Silver(i) complexes of 3-methoxy-4-hydroxybenzaldehyde thiosemicarbazones and triphenylphosphine: structural, cytotoxicity, and apoptotic studies
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , |
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. |
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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 |