90+ liver cancer stem cells (LCSCs). METHODS: The hepatocellular carcinoma cell line Huh7 was used to separate CD90+ LCSCs by magnetic-activated cell sorting. CD90@TMs was characterized and their ability to target CD90+ LCSCs was determined. Experiments were used to investigate whether CD90@TMs combined with magnetic hyperthermia could effectively eliminate CD90+ LCSCs. RESULTS: The present study demonstrated that CD90+ LCSCs with stem cells properties were successfully isolated. We also successfully prepared CD90@TMs that was almost spherical and uniform with an average diameter of 130±4.6 nm and determined that magnetic iron oxide could be incorporated and retained a superparamagnetic response. CD90@TMs showed good targeting and increased inhibition of CD90+ LCSCs in vitro and in vivo compared to TMs. CONCLUSIONS: CD90@TMs can be used for controlled and targeted delivery of anticancer drugs, which may offer a promising alternative for HCC therapy.


Subject(s)
Antibodies/immunology , Carcinoma, Hepatocellular/immunology , Liver Neoplasms/immunology , Neoplastic Stem Cells/immunology , Thy-1 Antigens/immunology , Animals , Antibodies/pharmacology , Apoptosis/drug effects , Apoptosis/immunology , Carcinoma, Hepatocellular/drug therapy , Carcinoma, Hepatocellular/metabolism , Cell Line , Cell Line, Tumor , Cell Proliferation/drug effects , Humans , Immunomagnetic Separation/methods , Liver Neoplasms/drug therapy , Liver Neoplasms/metabolism , Mice, Inbred NOD , Mice, SCID , Neoplastic Stem Cells/drug effects , Neoplastic Stem Cells/metabolism , Temperature , Thy-1 Antigens/metabolism , Xenograft Model Antitumor Assays/methods
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