Karpagam College of Pharmacy, Coimbatore, Tamil Nadu, India.
Asian Pac J Cancer Prev. 2022 Nov 1;23(11):3657-3663. doi: 10.31557/APJCP.2022.23.11.3657.
The medicinal plant Ipomoea aquatica belonging to convulvulaceae family is an effective natural herb for treatment of various ailments and possesses effective anticancer activity. The aim of the work is to characterize a secondary metabolite merromoside (a resin glycoside) for anti-breast cancer activity through down regulation of ROS species.
The Extract of the whole plant has been prepared by maceration method using 50%v/v ethanol in distilled water to get a hydroalcoholic extract. The phytochemical evaluation reveals that the active secondary metabolite was isolated by using column chromatographic technique. The isolated compound was evaluated for its anticancer properties through invitro method such as 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay on Michigan Cancer Foundation-7 Cell lines. The purity and structural characterization were done by high-performance thin layer chromatography, Fourier Transform Infrared Spectroscopy, Proton and13C Nuclear Magnetic Resonance spectroscopy and Liquid Chromatography-Mass Spectrometry.
The isolated compound (W04) from the derived extract showed Rf value of 0.79 that showed IC50 of 182.8μg/ml. The chemical structure of W04 has been confirmed as [4,5-dihydroxy-6-[5-hydroxy-2-methyl-4-(2-methylpropanoyloxy)-6-[(24,25,26-trihydroxy-5,23-dimethyl-9-oxo-19-pentyl-2,4,8,20,22-pentaoxatricyclo[19.2.2.13,7]hexacosan-6-yl)oxy]oxan-3-yl]oxy-2-methyloxan-3-yl] 2-methyl propanoate with the molecular weight of 979.15268. The isolated compound merromoside from hydroalcoholic extract of Ipomoea aquatica has been evaluated for anti-breast cancer properties. The down regulation of ROS species will prevent reverse signalling and angiogenesis. This indicates that merromoside will overcome MDR in breast cancer especially DOX-resistant.
旋花科植物空心菜是一种有效的天然草药,可用于治疗各种疾病,并具有有效的抗癌活性。本工作的目的是通过下调 ROS 种类来表征次生代谢物 Merromoside(树脂糖苷)的抗乳腺癌活性。
采用 50%v/v 乙醇在蒸馏水中的浸渍法从全植物提取物中制备水醇提取物。植物化学评价表明,采用柱色谱技术分离出活性次生代谢物。通过体外方法,如密歇根癌症基金会-7 细胞系的 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐测定法,评估分离得到的化合物的抗癌特性。通过高效薄层色谱、傅里叶变换红外光谱、质子和 13C 核磁共振光谱以及液相色谱-质谱对其纯度和结构进行了表征。
从衍生提取物中分离得到的化合物(W04)显示出 Rf 值为 0.79,IC50 为 182.8μg/ml。W04 的化学结构已被确认为 [4,5-二羟基-6-[5-羟基-2-甲基-4-(2-甲基丙酰氧基)-6-[(24,25,26-三羟基-5,23-二甲基-9-氧代-19-戊基-2,4,8,20,22-五氧杂三环[19.2.2.13,7]十六烷-6-基)氧基]氧杂环戊烷-3-基]氧基-2-甲基氧杂环戊烷-3-基]2-甲基丙酸盐,分子量为 979.15268。从空心菜水醇提取物中分离得到的次生代谢物 Merromoside 已被评估其抗乳腺癌特性。ROS 种类的下调将阻止反向信号和血管生成。这表明 Merromoside 将克服乳腺癌中的多药耐药性,特别是 DOX 耐药性。