Cytotoxic rhodium(III) and iridium(III) polypyridyl Complexes: Structure-activity relationships, antileukemic activity, and apoptosis induction

Abstract

Meridional rhodium(III) polypyridyl complexes of the type mer- [RhX 3(DMSO)(pp)] (X = Cl, pp=phen 1, dpq 2, dppz 3;X = Br, pp=phen 4) represent a promising class of potent cytostatic agents for the treatment of lymphoma and leukemia. Exposure of their DMSO solutions to light leads to slow isomerization to mixtures of the mer and the generally less active fac isomers. As a result, the IC50 values of 1 and 2 toward HT-29 cells increase from 0.19 and 0.069 μm on immediate use in the dark to 0.66 and 0.312 μm, respectively, after exposure of their DMSO stock solutions to light for 7 days. In striking contrast, the complexes mer-[IrX3(DMSO)(phen)] (X = Cl 7,Br 8) are significantly less cytotoxic than their facial IrIII polypyridyl counterparts: IC50 = 20.3 μm for 7 and 4.6 μm for fac-[IrCl3(DMSO)(phen)] 5 toward MCF-7 cells. The IC50 values for the complexes fac-[IrX3(L)(pp)] 9-13 decrease in the orders: a) Cl> DMSO for L. Specific apoptotic cell death by DNA fragmentation was detected for leukemia (NALM-6) and lymphoma (BJAB) cells after incubation with 2, 3, and 11 (X= Br, L = H 2O, pp= phen) for 72 h. Loss of the mitochondrial membrane potential in lymphoma cells indicates that apoptosis is mediated via the intrinsic mitochondrial pathway. LDH release assays after 1 or 3 h demonstrate that necrotic damage is negligible. © 2009 Wiley-VCH Verlag GmbH&Co. KGaA, Weinheim.