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

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 6...

Full description

Saved in:
Bibliographic Details
Published in:Pharmaceutics 2022-10, Vol.14 (11), p.2278
Main Authors: Castrillón-López, Wilson, Herrera-Ramírez, Angie, Moreno-Quintero, Gustavo, Coa, Juan Carlos, Naranjo, Tonny W, Cardona-Galeano, Wilson
Format: Article
Language:English
Subjects:
antiproliferative activity
Apoptosis
Cancer therapies
Care and treatment
Cell cycle
Cell division
Chemoprevention
Chemotherapy
Chromatography
Colorectal cancer
cytotoxicity
Diagnosis
Dosage and administration
hybrid compounds
hydrazone
Patient outcomes
Resveratrol
Signal transduction
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary: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.
ISSN:1999-4923
1999-4923
DOI:10.3390/pharmaceutics14112278