» Articles » PMID: 28654103

The Development of Anticancer Ruthenium(ii) Complexes: from Single Molecule Compounds to Nanomaterials

Overview
Journal Chem Soc Rev
Specialty Chemistry
Date 2017 Jun 28
PMID 28654103
Citations 186
Authors
Affiliations
Soon will be listed here.
Abstract

Cancer is rapidly becoming the top killer in the world. Most of the FDA approved anticancer drugs are organic molecules, while metallodrugs are very scarce. The advent of the first metal based therapeutic agent, cisplatin, launched a new era in the application of transition metal complexes for therapeutic design. Due to their unique and versatile biochemical properties, ruthenium-based compounds have emerged as promising anti-cancer agents that serve as alternatives to cisplatin and its derivertives. Ruthenium(iii) complexes have successfully been used in clinical research and their mechanisms of anticancer action have been reported in large volumes over the past few decades. Ruthenium(ii) complexes have also attracted significant attention as anticancer candidates; however, only a few of them have been reported comprehensively. In this review, we discuss the development of ruthenium(ii) complexes as anticancer candidates and biocatalysts, including arene ruthenium complexes, polypyridyl ruthenium complexes, and ruthenium nanomaterial complexes. This review focuses on the likely mechanisms of action of ruthenium(ii)-based anticancer drugs and the relationship between their chemical structures and biological properties. This review also highlights the catalytic activity and the photoinduced activation of ruthenium(ii) complexes, their targeted delivery, and their activity in nanomaterial systems.

Citing Articles

Hybrid Materials Based on Reduced Graphene Oxide; Synthesis and Characterization of V and Ru Metal Complexes.

Bal M, Tontus M, Tumer M J Fluoresc. 2025; .

PMID: 39939500 DOI: 10.1007/s10895-025-04184-3.


Ruthenium(II) Complex with 1-Hydroxy-9,10-Anthraquinone Inhibits Cell Cycle Progression at G0/G1 and Induces Apoptosis in Melanoma Cells.

Dias J, Ferreira-Silva G, Viana R, de Araujo Neto J, Ellena J, Correa R Pharmaceuticals (Basel). 2025; 18(1).

PMID: 39861126 PMC: 11768811. DOI: 10.3390/ph18010063.


A Novel Substituted Benzo[]quinoxaline-Based Cyclometalated Ru(II) Complex as a Biocompatible Membrane-Targeted PDT Colon Cancer Stem Cell Agent.

Marco A, Kasparkova J, Bautista D, Kostrhunova H, Cutillas N, Markova L J Med Chem. 2024; 67(23):21470-21485.

PMID: 39620973 PMC: 11647881. DOI: 10.1021/acs.jmedchem.4c02357.


Multifunctional nanocomposites utilizing ruthenium (II) complex/manganese (IV) dioxide nanoparticle for synergistic reinforcing radioimmunotherapy.

Peng J, Quan D, Yang G, Wei L, Yang Z, Dong Z J Nanobiotechnology. 2024; 22(1):735.

PMID: 39593029 PMC: 11600833. DOI: 10.1186/s12951-024-03013-2.


Light enhanced cytotoxicity and antitumoral effect of a ruthenium-based photosensitizer inspired from natural alkaloids.

Sanita G, Alfieri M, Carrese B, Damian S, Mele V, Cali G RSC Med Chem. 2024; .

PMID: 39553466 PMC: 11565246. DOI: 10.1039/d4md00600c.


References
1.
Therrien B, Suss-Fink G, Govindaswamy P, Renfrew A, Dyson P . The "complex-in-a-complex" cations [(acac)2M subset Ru6(p-iPrC6H4Me)6(tpt)2(dhbq)3]6+: A trojan horse for cancer cells. Angew Chem Int Ed Engl. 2008; 47(20):3773-6. DOI: 10.1002/anie.200800186. View

2.
Fetzer L, Boff B, Ali M, Xiangjun M, Collin J, Sirlin C . Library of second-generation cycloruthenated compounds and evaluation of their biological properties as potential anticancer drugs: passing the nanomolar barrier. Dalton Trans. 2011; 40(35):8869-78. DOI: 10.1039/c1dt10322a. View

3.
Pacor S, Zorzet S, Cocchietto M, Bacac M, Vadori M, Turrin C . Intratumoral NAMI-A treatment triggers metastasis reduction, which correlates to CD44 regulation and tumor infiltrating lymphocyte recruitment. J Pharmacol Exp Ther. 2004; 310(2):737-44. DOI: 10.1124/jpet.104.066175. View

4.
Bacac M, Hotze A, van der Schilden K, Haasnoot J, Pacor S, Alessio E . The hydrolysis of the anti-cancer ruthenium complex NAMI-A affects its DNA binding and antimetastatic activity: an NMR evaluation. J Inorg Biochem. 2004; 98(2):402-12. DOI: 10.1016/j.jinorgbio.2003.12.003. View

5.
He S, Krippes K, Ritz S, Chen Z, Best A, Butt H . Ultralow-intensity near-infrared light induces drug delivery by upconverting nanoparticles. Chem Commun (Camb). 2014; 51(2):431-4. DOI: 10.1039/c4cc07489k. View