Membrane localized iridium(III) complex induces endoplasmic reticulum stress and mitochondria-mediated apoptosis in human cancer cells.

Abstract

The cellular behavior and toxicity effect of organometallic complexes depend largely on their peripheral ligands. In this study, we have synthesized a series of novel luminescent cationic iridium(III) complexes by tuning the ancillary N(∧)N ligand based on a structure [Ir(ppy)2(N(∧)N)](+) (ppy = 1-phenyl-pyridine; N(∧)N = 2,2'-bipyridine (bpy, 1) or phenanthroline (phen, 2) or 4,7-diphenyl-1,10- phenanthroline (DIP, 3)). As the size of coordinated N(∧)N ligand increases, absorbance/emission efficiency, quantum yields, lipophilicity, and cell uptake rates of the complexes also increase, in a general order: 3 > 2 > 1. All three complexes display anticancer activity, with 3 exhibiting the highest cellular uptake efficiency and the greatest cytotoxic activities in several cancer cell lines with IC50s lower than that of cisplatin. Because of its strong hydrophobic nature, the death inducer 3 was found to accumulate favorably to endoplasmic reticulum (ER) and to cause ER stress in cells. The fast cytosolic release of calcium from stressed ER disturbed the morphology and function of mitochondria, initiating an intrinsic apoptotic pathway. Understanding of the cell death mechanism would help further structure-activity optimization on these novel Ir(III) complexes as emerging cancer therapeutics.

• Authors: Rui Cao, Junli Jia, Xiaochuan Ma, Ming Zhou, Hao Fei
• Journal: Journal of medicinal chemistry (J Med Chem) Vol. 56 Issue 9 Pg. 3636-44 (May 09 2013) ISSN: 1520-4804 [Electronic] United States
• PMID: 23594206 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• Ligands
• Organometallic Compounds
• Iridium

Topics

• Antineoplastic Agents (chemistry, metabolism, pharmacology)
• Apoptosis (drug effects)
• Biological Transport
• Cell Line, Tumor
• Cell Membrane (drug effects, metabolism)
• Endoplasmic Reticulum Stress (drug effects)
• Humans
• Hydrophobic and Hydrophilic Interactions
• Inhibitory Concentration 50
• Iridium (chemistry)
• Ligands
• Mitochondria (drug effects, metabolism)
• Organometallic Compounds (chemistry, metabolism, pharmacology)