Nuclear Medicine Department, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250021, China.
Department of Botany and Microbiology, College of Science, King Saud University, PO Box -2455, Riyadh, 11451, Saudi Arabia.
Appl Biochem Biotechnol. 2024 Mar;196(3):1365-1375. doi: 10.1007/s12010-023-04612-9. Epub 2023 Jul 3.
Colon cancer is the most prevalent cancer and causes the highest cancer-associated mortality in both men and women globally. It has a high incidence and fatality rate, which places a significant burden on the healthcare system. The current work was performed to understand the beneficial roles of nerolidol on the viability and cytotoxic mechanisms in the colon cancer HCT-116 cells. The MTT cytotoxicity assay was done to investigate the effect of nerolidol at different doses (5-100 µM) on the HCT-116 cell viability. The impacts of nerolidol on ROS accumulation and apoptosis were investigated using DCFH-DA, DAPI, and dual staining assays, respectively. The flow cytometry analysis was performed to study the influence of nerolidol on the cell cycle arrest in the HCT-116 cells. The outcomes of the MTT assay demonstrated that nerolidol at different doses (5-100 µM) substantially inhibited the HCT-116 cell viability with an IC50 level of 25 µM. The treatment with nerolidol appreciably boosted the ROS level in the HCT-116 cells. The findings of DAPI and dual staining revealed higher apoptotic incidences in the nerolidol-exposed HCT-116 cells, which supports its ability to stimulate apoptosis. The flow cytometry analysis demonstrated the considerable inhibition in cell cycle at the G0/G1 phase in the nerolidol-exposed HCT-116 cells. Our research showed that nerolidol can inhibit the cell cycle, increase ROS accumulation, and activate apoptosis in HCT-116 cells. In light of this, it may prove to be a potent and salutary candidate to treat colon cancer.
结肠癌是全球男性和女性中最常见的癌症,也是导致癌症相关死亡率最高的癌症。它的发病率和死亡率都很高,这给医疗系统带来了巨大的负担。目前的工作是为了了解橙花叔醇对结肠癌 HCT-116 细胞活力和细胞毒性机制的有益作用。通过 MTT 细胞毒性测定法来研究橙花叔醇在不同剂量(5-100 μM)下对 HCT-116 细胞活力的影响。使用 DCFH-DA、DAPI 和双重染色测定法分别研究橙花叔醇对 ROS 积累和细胞凋亡的影响。通过流式细胞术分析来研究橙花叔醇对 HCT-116 细胞周期停滞的影响。MTT 测定法的结果表明,橙花叔醇在不同剂量(5-100 μM)下可显著抑制 HCT-116 细胞活力,IC50 值为 25 μM。橙花叔醇处理可显著增加 HCT-116 细胞中的 ROS 水平。DAPI 和双重染色的结果显示,橙花叔醇暴露的 HCT-116 细胞中的凋亡发生率更高,这支持了它刺激凋亡的能力。流式细胞术分析表明,橙花叔醇暴露的 HCT-116 细胞中的细胞周期在 G0/G1 期受到显著抑制。我们的研究表明,橙花叔醇可以抑制细胞周期,增加 ROS 积累,并激活 HCT-116 细胞中的细胞凋亡。因此,它可能被证明是一种治疗结肠癌的有效候选药物。