| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1301357 | Inorganic Chemistry Communications | 2015 | 4 Pages |
•A novel cyclometalated iridium(III) complex, [Ir(CˆN)2(HPIP)]Cl (IrC) exhibited about 10-fold higher cytotoxicity than cisplatin against A549 cancer cell line.•A cisplatin-resistant cell line, A549-CP/R was showed sensitivity to IrC.
A novel cyclometalated iridium(III) complex, [Ir(CˆN)2(HPIP)]Cl (IrC) was synthesized and characterized. IrC exhibited about 10-fold higher cytotoxicity than cisplatin against A549 cancer cell line. Interestingly, a cisplatin-resistant cell line, A549-CP/R showed sensitivity to IrC. Further study suggested that IrC induced apoptosis via negatively regulated the nuclear factor-kappa B (NF-κB) pathway, which involved reactive oxygen species (ROS) generation, Bcl-2 and caspase family members activation. Taken together, these results suggest that IrC is able to overcome chemoresistance and may be an effective treatment for platinum-resistant cancer therapy.
Graphical abstractA novel cyclometalated iridium(III) complex avoids cisplatin resistance and induces apoptosis via the nuclear factor-κB/reactive oxygen species pathway in A549 cisplatin-resistant human lung cancer cells.Figure optionsDownload full-size imageDownload as PowerPoint slide
