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Dithiobiureas Palladium(II) complexes' studies: From their synthesis to their biological action.
Herrero, Jorge M; Fabra, David; Matesanz, Ana I; Hernández, Carolina; Sánchez-Pérez, Isabel; Quiroga, Adoracion G.
Afiliação
  • Herrero JM; Departamento de Bioquímica, Facultad de Medicina and Instituto de Investigaciones Biomédicas Albert Sols, Universidad Autónoma de Madrid, 28029 Madrid, Spain; Cancer Stem Cell and Fibroinflammatory Microenvironment Group, Chronic Diseases and Cancer Area 3 -Instituto Ramón y Cajal de Investigación S
  • Fabra D; Departamento de Química Inorgánica, Facultad de Ciencias and IadChem, Calle Francisco Tomas y Valiente 7, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
  • Matesanz AI; Departamento de Química Inorgánica, Facultad de Ciencias and IadChem, Calle Francisco Tomas y Valiente 7, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
  • Hernández C; Departamento de Química Inorgánica, Orgánica y Bioquímica, Facultad de Ciencias del Medio Ambiente, Avd. Carlos III s/n, Universidad de Castilla-La Mancha, 45071 Toledo, Spain.
  • Sánchez-Pérez I; Departamento de Bioquímica, Facultad de Medicina and Instituto de Investigaciones Biomédicas Albert Sols, Universidad Autónoma de Madrid, 28029 Madrid, Spain; Cancer Stem Cell and Fibroinflammatory Microenvironment Group, Chronic Diseases and Cancer Area 3 -Instituto Ramón y Cajal de Investigación S
  • Quiroga AG; Departamento de Química Inorgánica, Facultad de Ciencias and IadChem, Calle Francisco Tomas y Valiente 7, Universidad Autónoma de Madrid, 28049 Madrid, Spain. Electronic address: adoracion.gomez@uam.es.
J Inorg Biochem ; 246: 112261, 2023 09.
Article em En | MEDLINE | ID: mdl-37271620
ABSTRACT
Dithiobiureas coordination chemistry towards palladium (II) ions and their possible application is presented and discussed. 1,6-(4-Methoxyphenyl)-2,5-dithiobiurea and 1,6-(4-chlorophenyl)-2,5-dithiobiurea afford two Pd(II) complexes with the general formula [Pd2(H2L)Cl2(PPh3)2]. The metal ion forms one chelate ring with the dithiobiurea, and binds to a triphenylphosphine and an additional leaving group cisplatin like. One of the complexes (1) is endowed not only with stability in DMSO and aqua solutions containing a biological buffer but also with cytotoxicity versus gastric cancer cell lines. Complex 1 does not interact covalently to DNA models, neither activates p53 or Checkpoint Kinase 1 key proteins for DNA damage response. Thus, we propose that complex 1 exerts its action by activating Mitogen-Activated Protein Kinases [p38, Extracellular signal-regulated kinases (ERKs), c-Jun N-terminal kinases (JNKs)] as cell death inductors.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paládio / Transdução de Sinais Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paládio / Transdução de Sinais Idioma: En Ano de publicação: 2023 Tipo de documento: Article