4.3 Article

Effective elimination of liver cancer stem-like cells by CD90 antibody targeted thermosensitive magnetoliposomes

Journal

ONCOTARGET
Volume 7, Issue 24, Pages 35894-35916

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.9116

Keywords

LCSCs; CD90; TMs; targeting therapy; hyperthermia therapy

Funding

  1. National Key Basic Research Program of China (973 Program) [2013CB933904, 2011CB933500]
  2. National Natural Science Foundation of China [81271635, 81301270, 81201131]
  3. Natural Science Foundation of Jiangsu Province [BK2012335]
  4. Fundamental Research Funds for the Central Universities
  5. Regular University Graduate Student Scientific Research Innovation Projects of Jiangsu Province [KYLX_0204]
  6. Scientific Research Foundation of Graduate School of Southeast University
  7. Southeast University Excellent Doctor Degree Thesis Training Fund [YBJJ1459]

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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. 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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