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Effective elimination of liver cancer stem-like cells by CD90 antibody targeted thermosensitive magnetoliposomes
AIM: To investigate the use of thermosensitive magnetoliposomes (TMs) loaded with magnetic iron oxide (Fe(3)O(4)) 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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094971/ https://www.ncbi.nlm.nih.gov/pubmed/27145285 http://dx.doi.org/10.18632/oncotarget.9116 |
Sumario: | AIM: To investigate the use of thermosensitive magnetoliposomes (TMs) loaded with magnetic iron oxide (Fe(3)O(4)) 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. CONCLUSION: CD90@TMs can be used for controlled and targeted delivery of anticancer drugs, which may offer a promising alternative for HCC therapy. |
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