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...
- 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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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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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 |
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eng |
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eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Pharmaceutics |
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20 |
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11 |
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1 |
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14 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Pharmaceutics |
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http://creativecommons.org/licenses/by/2.5/co/ |
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openAccess |
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20 páginas |
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MDPI |
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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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