Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells

ABSTRACT: A series of resveratrol/hydrazone hybrids were obtained and elucidated by spectroscopic analysis. All compounds were evaluated against colorectal cancer cells (SW480 and Sw620) and nonmalignant cell lines (HaCaT and CHO-K1) to establish the selectivity index. Among the hybrids evaluated, c...

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Autores:
Castrillón López, Wilson Andrés
Herrera Ramírez, Angie
Moreno Quintero, Gustavo Alberto
Coa Acuña, Juan Carlos
Cardona Galeano, Wilson
Tonny Williams, Naranjo Preciado
Tipo de recurso:
Article of investigation
Fecha de publicación:
2022
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/41405
Acceso en línea:
https://hdl.handle.net/10495/41405
Palabra clave:
Neoplasias Colorrectales
Colorectal Neoplasms
Resveratrol
Hydrazones
Hidrazonas
Apoptosis
https://id.nlm.nih.gov/mesh/D015179
https://id.nlm.nih.gov/mesh/D000077185
https://id.nlm.nih.gov/mesh/D006835
https://id.nlm.nih.gov/mesh/D017209
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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dc.title.spa.fl_str_mv Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
title Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
spellingShingle Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
Neoplasias Colorrectales
Colorectal Neoplasms
Resveratrol
Hydrazones
Hidrazonas
Apoptosis
https://id.nlm.nih.gov/mesh/D015179
https://id.nlm.nih.gov/mesh/D000077185
https://id.nlm.nih.gov/mesh/D006835
https://id.nlm.nih.gov/mesh/D017209
title_short Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
title_full Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
title_fullStr Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
title_full_unstemmed Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
title_sort Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells
dc.creator.fl_str_mv Castrillón López, Wilson Andrés
Herrera Ramírez, Angie
Moreno Quintero, Gustavo Alberto
Coa Acuña, Juan Carlos
Cardona Galeano, Wilson
Tonny Williams, Naranjo Preciado
dc.contributor.author.none.fl_str_mv Castrillón López, Wilson Andrés
Herrera Ramírez, Angie
Moreno Quintero, Gustavo Alberto
Coa Acuña, Juan Carlos
Cardona Galeano, Wilson
Tonny Williams, Naranjo Preciado
dc.contributor.researchgroup.spa.fl_str_mv Micología Médica y Experimental
Química de Plantas Colombianas
dc.subject.decs.none.fl_str_mv Neoplasias Colorrectales
Colorectal Neoplasms
Resveratrol
Hydrazones
Hidrazonas
Apoptosis
topic Neoplasias Colorrectales
Colorectal Neoplasms
Resveratrol
Hydrazones
Hidrazonas
Apoptosis
https://id.nlm.nih.gov/mesh/D015179
https://id.nlm.nih.gov/mesh/D000077185
https://id.nlm.nih.gov/mesh/D006835
https://id.nlm.nih.gov/mesh/D017209
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D015179
https://id.nlm.nih.gov/mesh/D000077185
https://id.nlm.nih.gov/mesh/D006835
https://id.nlm.nih.gov/mesh/D017209
description ABSTRACT: A series of resveratrol/hydrazone hybrids were obtained and elucidated by spectroscopic analysis. All compounds were evaluated against colorectal cancer cells (SW480 and Sw620) and nonmalignant cell lines (HaCaT and CHO-K1) to establish the selectivity index. Among the hybrids evaluated, compounds 6e and 7 displayed the highest cytotoxic activity with IC50 values of = 6.5 ± 1.9 µM and 19.0 ± 1.4 µM, respectively, on SW480 cells. In addition, hybrid 7 also exhibited activity on SW620 cells with an IC50 value of 38.41 ± 3.3 µM. Both compounds were even more toxic against these malignant cells in comparison to the nonmalignant ones, as evidenced by higher selectivity indices 48 h after treatment. These compounds displayed better activity and selectivity than parental compounds (PIH and Resveratrol) and the reference drug (5-FU). In addition, it was observed that both compounds caused antiproliferative activity probably exerted by cell cycle arrest at the G2/M or G0/G1 phases, with the formation of cells in the subG0/G1 phase. Furthermore, it was noticed that compound 7 induced mitochondrial depolarization in SW480 cells and positive staining for propidium iodide in both cancer cell lines, suggesting cell membrane damage involving either apoptosis or other processes of death.
