Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies

Detalhes bibliográficos
Autor(a) principal: Silva, Débora E. S. [UNESP]
Data de Publicação: 2020
Outros Autores: Becceneri, Amanda B., Santiago, João V. B. [UNESP], Gomes Neto, José A. [UNESP], Ellena, Javier, Cominetti, Márcia R., Pereira, José C. M. [UNESP], Hannon, Michael J., Netto, Adelino V. G. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
DOI: 10.1039/d0dt01134g
Texto Completo: http://dx.doi.org/10.1039/d0dt01134g
http://hdl.handle.net/11449/206895
Resumo: Novel silver(i) complexes of the type [AgCl(PPh3)2(L)] {PPh3 = triphenylphosphine; L = VTSC = 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazone (1); VMTSC = 3-methoxy-4-[2-(morpholine-1-yl)ethoxy]benzaldehyde thiosemicarbazone (2); VPTSC = 3-methoxy-4-[2-(piperidine-1-yl)ethoxy]benzaldehyde thiosemicarbazone (3)} were synthesized and fully characterized by spectroscopic techniques. The molecular structures of complexes 2 and 3 were determined by single crystal X-ray diffraction. Compounds 1-3 exhibited appreciable cytotoxic activity against human tumor cells (lung A549, breast MDA-MB-231 and MCF-7) with IC50 values in 48 h of incubation ranging from 5.6 to 18 μM. Cellular uptake studies showed that complexes 1-3 were efficiently internalized after 3 hours of treatment in MDA-MB-231 cells. The effects of complex 1 on the cell morphology, cell cycle, induction of apoptosis, mitochondrial membrane potential (Δψm), and reactive oxygen species (ROS) production have been evaluated in triple negative breast cancer (TNBC) cells MDA-MB-231. Our results showed that complex 1 induced typical morphological alterations of cell death, an increase in cells at the sub-G1 phase, apoptosis, and mitochondrial membrane depolarization. Furthermore, DNA binding studies evidenced that 1 can bind to ct-DNA and does so without modifying the B-structure of the DNA, but that the binding is weak compared to that of Hoechst 33258.
id UNSP_9b7ecfde26d51fed57ce5b93b8b3030f
oai_identifier_str oai:repositorio.unesp.br:11449/206895
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studiesNovel silver(i) complexes of the type [AgCl(PPh3)2(L)] {PPh3 = triphenylphosphine; L = VTSC = 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazone (1); VMTSC = 3-methoxy-4-[2-(morpholine-1-yl)ethoxy]benzaldehyde thiosemicarbazone (2); VPTSC = 3-methoxy-4-[2-(piperidine-1-yl)ethoxy]benzaldehyde thiosemicarbazone (3)} were synthesized and fully characterized by spectroscopic techniques. The molecular structures of complexes 2 and 3 were determined by single crystal X-ray diffraction. Compounds 1-3 exhibited appreciable cytotoxic activity against human tumor cells (lung A549, breast MDA-MB-231 and MCF-7) with IC50 values in 48 h of incubation ranging from 5.6 to 18 μM. Cellular uptake studies showed that complexes 1-3 were efficiently internalized after 3 hours of treatment in MDA-MB-231 cells. The effects of complex 1 on the cell morphology, cell cycle, induction of apoptosis, mitochondrial membrane potential (Δψm), and reactive oxygen species (ROS) production have been evaluated in triple negative breast cancer (TNBC) cells MDA-MB-231. Our results showed that complex 1 induced typical morphological alterations of cell death, an increase in cells at the sub-G1 phase, apoptosis, and mitochondrial membrane depolarization. Furthermore, DNA binding studies evidenced that 1 can bind to ct-DNA and does so without modifying the B-structure of the DNA, but that the binding is weak compared to that of Hoechst 33258.Department of General and Inorganic Chemistry Department of Analytical Chemistry UNESP-São Paulo State University Institute of ChemistryDepartment de Gerontology Federal University of São CarlosSão Carlos Institute of Physics University of São PauloSchool of Chemistry University of BirminghamDepartment of General and Inorganic Chemistry Department of Analytical Chemistry UNESP-São Paulo State University Institute of ChemistryUniversidade Estadual Paulista (Unesp)Silva, Débora E. S. [UNESP]Becceneri, Amanda B.Santiago, João V. B. [UNESP]Gomes Neto, José A. [UNESP]Ellena, JavierCominetti, Márcia R.Pereira, José C. M. [UNESP]Hannon, Michael J.Netto, Adelino V. G. [UNESP]2021-06-25T10:45:33Z2021-06-25T10:45:33Z2020-12-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article16474-16487http://dx.doi.org/10.1039/d0dt01134gDalton Transactions, v. 49, n. 45, p. 16474-16487, 2020.1477-92341477-9226http://hdl.handle.net/11449/20689510.1039/d0dt01134g2-s2.0-85096885962Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDalton Transactionsinfo:eu-repo/semantics/openAccess2021-10-23T15:34:11Zoai:repositorio.unesp.br:11449/206895Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T13:44:27.623704Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
title Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
spellingShingle Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
Silva, Débora E. S. [UNESP]
Silva, Débora E. S. [UNESP]
title_short Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
title_full Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
title_fullStr Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
title_full_unstemmed Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
title_sort Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
author Silva, Débora E. S. [UNESP]
author_facet Silva, Débora E. S. [UNESP]
Silva, Débora E. S. [UNESP]
Becceneri, Amanda B.
