2-Aryl-1 H -imidazo[4,5- f ][1,10]phenanthroline-Based Binuclear Ru(II)/Ir(III)/Re(I) Complexes as Mitochondria Targeting Cancer Stem Cell Therapeutic Agents.
Binoy KarShanooja ShanavasArun KarmakarApoorva H NagendraPothabathula Seshu VardhanSuban Kumar SahooBipasha BoseSubrata KunduPriyankar PairaPublished in: Journal of medicinal chemistry (2024)
A series of novel Ru(II)/Ir(III)/Re(I)-based organometallic complexes [ Ru 2 L1 , Ru 2 L2 , Ir 2 L1 , Ir 2 L2 , Re 2 L1 , and Re 2 L2 ] have been synthesized to assess their potency and selectivity against multiple cancer cells A549, HCT-116, and HCT-116 colon CSCs. The cytotoxic screening of the synthesized complexes has revealed that complex Ru 2 L1 and Ir 2 L2 are two proficient complexes among all, but Ru 2 L1 is the most potent complex. A significant binding constant value was observed for DNA and BSA in all complexes. Significant lipophilic properties allow them to penetrate cancer cell membranes, and substantial quantum yield (ϕ f ) values support bioimaging potential. Again, these complexes are particular for mitochondrial localization and produce a profuse amount of ROS to damage the mitochondrial DNA and then G1 phase cell-cycle arrest. Protein expression analysis unveiled that pro-apoptotic Bax protein overexpressed in Ru 2 L1 -treated cells, whereas antiapoptotic Bcl-2 protein was expressed twofold in Ir 2 L2 -treated cells, which correlated with autophagy reticence.
Keyphrases
- cell cycle arrest
- cell death
- energy transfer
- mitochondrial dna
- pi k akt
- induced apoptosis
- oxidative stress
- cancer stem cells
- signaling pathway
- copy number
- binding protein
- quantum dots
- gene expression
- endoplasmic reticulum stress
- anti inflammatory
- amino acid
- molecular dynamics
- dna damage
- reactive oxygen species
- small molecule
- cancer therapy
- fluorescent probe
- newly diagnosed
- human health
- endoplasmic reticulum