A comparison of novel organoiridium(III) complexes and their ligands as a potential treatment for prostate cancer


Autoria(s): Hockey, Samantha C.; Barbante, Gregory J.; Francis, Paul S.; Altimari, Jarrad M.; Yoganantharajah, Prusothman; Gibert, Yann; Henderson, Luke C.
Data(s)

15/02/2016

Resumo

A range of 1,4-substituted 2-pyridyl-N-phenyl triazoles were synthesised and evaluated for their antiproliferative properties against lymph node cancer of the prostate (LNCaP) and bone metastasis of prostate cancer (PC-3) cells. Excellent-to-low IC50 values were determined (5.6-250 μM), and a representative group of 4 ligands were then complexed to iridium(III) giving highly luminescent species. Re-evaluation of these compounds against both cell lines was then undertaken and improved potency (up to 72-fold) was observed, giving IC50 values of 0.36-11 μM for LNCaP and 0.85-5.9 μM for PC-3. Preliminary screens for in vivo toxicity were conducted using a zebrafish model showing a wide range of induced toxicity depending of the compound evaluated. Apoptosis and Caspase-3 levels were also determined and showed no statistical difference between some of the treated specimens and the controls. This study may identify novel therapeutic agents for advanced stage of prostate cancer in humans.

Identificador

http://hdl.handle.net/10536/DRO/DU:30081052

Idioma(s)

eng

Publicador

Elsevier

Relação

http://dro.deakin.edu.au/eserv/DU:30081052/hockey-comparisonnovel-2016.pdf

http://www.dx.doi.org/10.1016/j.ejmech.2015.12.035

Direitos

2016, Elsevier

Palavras-Chave #Click chemistry #Iridium #Prostate cancer #Triazole
Tipo

Journal Article