Santiago, João V. B. [UNESP]
Gomes Neto, José A. [UNESP]
Ellena, Javier
Cominetti, Márcia R.
Pereira, José C. M. [UNESP]
Hannon, Michael J.
Netto, Adelino V. G. [UNESP]
Becceneri, Amanda B.
Santiago, João V. B. [UNESP]
Gomes Neto, José A. [UNESP]
Ellena, Javier
Cominetti, Márcia R.
Pereira, José C. M. [UNESP]
Hannon, Michael J.
Netto, Adelino V. G. [UNESP]
author_role author
author2 Becceneri, Amanda B.
Santiago, João V. B. [UNESP]
Gomes Neto, José A. [UNESP]
Ellena, Javier
Cominetti, Márcia R.
Pereira, José C. M. [UNESP]
Hannon, Michael J.
Netto, Adelino V. G. [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Silva, Débora E. S. [UNESP]
Becceneri, Amanda B.
Santiago, João V. B. [UNESP]
Gomes Neto, José A. [UNESP]
Ellena, Javier
Cominetti, Márcia R.
Pereira, José C. M. [UNESP]
Hannon, Michael J.
Netto, Adelino V. G. [UNESP]
description Novel silver(i) complexes of the type [AgCl(PPh3)2(L)] {PPh3 = triphenylphosphine; L = VTSC = 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazone (1); VMTSC = 3-methoxy-4-[2-(morpholine-1-yl)ethoxy]benzaldehyde thiosemicarbazone (2); VPTSC = 3-methoxy-4-[2-(piperidine-1-yl)ethoxy]benzaldehyde thiosemicarbazone (3)} were synthesized and fully characterized by spectroscopic techniques. The molecular structures of complexes 2 and 3 were determined by single crystal X-ray diffraction. Compounds 1-3 exhibited appreciable cytotoxic activity against human tumor cells (lung A549, breast MDA-MB-231 and MCF-7) with IC50 values in 48 h of incubation ranging from 5.6 to 18 μM. Cellular uptake studies showed that complexes 1-3 were efficiently internalized after 3 hours of treatment in MDA-MB-231 cells. The effects of complex 1 on the cell morphology, cell cycle, induction of apoptosis, mitochondrial membrane potential (Δψm), and reactive oxygen species (ROS) production have been evaluated in triple negative breast cancer (TNBC) cells MDA-MB-231. Our results showed that complex 1 induced typical morphological alterations of cell death, an increase in cells at the sub-G1 phase, apoptosis, and mitochondrial membrane depolarization. Furthermore, DNA binding studies evidenced that 1 can bind to ct-DNA and does so without modifying the B-structure of the DNA, but that the binding is weak compared to that of Hoechst 33258.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-07
2021-06-25T10:45:33Z
2021-06-25T10:45:33Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1039/d0dt01134g
Dalton Transactions, v. 49, n. 45, p. 16474-16487, 2020.
1477-9234
1477-9226
http://hdl.handle.net/11449/206895
10.1039/d0dt01134g
2-s2.0-85096885962
url http://dx.doi.org/10.1039/d0dt01134g
http://hdl.handle.net/11449/206895
identifier_str_mv Dalton Transactions, v. 49, n. 45, p. 16474-16487, 2020.
1477-9234
1477-9226
10.1039/d0dt01134g
2-s2.0-85096885962
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Dalton Transactions
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 16474-16487
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1822182433258209280
dc.identifier.doi.none.fl_str_mv 10.1039/d0dt01134g