publishDate 2022
dc.date.issued.none.fl_str_mv 2022
dc.date.accessioned.none.fl_str_mv 2024-08-25T14:08:46Z
dc.date.available.none.fl_str_mv 2024-08-25T14:08:46Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Castrillón-López W, Herrera-Ramírez A, Moreno-Quintero G, Coa JC, Naranjo TW, Cardona-Galeano W. Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells. Pharmaceutics. 2022 Oct 24;14(11):2278. doi: 10.3390/pharmaceutics14112278.
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/41405
dc.identifier.doi.none.fl_str_mv 10.3390/ pharmaceutics14112278
dc.identifier.eissn.none.fl_str_mv 1999-4923
identifier_str_mv Castrillón-López W, Herrera-Ramírez A, Moreno-Quintero G, Coa JC, Naranjo TW, Cardona-Galeano W. Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells. Pharmaceutics. 2022 Oct 24;14(11):2278. doi: 10.3390/pharmaceutics14112278.
10.3390/ pharmaceutics14112278
1999-4923
url https://hdl.handle.net/10495/41405
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Pharmaceutics
dc.relation.citationendpage.spa.fl_str_mv 20
dc.relation.citationissue.spa.fl_str_mv 11
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 14
dc.relation.ispartofjournal.spa.fl_str_mv Pharmaceutics
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dc.publisher.place.spa.fl_str_mv Basilea, Suiza
institution Universidad de Antioquia
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spelling Castrillón López, Wilson AndrésHerrera Ramírez, AngieMoreno Quintero, Gustavo AlbertoCoa Acuña, Juan CarlosCardona Galeano, WilsonTonny Williams, Naranjo PreciadoMicología Médica y ExperimentalQuímica de Plantas Colombianas2024-08-25T14:08:46Z2024-08-25T14:08:46Z2022Castrillón-López W, Herrera-Ramírez A, Moreno-Quintero G, Coa JC, Naranjo TW, Cardona-Galeano W. Resveratrol/Hydrazone Hybrids: Synthesis and Chemopreventive Activity against Colorectal Cancer Cells. Pharmaceutics. 2022 Oct 24;14(11):2278. doi: 10.3390/pharmaceutics14112278.https://hdl.handle.net/10495/4140510.3390/ pharmaceutics141122781999-4923ABSTRACT: A series of resveratrol/hydrazone hybrids were obtained and elucidated by spectroscopic analysis. All compounds were evaluated against colorectal cancer cells (SW480 and Sw620) and nonmalignant cell lines (HaCaT and CHO-K1) to establish the selectivity index. Among the hybrids evaluated, compounds 6e and 7 displayed the highest cytotoxic activity with IC50 values of = 6.5 ± 1.9 µM and 19.0 ± 1.4 µM, respectively, on SW480 cells. In addition, hybrid 7 also exhibited activity on SW620 cells with an IC50 value of 38.41 ± 3.3 µM. Both compounds were even more toxic against these malignant cells in comparison to the nonmalignant ones, as evidenced by higher selectivity indices 48 h after treatment. These compounds displayed better activity and selectivity than parental compounds (PIH and Resveratrol) and the reference drug (5-FU). In addition, it was observed that both compounds caused antiproliferative activity probably exerted by cell cycle arrest at the G2/M or G0/G1 phases, with the formation of cells in the subG0/G1 phase. Furthermore, it was noticed that compound 7 induced mitochondrial depolarization in SW480 cells and positive staining for propidium iodide in both cancer cell lines, suggesting cell membrane damage involving either apoptosis or other processes of death.Colombia. Ministerio de Ciencia, Tecnología e Innovación - MincienciasColombia. Ministerio de Educación Nacional - MineducaciónColombia. 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