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Authors Xie WS, Gao Q, Wang D, Wang W, Yuan J, Guo Z, Yan H, Wang X, Sun X, Zhao L
Received 7 August 2017
Accepted for publication 31 August 2017
Published 11 October 2017 Volume 2017:12 Pages 7351—7363
DOI https://doi.org/10.2147/IJN.S148520
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Alicia Fernandez-Fernandez
Peer reviewer comments 3
Editor who approved publication: Professor Dongwoo Khang
Purpose: With the wide recognition of oncostatic effect of melatonin, the current
study proposes a potential breast cancer target multimodality treatment based
on melatonin-loaded magnetic nanocomposite particles (Melatonin-MNPs).
Methods: Melatonin-MNPs were fabricated by the single
emulsion solvent extraction/evaporation method.
Results: Based on the facilitated transport of melatonin
by the GLUT overexpressed on the cell membrane, such Melatonin-MNPs can be more
favorably uptaken by MCF-7 cells compared with the melatonin-free nanocomposite
particles, which indicates the cancer targeting ability of melatonin molecule.
Inductive heating can be generated by exposure to the Melatonin-MNPs
internalized within cancer cells under alternative magnetic field, so as to
achieve the “inside-out” magnetic nano-thermotherapy. In addition to
demonstrating the superior cytotoxic effect of such nano-thermotherapy over the
conventional exogenous heating by metal bath, more importantly, the sustainable
release of melatonin from the Melatonin-MNPs can be greatly promoted upon
responsive to the magnetic heating. The multimodality treatment based on
Melatonin-MNPs can lead to more significant decrease in cell viability than any
single treatment, suggesting the potentiated effect of melatonin on the
cytotoxic response to nano-thermotherapy.
Conclusion: This study is the first to fabricate the
precisely engineered melatonin-loaded multifunctional nanocomposite particles
and demonstrate the potential in breast cancer target multimodality treatment.
Keywords: melatonin,
magnetic nano-thermotherapy, multifunctional nanoparticles, breast cancer,
cancer multimodality treatment, cancer target