Institute of Nutrition Josué de Castro, Federal University of Rio de Janeiro, Rio de Janeiro 21941-902, Brazil.
Institute of Medical Biochemistry Leopoldo de Meis, Federal University of Rio de Janeiro, Rio de Janeiro 21941-902, Brazil.
Biomed Pharmacother. 2024 Oct;179:117276. doi: 10.1016/j.biopha.2024.117276. Epub 2024 Aug 14.
Pharmacological properties of flavonoids have been reported, with an anticancer role amongst them, however, its mechanisms are not fully elucidated. In this study, the activity of quercetin and chrysin towards MCF-7 and MDA-MB-231 breast cancer cells was investigated. Cellular viability was determined after treatment with the compounds in different concentrations for 24 h. Secondly, cells were treated with fixed concentration of chrysin and different concentrations of quercetin with preincubation for 1 h. Both compounds inhibited cellular proliferation in dose-dependent manner. The association showed improvement in their cytotoxicity, more expressively with preincubation of quercetin. Quercetin and chrysin association induced cell cycle arrest in sub-G0/G1 phase in MDA-MB-231 cells, modified the expression of caspases-3 and -8,-8, inducing late apoptosis cell death. Taken together, our results demonstrate that both flavonoids inhibited cells growth in a dose-dependent manner and the association of quercetin improved chrysin's toxic effect over the cell lines.
黄酮类化合物的药理学特性已经被报道,其中包括抗癌作用,然而,其机制尚未完全阐明。在这项研究中,研究了槲皮素和白杨素对 MCF-7 和 MDA-MB-231 乳腺癌细胞的活性。用不同浓度的化合物处理细胞 24 小时后,测定细胞活力。其次,用固定浓度的白杨素和不同浓度的槲皮素处理细胞,并进行 1 小时的预孵育。这两种化合物均以剂量依赖性方式抑制细胞增殖。联合使用可提高其细胞毒性,槲皮素的预孵育效果更明显。槲皮素和白杨素联合使用可诱导 MDA-MB-231 细胞周期停滞在 sub-G0/G1 期,改变 caspase-3 和 -8 的表达,诱导晚期凋亡细胞死亡。综上所述,我们的研究结果表明,这两种黄酮类化合物均以剂量依赖性方式抑制细胞生长,槲皮素的联合使用可提高白杨素对细胞系的毒性作用。