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橙花叔醇,一种具有生物活性的化合物,通过细胞周期阻滞和诱导细胞凋亡抑制 HCT-116 结肠癌细胞的生长。

Nerolidol, Bioactive Compound Suppress Growth of HCT-116 Colorectal Cancer Cells Through Cell Cycle Arrest and Induction of Apoptosis.

机构信息

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.

出版信息

Appl Biochem Biotechnol. 2024 Mar;196(3):1365-1375. doi: 10.1007/s12010-023-04612-9. Epub 2023 Jul 3.

Abstract

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.

摘要

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。

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