Anticancer organometallic half-sandwich complexes of estrone-derived (N,N) donor ligands with enhanced aqueous solubility

Author(s): Tamás Pivarcsik, Ferenc Kovács, Gabriella Spengler, Márta Nové, Bernhard K. Keppler, Wolfgang Kandioller, Éva Frank, Éva A. Enyedy
Abstract: Four steroidal derivatives (L^1-4) bearing an (N,N) metal-chelating subunit on the D-ring, in addition to the organometallic [M(arene)(N,N)Cl]Cl complexes of L^1,2 were synthesized and characterized, in which M(arene) is Rh(III)(η⁵-C₅Me₅) or Ir(III)(η⁵-C₅Me₅) or Ru(II)(η⁶-p-cymene). The solution chemical properties of both the estrone-based ligands and selected complexes were investigated by spectroscopic methods. At pH = 7.4, the ligands are predominantly positively charged, moderately lipophilic (logD_7.4 = +0.6 − +3.2), and exhibit low-to-medium micromolar solubility (S_7.4 = 9–543 μM) and are more hydrophilic than estrone; however, complexation improved the aqueous solubility of the obtained organometallics. The Rh(η⁵-C₅Me₅) and Ru(η⁶-p-cymene) complexes of L¹ demonstrated high stability in solution (<1 % bidentate ligand dissociation at pH 7.4 for 48 h), forming a higher fraction of mixed hydroxido species [M(arene)(N,N)(OH)]⁺ in the case of the Ru complexes. Both coordination and intermolecular interactions of the organometallic complexes with human serum albumin were observed. The ligands and their complexes were tested in human cancer cell lines to investigate their in vitro anticancer activity. Studies in Colo-205 and MCF-7 cells revealed the moderate-to-strong cytotoxicity of the ligands (IC₅₀ = 5–50 μM) with limited selectivity toward cancer cells over the non-cancerous CCD-19Lu fibroblast cell line. Complexation increased the cytotoxicity, especially for Rh(III)(η⁵-C₅Me₅) and Ir(III)(η⁵-C₅Me₅) complexes in the MCF-7 cell line compared to the ligands.
Organisation(s): Department of Inorganic Chemistry
External organisation(s): University of Szeged, Research Cluster Translational Cancer Therapy Research
Journal: Journal of Inorganic Biochemistry
Volume: 267
ISSN: 0162-0134
DOI: https://doi.org/10.1016/j.jinorgbio.2025.112858
Publication date: 06-2025
Peer reviewed: Yes
Austrian Fields of Science 2012: 104003 Inorganic chemistry, 106002 Biochemistry, 301904 Cancer research
Keywords
ASJC Scopus subject areas: Biochemistry, Inorganic Chemistry
Sustainable Development Goals: SDG 3 - Good Health and Well-being
Portal url: https://ucrisportal.univie.ac.at/en/publications/d74ce616-c826-447d-a33b-3c1c69ca24ac