G2/M-Phase-Inhibitory Mitochondrial-Depolarizing Re(I)/Ru(II)/Ir(III)-2,2'-Bipyrimidine-Based Heterobimetallic Luminescent Complexes: An Assessment of In Vitro Antiproliferative Activity and Bioimaging for Targeted Therapy toward Human TNBC Cells.
Nilmadhab RoyShanooja ShanavasBinoy KarLavanya Thilak BabuUtpal DasPothabathula Seshu VardhanSuban Kumar SahooBipasha BoseVijayaraghavan RPriyankar PairaPublished in: ACS omega (2023)
Triple-negative breast cancer (TNBC) is an extremely vicious subtype of human breast cancer having the worst prognosis along with strong invasive and metastatic competency. Hence, it can easily invade into blood vessels, and presently, no targeted therapeutic approach is available to annihilate this type of cancer. Metal complexes have successfully stepped into the anticancer research and are now being applauded due to their anticancer potency after the discovery of cisplatin. Many of these metal complexes are also well recognized for their activity toward breast cancer. As the TNBC is a very dangerous subtype and has long been a challenging ailment to treat, we have intended to develop a few brand new mixed metallic Ru(II)/Ir(III)/Re(I)-2,2'-bipyrimidine complexes [ L'Re2 ], [ L'RuRe ], and [ L'IrRe ] to abate the unbridled proliferation of TNBC cells. The potency of the complexes against TNBC cells has been justified using MDA-MB-468 TNBC cell lines where complex [ L'IrRe ] has displayed significant potency among all the three complexes with an IC 50 value of 24.12 μM. The complex [ L'IrRe ] has been competent to cause apoptosis of TNBC cells through inhibition of the G2/M phase in the cell cycle in association with a profuse amount of ROS generation and mitochondrial depolarization.
Keyphrases
- cell cycle arrest
- induced apoptosis
- cell death
- oxidative stress
- cell cycle
- endoplasmic reticulum stress
- endothelial cells
- pi k akt
- cell proliferation
- randomized controlled trial
- small cell lung cancer
- signaling pathway
- dna damage
- small molecule
- quantum dots
- young adults
- breast cancer cells
- high throughput
- papillary thyroid