| Literature DB >> 32438200 |
Natalia Sanz Del Olmo1, Ana M Bajo2, Maksim Ionov3, Sandra García-Gallego1, Maria Bryszewska3, Rafael Gómez4, Paula Ortega5, F Javier de la Mata6.
Abstract
In searching for efficient and selective antitumour drugs, a new family of carbosilane metallodendrimers functionalized with [Ru(η5-C5H5)(PTA)Cl] (PTA = 1,3,5-triaza-7-phosphatricyclo-[3.3.1.1] decane) is reported. Experiments of the biophysical characterization showed an ability to interact with biological membranes, as well as with proteins (e.g. human serum albumin) without affecting their usual biological activity. These metallodendrimers possessed potent and selective anticancer activity in vitro in a panel of tumour cell lines. Importantly, the first generation metallodendrimer, bearing 4 Ru(II) complexes, was remarkably active towards resistant prostate cancer cells, inhibiting both cell proliferation and metastasis to bone tissues. Such promising antitumour activity can be further improved when given with docetaxel, with in vitro cytotoxicity being in the nanomolar range. Furthermore, its intravenous administration to an advanced prostate cancer mice model inhibited tumour growth up to 25% and 45% when given 10 mg/kg/week and 7.5 mg/kg/4-5 days, respectively.Entities:
Keywords: Antitumour; Combination-therapy; Cyclopentadienyl; Dendrimer; PTA; Ruthenium
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Year: 2020 PMID: 32438200 DOI: 10.1016/j.ejmech.2020.112414
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514