| Literature DB >> 26806362 |
Janine N Boodram1, Iain J Mcgregor1, Peter M Bruno2, Paul B Cressey1, Michael T Hemann2, Kogularamanan Suntharalingam3.
Abstract
The breast cancer stem cell (CSC) potency of a series of copper(II)-phenanthroline complexes containing the nonsteroidal anti-inflammatory drug (NSAID), indomethacin, is reported. The most effective copper(II) complex in this series, 4, selectivity kills breast CSC-enriched HMLER-shEcad cells over breast CSC-depleted HMLER cells. Furthermore, 4 reduces the formation, size, and viability of mammospheres, to a greater extent than salinomycin, a potassium ionophore known to selectively inhibit CSCs. Mechanistic studies revealed that the CSC-specificity observed for 4 arises from its ability to generate intracellular reactive oxygen species (ROS) and inhibit cyclooxygenase-2 (COX-2), an enzyme that is overexpressed in breast CSCs. The former induces DNA damage, activates JNK and p38 pathways, and leads to apoptosis.Entities:
Keywords: COX inhibition; bioinorganic chemistry; cancer; nonsteroidal anti-inflammatory drugs; reactive oxygen species
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Year: 2016 PMID: 26806362 DOI: 10.1002/anie.201510443
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336