Volume 8, Issue 2 , Pages 136-146, February 2012
Gadolinium metallofullerenol nanoparticles inhibit cancer metastasis through matrix metalloproteinase inhibition: imprisoning instead of poisoning cancer cells
Abstract
The purpose of this work is to study the antimetastasis activity of gadolinium metallofullerenol nanoparticles (f-NPs) in malignant and invasive human breast cancer models. We demonstrated that f-NPs inhibited the production of matrix metalloproteinase (MMP) enzymes and further interfered with the invasiveness of cancer cells in tissue culture condition. In the tissue invasion animal model, the invasive primary tumor treated with f-NPs showed significantly less metastasis to the ectopic site along with the decreased MMP expression. In the same animal model, we observed the formation of a fibrous cage that may serve as a physical barrier capable of cancer tissue encapsulation that cuts the communication between cancer- and tumor-associated macrophages, which produce MMP enzymes. In another animal model, the blood transfer model, f-NPs potently suppressed the establishment of tumor foci in lung. Based on these data, we conclude that f-NPs have antimetastasis effects and speculate that utilization of f-NPs may provide a new strategy for the treatment of tumor metastasis.
From the Clinical Editor
In this study utilizing metallofullerenol nanoparticles, the authors demonstrate antimetastasis effects and speculate that utilization of these nanoparticles may provide a new strategy in metastatic tumor therapy.
Graphical Abstract
Gadolinium metallofullerenol nanoparticles inhibit cancer metastasis through matrix metalloproteinase inhibition: imprisoning instead of poisoning cancer cells.
Key words: Nanomedicine, Metallofullerenol nanoparticles, Cancer metastasis, Matrix metalloproteinase, Fibrous cage
The authors thank for the support of MOST 973 program (2009CB930204, 2011CB933403, 2010CB934000, 2012CB934000) and CAS Knowledge Innovation Program. This study was partly funded by National Natural Science Foundation of China (10875136), and U.S NIH/RCMI/NCRR (2G12RR003048) and DOD (W81XWH-10-1-0767). M.F., T.S., E.B., are grateful for the support of the U.S. DoD Innovator Award (W81XWH-09-1-0212), NIH U54CA143837 and U54CA151668, and the Ernest Cockrell Jr. Distinguished Endowed Chair.
PII: S1549-9634(11)00356-X
doi:10.1016/j.nano.2011.08.019
© 2012 Elsevier Inc. All rights reserved.
Volume 8, Issue 2 , Pages 136-146, February 2012

