School of Public Health, Bengbu Medical College, Bengbu, 233030, People's Republic of China.
School of Life Science, Anhui Province Key Laboratory of Translational Cancer Research, Bengbu Medical College, Bengbu, 233030, People's Republic of China.
Sci Rep. 2021 Jan 28;11(1):2504. doi: 10.1038/s41598-021-81815-2.
Sulforaphane (SFN) extracted from broccoli sprout has previously been investigated for its potential properties in cancers, however, the underlying mechanisms of the anticancer activity of SFN remain not fully understood. In the present study, we investigate the effects of SFN on cell proliferation, cell cycle, cell apoptosis, and also the expression of several cell cycle and apoptosis-related genes by MTT assay, flow cytometry and western blot analysis in gastric cancer (GC) cells. The results showed that SFN could impair the colony-forming ability in BGC-823 and MGC-803 cell lines compared with the control. In addition, SFN significantly suppressed cell proliferation by arresting the cell cycle at the S phase and enhancing cell apoptosis in GC cells in a dose-dependent manner. Western blot results showed that SFN treatment significantly increased the expression levels of p53, p21 and decreased CDK2 expression, which directly regulated the S phase transition. The Bax and cleaved-caspase-3 genes involved in apoptosis executive functions were significantly increased in a dose-dependent manner in BGC-823 and MGC-803 cells. These results suggested that SFN-induced S phase cell cycle arrest and apoptosis through p53-dependent manner in GC cells, which suggested that SFN has a potential therapeutic application in the treatment and prevention of GC.
从西兰花芽中提取的萝卜硫素 (SFN) 先前因其在癌症中的潜在特性而受到研究,然而,SFN 的抗癌活性的潜在机制仍不完全清楚。在本研究中,我们通过 MTT 检测、流式细胞术和 Western blot 分析研究了 SFN 对胃癌 (GC) 细胞增殖、细胞周期、细胞凋亡以及几种细胞周期和凋亡相关基因表达的影响。结果表明,与对照组相比,SFN 可削弱 BGC-823 和 MGC-803 细胞系中的集落形成能力。此外,SFN 以剂量依赖性方式通过将细胞周期阻滞在 S 期和增强 GC 细胞凋亡来显著抑制细胞增殖。Western blot 结果表明,SFN 处理显著增加了 p53、p21 的表达水平,并降低了 CDK2 的表达,这直接调节了 S 期转变。Bax 和 cleaved-caspase-3 基因参与凋亡执行功能,在 BGC-823 和 MGC-803 细胞中呈剂量依赖性显著增加。这些结果表明,SFN 通过 p53 依赖性途径诱导 GC 细胞中的 S 期细胞周期阻滞和凋亡,表明 SFN 在 GC 的治疗和预防中有潜在的治疗应用。