Antiproliferative Homoleptic and Heteroleptic Phosphino Silver(I) Complexes: Effect of Ligand Combination on Their Biological Mechanism of Action
A series of neutral mixed-ligand [HB(pz) ]Ag(PR ) silver(I) complexes (PR = tertiary phosphine, [HB(pz) ] = tris(pyrazolyl)borate anion), and the corresponding homoleptic [Ag(PR ) ]BF compounds have been synthesized and fully characterized. Silver compounds were screened for their antiproliferative...
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Published in | Molecules (Basel, Switzerland) Vol. 25; no. 22; p. 5484 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI AG
23.11.2020
MDPI |
Subjects | |
Online Access | Get full text |
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Summary: | A series of neutral mixed-ligand [HB(pz)
]Ag(PR
) silver(I) complexes (PR
= tertiary phosphine, [HB(pz)
]
= tris(pyrazolyl)borate anion), and the corresponding homoleptic [Ag(PR
)
]BF
compounds have been synthesized and fully characterized. Silver compounds were screened for their antiproliferative activities against a wide panel of human cancer cells derived from solid tumors and endowed with different platinum drug sensitivity. Mixed-ligand complexes were generally more effective than the corresponding homoleptic derivatives, but the most active compounds were [HB(pz)
]Ag(PPh
) (
) and [Ag(PPh
)
]BF
(
), both comprising the lipophilic PPh
phosphine ligand. Detailed mechanistic studies revealed that both homoleptic and heteroleptic silver complexes strongly and selectively inhibit the selenoenzyme thioredoxin reductase both as isolated enzyme and in human ovarian cancer cells (half inhibition concentration values in the nanomolar range) causing the disruption of cellular thiol-redox homeostasis, and leading to apoptotic cell death. Moreover, for heteroleptic Ag(I) derivatives, an additional ability to damage nuclear DNA has been detected. These results confirm the importance of the type of silver ion coordinating ligands in affecting the biological behavior of the overall corresponding silver complexes, besides in terms of hydrophilic-lipophilic balance, also in terms of biological mechanism of action, such as interaction with DNA and/or thioredoxin reductase. |
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ISSN: | 1420-3049 1420-3049 |
DOI: | 10.3390/molecules25225484 |