The preparation of multi-nuclear metal complexes offers a route to novel anticancer agents and delivery systems. The potency of a novel triangular multi-nuclear complex containing three platinum atoms, Pt-3, towards breast cancer stem cells (CSCs) is reported. The tri-nuclear platinum(II) complex, Pt-3 exhibits selectivity toxicity towards breast CSCs over bulk breast cancer cells and non-tumorigenic breast cells. Remarkably, Pt-3 inhibits the formation, size, and viability of mammospheres to a better extent than salinomycin, an established CSC-potent agent, and cisplatin and carboplatin, clinically used platinum drugs. Mechanism of action studies show that Pt-3 effectively enters breast CSCs, penetrates the nucleus, induces genomic DNA damage, and prompts caspase-dependent apoptosis. To the best of our knowledge, Pt-3 is the first multi-nuclear platinum complex to selectivity kill breast CSCs over other breast cell types.
Funding
K.S. was supported by a Leverhulme Early Career Fellowship
(ECF-2014-178). S.G. is funded by a UGC start-up grant (F.4-
5/2006, BSR) and the Newton Alumni Fund. A.E. is supported
by a KCL studentship. Thanks to Dr. Biswajit Bhattacharya
(BAM Federal Institute for Materials Research and Testing) for
useful discussions and suggestions with respect to the X-ray
crystallography studies. We are grateful to Prof. Robert
Weinberg (Whitehead Institute, MIT) for providing the cell lines
used in this study.
History
Citation
Angewandte Chemie International Edition, 2019
Author affiliation
/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistry
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