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    <subfield code="a">10.1021/acs.inorgchem.0c02922</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">Mármol, I.</subfield>
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    <subfield code="a">Gold(I) and Silver(I) Complexes with 2-Anilinopyridine-Based Heterocycles as Multitarget Drugs against Colon Cancer</subfield>
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    <subfield code="c">2020</subfield>
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    <subfield code="a">A series of gold(I) and silver(I) derivatives with N- or S-donor ligands derived from 2-anilinopyridine has been synthesized and characterized. The mononuclear structure of [Au(L1)(PPh3)](TfO) (1a) and [Au(L2)(PPh3)](TfO) (1b) was confirmed by X-ray diffraction studies, as well as the dinuclear structure in the case of [Ag(TfO)(L1)]2 (4a). Most of the complexes are cytotoxic against a model of colorectal adenocarcinoma (Caco-2 cell line) and breast adenocarcinoma cancer cell lines (MCF-7). [Au(L1)(PPh3)](TfO) (1a) was able to induce caspases 8 and 3 activation, loss of mitochondrial membrane potential, and reactive oxygen species (ROS)-dependent cell death on Caco-2 cells upon 24 h incubation. In addition, the gold complex 1a produced a significant inhibition of the redox enzyme thioredoxin reductase as well as 20S proteasome. However, the silver(I) analogue, [Ag(TfO)(L1)(PPh3)] (2a), induced cell death independent of inhibition of thioredoxin reductase and 20S proteasome, triggered ROS-independent apoptosis mediated by caspase 8 and 3 activation, and loss of mitochondrial membrane potential, which points to a different mechanism of action for both derivatives, dependent on the metal center.</subfield>
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    <subfield code="a">Physical and Theoretical Chemistry</subfield>
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    <subfield code="a">Inorganic Chemistry</subfield>
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    <subfield code="a">Montanel-Perez, S.</subfield>
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    <subfield code="a">Royo, J.C.</subfield>
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    <subfield code="a">Gimeno, M.C.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="a">Villacampa, M.D.</subfield>
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    <subfield code="a">Cerrada, E.</subfield>
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    <subfield code="1">2010</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
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    <subfield code="c">Área Fisiología</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">59, 23 (2020), 17732-17745</subfield>
    <subfield code="p">Inorg. chem.</subfield>
    <subfield code="t">Inorganic Chemistry</subfield>
    <subfield code="x">0020-1669</subfield>
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