Gd-metallofullerenol nanomaterial as non-toxic breast cancer stem cell-specific inhibitor

Ying Liu(Chinese Academy of Sciences), Chunying Chen(Chinese Academy of Sciences), Pengxu Qian(University of Science and Technology of China), Xuefei Lu(University of Science and Technology of China), Baoyun Sun(Chinese Academy of Sciences), Xiao Zhang(University of Science and Technology of China), Liming Wang(Chinese Academy of Sciences), Xingfa Gao(Chinese Academy of Sciences), Li Han(Chinese Academy of Sciences), Zhiyun Chen(Chinese Academy of Sciences), Jinglong Tang(Chinese Academy of Sciences), Weijie Zhang(University of Science and Technology of China), Jinquan Dong(Chinese Academy of Sciences), Ru Bai(Chinese Academy of Sciences), Peter E. Lobie(University of Science and Technology of China), Qingfa Wu(University of Science and Technology of China), Suling Liu(University of Science and Technology of China), Huafeng Zhang(University of Science and Technology of China), Feng Zhao(Chinese Academy of Sciences), Max S. Wicha(University of Michigan), Tao Zhu(University of Science and Technology of China), Yuliang Zhao(Chinese Academy of Sciences)
Nature Communications
January 23, 2015
Cited by 203Open Access
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Abstract

The contemporary use of nanomedicines for cancer treatment has been largely limited to serving as carriers for existing therapeutic agents. Here, we provide definitive evidence that, the metallofullerenol nanomaterial Gd@C82(OH)22, while essentially not toxic to normal mammary epithelial cells, possesses intrinsic inhibitory activity against triple-negative breast cancer cells. Gd@C82(OH)22 blocks epithelial-to-mesenchymal transition with resultant efficient elimination of breast cancer stem cells (CSCs) resulting in abrogation of tumour initiation and metastasis. In normoxic conditions, Gd@C82(OH)22 mediates these effects by blocking TGF-β signalling. Moreover, under hypoxic conditions found in the tumour microenvironment, cellular uptake of Gd@C82(OH)22 is facilitated where it functions as a bi-potent inhibitor of HIF-1α and TGF-β activities, enhancing CSC elimination. These studies indicate that nanomaterials can be engineered to directly target CSCs. Thus, Gd-metallofullerenol is identified as a kind of non-toxic CSC specific inhibitors with significant therapeutic potential.


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