| Literature DB >> 27038531 |
Maura Montani1, Gretta V Badillo Pazmay2, Albana Hysi3, Giulio Lupidi4, Riccardo Pettinari5, Valentina Gambini1, Martina Tilio1, Fabio Marchetti6, Claudio Pettinari5, Stefano Ferraro6, Manuela Iezzi3, Cristina Marchini1, Augusto Amici7.
Abstract
Ruthenium compounds have become promising alternatives to platinum drugs by displaying specific activities against different cancers and favorable toxicity and clearance properties. Here, we show that the ruthenium(II) complex [Ru(p-cymene)(bis(3,5-dimethylpyrazol-1-yl)methane)Cl]Cl (UNICAM-1) exhibits potent in vivo antitumor effects. When administered as four-dose course, by repeating a single dose (52.4mgkg-1) every three days, UNICAM-1 significantly reduces the growth of A17 triple negative breast cancer cells transplanted into FVB syngeneic mice. Pharmacokinetic studies indicate that UNICAM-1 is rapidly eliminated from kidney, liver and bloodstream thanks to its high hydrosolubility, exerting excellent therapeutic activity with minimal side effects. Immunohistological analysis revealed that the efficacy of UNICAM-1, mainly relies on its capacity to reverse tumor-associated immune suppression by significantly reducing the number of tumor-infiltrating regulatory T cells. Therefore, UNICAM-1 appears very promising for the treatment of TNBC.Entities:
Keywords: Anticancer drugs; In vivo tests; Organometallic arene complexes; Ruthenium(II); Triple negative breast cancer; Tumor infiltrating regulatory T cells
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Year: 2016 PMID: 27038531 DOI: 10.1016/j.phrs.2016.03.032
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658