On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions
A series of cyclometallated platinum(IV) compounds (3a, 3a' and 3b') with a meridional [C,N,N'] terdentate ligand, featuring an halido and an aryl group in the axial positions has been evaluated for electrochemical reduction and preliminary biological behavior against a panel of human...
| Autores: | , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2016 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2445/165158 |
| Acceso en línea: | https://hdl.handle.net/2445/165158 |
| Access Level: | acceso abierto |
| Palabra clave: | Platí Medicaments antineoplàstics Platinum Antineoplastic agents |
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On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positionsEscolà Jané, AnnaCrespo Vicente, Margarita Ma.López Martínez, Ma. ConcepciónQuirante Serrano, JosefinaJayaraman, AnushaHalil Polat, IbrahimBadía Palacín, JosefaBaldomà Llavinés, LauraCascante i Serratosa, MartaPlatíMedicaments antineoplàsticsPlatinumAntineoplastic agentsA series of cyclometallated platinum(IV) compounds (3a, 3a' and 3b') with a meridional [C,N,N'] terdentate ligand, featuring an halido and an aryl group in the axial positions has been evaluated for electrochemical reduction and preliminary biological behavior against a panel of human adenocarcinoma (A-549 lung, HCT-116 colon, and MCF-7 breast) cell lines and the normal bronquial epithelial BEAS-2B cells. Cathodic reduction potentials (shifting from -1.463 to -1.570 V) reveal that the platinum(IV) compounds under study would be highly reluctant to be reduced in a biological environment. Actually ascorbic acid was not able to reduce complex 3a', the most prone to be reduced according its reduction potential, over a period of one week. These results suggest an intrinsic activity for the investigated platinum(IV) complexes (3a, 3a' and 3b'), which exhibit a remarkable cytotoxicity effectiveness (with IC50 values in the low micromolar range), even greater than that of cisplatin. The IC50 for A-549 lung cells and clog P values were found to follow the same trend: 3b' > 3a' > 3a. However, no correlation was observed between reduction potential and in vitro activity. As a representative example, cyclometallated platinum(IV) compound 3a', exercise its antiproliferative activity directly over non-microcytic A-549 lung cancer cells through a mixture of cell cycle arrest (13% arrest at G1 phase and 46% arrest at G2 phase) and apoptosis induction (increase of early apoptosis by 30 times with regard to control). To gain further insights into the mode of action of the investigated platinum(IV) complexes, drug uptake, cathepsin B inhibition and ROS generation were also evaluated. Interestingly an increased ROS generation could be related with the antiproliferative activity of the cyclometallated platinum(IV) series under study in the cisplatin-resistant A-549 lung and HCT-116 cancer cell lines.Elsevier Ltd2020202020162020info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersion12 p.application/pdfhttps://hdl.handle.net/2445/165158Articles publicats en revistes (Química Inorgànica i Orgànica)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésVersió postprint del document publicat a: https://doi.org/10.1016/j.bmc.2016.09.037Bioorganic & Medicinal Chemistry, 2016, vol. 24, num. 22, p. 5804-5815https://doi.org/10.1016/j.bmc.2016.09.037cc-by-nc-nd (c) Elsevier Ltd, 2016http://creativecommons.org/licenses/by-nc-nd/3.0/esinfo:eu-repo/semantics/openAccessoai:recercat.cat:2445/1651582026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions |
| title |
On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions |
| spellingShingle |
On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions Escolà Jané, Anna Platí Medicaments antineoplàstics Platinum Antineoplastic agents |
| title_short |
On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions |
| title_full |
On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions |
| title_fullStr |
On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions |
| title_full_unstemmed |
On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions |
| title_sort |
On the stability and biological behavior of cyclometallated Pt(IV) complexes with halido and aryl ligands in the axial positions |
