Zhu Lijuan, Zhang Baolai, Luo Jianyun, Dong Shuhong, Zang Kaihong, Wu Yongjie
Department of Pharmacology, School of Basic Medical Science, Lanzhou University, Lanzhou, Gansu 730000, P.R. China.
Department of Pharmacology, College of Pharmacy, Gansu University of Traditional Chinese Medicine, Lanzhou, Gansu 730000, P.R. China.
Oncol Lett. 2019 Jul;18(1):189-196. doi: 10.3892/ol.2019.10288. Epub 2019 Apr 30.
Previous studies have demonstrated that ampelopsin (AMP), a type of flavonoid isolated from the stems and leaves of , exhibits anti-cancer activity in various types of cancer. Conversion of AMP into its sodium salt (AMP-Na) conferred enhanced solubility and stability to it. The present study aimed to evaluate the anti-cancer activity of AMP-Na in human lung adenocarcinoma cell lines and to investigate its mechanisms of action. Cell proliferation and viability were assessed by MTT and colony formation assays, and cell migration was determined using a scratch wound healing assay. The cell cycle distribution, apoptosis rate and tubulin immunofluorescence intensity were analyzed using flow cytometry, the cell ultra-microstructure was examined using transmission electron microscopy and the accumulation of tubulin was determined using laser confocal microscopy. The results demonstrated that AMP-Na significantly inhibited the proliferation, clonogenicity and migration of human lung adenocarcinoma cells. Furthermore, AMP-Na induced SPC-A-1 cell apoptosis, and promoted tubulin polymerization. The results suggested that the underlying mechanisms of AMP-Na may involve targeting of microtubules and tubulin polymerization to subsequently disrupt mitosis and induce cell cycle arrest at the S-phase.
先前的研究表明,从[植物名称]的茎和叶中分离出的一种黄酮类化合物——蛇葡萄素(AMP),在多种癌症中均表现出抗癌活性。将AMP转化为其钠盐(AMP-Na)可增强其溶解度和稳定性。本研究旨在评估AMP-Na对人肺腺癌细胞系的抗癌活性,并探讨其作用机制。通过MTT法和集落形成试验评估细胞增殖和活力,使用划痕伤口愈合试验测定细胞迁移。采用流式细胞术分析细胞周期分布、凋亡率和微管蛋白免疫荧光强度,使用透射电子显微镜检查细胞超微结构,使用激光共聚焦显微镜测定微管蛋白的积累。结果表明,AMP-Na显著抑制人肺腺癌细胞的增殖、克隆形成能力和迁移。此外,AMP-Na诱导SPC-A-1细胞凋亡,并促进微管蛋白聚合。结果提示,AMP-Na的潜在作用机制可能涉及靶向微管和微管蛋白聚合,随后破坏有丝分裂并诱导细胞周期停滞于S期。