| dc.creator.none.fl_str_mv |
Escolà Jané, Anna Crespo Vicente, Margarita Ma. López Martínez, Ma. Concepción Quirante Serrano, Josefina Jayaraman, Anusha Halil Polat, Ibrahim Badía Palacín, Josefa Baldomà Llavinés, Laura Cascante i Serratosa, Marta |
| author |
Escolà Jané, Anna |
| author_facet |
Escolà Jané, Anna Crespo Vicente, Margarita Ma. López Martínez, Ma. Concepción Quirante Serrano, Josefina Jayaraman, Anusha Halil Polat, Ibrahim Badía Palacín, Josefa Baldomà Llavinés, Laura Cascante i Serratosa, Marta |
| author_role |
author |
| author2 |
Crespo Vicente, Margarita Ma. López Martínez, Ma. Concepción Quirante Serrano, Josefina Jayaraman, Anusha Halil Polat, Ibrahim Badía Palacín, Josefa Baldomà Llavinés, Laura Cascante i Serratosa, Marta |
| author2_role |
author author author author author author author author |
| dc.subject.none.fl_str_mv |
Platí Medicaments antineoplàstics Platinum Antineoplastic agents |
| topic |
Platí Medicaments antineoplàstics Platinum Antineoplastic agents |
| description |
A series of cyclometallated platinum(IV) compounds (3a, 3a' and 3b') with a meridional [C,N,N'] terdentate ligand, featuring an halido and an aryl group in the axial positions has been evaluated for electrochemical reduction and preliminary biological behavior against a panel of human adenocarcinoma (A-549 lung, HCT-116 colon, and MCF-7 breast) cell lines and the normal bronquial epithelial BEAS-2B cells. Cathodic reduction potentials (shifting from -1.463 to -1.570 V) reveal that the platinum(IV) compounds under study would be highly reluctant to be reduced in a biological environment. Actually ascorbic acid was not able to reduce complex 3a', the most prone to be reduced according its reduction potential, over a period of one week. These results suggest an intrinsic activity for the investigated platinum(IV) complexes (3a, 3a' and 3b'), which exhibit a remarkable cytotoxicity effectiveness (with IC50 values in the low micromolar range), even greater than that of cisplatin. The IC50 for A-549 lung cells and clog P values were found to follow the same trend: 3b' > 3a' > 3a. However, no correlation was observed between reduction potential and in vitro activity. As a representative example, cyclometallated platinum(IV) compound 3a', exercise its antiproliferative activity directly over non-microcytic A-549 lung cancer cells through a mixture of cell cycle arrest (13% arrest at G1 phase and 46% arrest at G2 phase) and apoptosis induction (increase of early apoptosis by 30 times with regard to control). To gain further insights into the mode of action of the investigated platinum(IV) complexes, drug uptake, cathepsin B inhibition and ROS generation were also evaluated. Interestingly an increased ROS generation could be related with the antiproliferative activity of the cyclometallated platinum(IV) series under study in the cisplatin-resistant A-549 lung and HCT-116 cancer cell lines. |
| publishDate |
2016 |
| dc.date.none.fl_str_mv |
2016 2020 2020 2020 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion |
| format |
article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/165158 |
| url |
https://hdl.handle.net/2445/165158 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Versió postprint del document publicat a: https://doi.org/10.1016/j.bmc.2016.09.037 Bioorganic & Medicinal Chemistry, 2016, vol. 24, num. 22, p. 5804-5815 https://doi.org/10.1016/j.bmc.2016.09.037 |
| dc.rights.none.fl_str_mv |
cc-by-nc-nd (c) Elsevier Ltd, 2016 http://creativecommons.org/licenses/by-nc-nd/3.0/es info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
cc-by-nc-nd (c) Elsevier Ltd, 2016 http://creativecommons.org/licenses/by-nc-nd/3.0/es |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
12 p. application/pdf |
| dc.publisher.none.fl_str_mv |
Elsevier Ltd |
| publisher.none.fl_str_mv |
Elsevier Ltd |
| dc.source.none.fl_str_mv |
Articles publicats en revistes (Química Inorgànica i Orgànica) reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| instname_str |
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| reponame_str |
Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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15,812429 |