Jayaprakasha G K, Mandadi K K, Poulose Shibu M, Jadegoud Y, Nagana Gowda G A, Patil Bhimanagouda S
Vegetable & Fruit Improvement Center, Department of Horticultural Sciences, Texas A&M University, College Station, TX 77843-2119, USA.
Bioorg Med Chem. 2007 Jul 15;15(14):4923-32. doi: 10.1016/j.bmc.2007.04.044. Epub 2007 Apr 30.
Recently several plant derived natural compounds have been screened for their anticancer activity in order to identify putative compounds with novel structures or mechanism of action. In the present study, fruits of Poncirus trifoliata were extracted with acetone and loaded onto silica gel column chromatography. The column was eluted with different solvents to obtain two bioactive compounds. The purity of compounds was analyzed by HPLC and their structures were identified by 1H and 13C NMR experiments as beta-sitosterol and 2-hydroxy-1,2,3-propanetricarboxylic acid 2-methyl ester (HPCME). beta-Sitosterol, HPCME, and trolox were tested for their antioxidant capacity by oxygen radical absorbance capacity (ORAC) measurement. Further, these compounds were tested for their inhibition of cancer cell proliferation and apoptosis using human colon cancer cell line (HT-29). These results were compared with the corresponding activity on non-cancerous (COS-1 fibroblast) cells. Cell proliferation and induction of apoptosis were determined by MTT assay and nuclear staining. The MTT assay indicated that both the compounds exhibited differential inhibition at various concentrations. Significant arrest of cell growth was observed with beta-sitosterol even at low concentration such as 0.63 microM in 48 h and none of the compounds exerted any apparent cytostatic effects on the non-cancerous COS-1 fibroblast cells. Growth inhibition assay suggested the potential use of bioactive compounds as cancer chemopreventive and therapeutic agents. This is the first report on HPCME isolation and identification from Rutaceae family and beta-sitosterol from P. trifoliata.
最近,人们对几种植物来源的天然化合物进行了抗癌活性筛选,以确定具有新结构或作用机制的潜在化合物。在本研究中,用丙酮提取了枳壳果实,并将其加载到硅胶柱色谱上。用不同溶剂洗脱柱子以获得两种生物活性化合物。通过高效液相色谱分析化合物的纯度,并通过1H和13C核磁共振实验确定其结构为β-谷甾醇和2-羟基-1,2,3-丙烷三羧酸2-甲酯(HPCME)。通过氧自由基吸收能力(ORAC)测量来测试β-谷甾醇、HPCME和生育三烯酚的抗氧化能力。此外,使用人结肠癌细胞系(HT-29)测试了这些化合物对癌细胞增殖和凋亡的抑制作用。将这些结果与对非癌细胞(COS-1成纤维细胞)的相应活性进行比较。通过MTT法和核染色来确定细胞增殖和凋亡诱导情况。MTT法表明,这两种化合物在不同浓度下均表现出不同程度的抑制作用。即使在低浓度如0.63 microM下,48小时内β-谷甾醇也能显著抑制细胞生长,并且没有一种化合物对非癌性COS-1成纤维细胞产生明显的细胞抑制作用。生长抑制试验表明,这些生物活性化合物具有作为癌症化学预防和治疗剂的潜在用途。这是首次从芸香科中分离鉴定出HPCME以及从枳壳中分离鉴定出β-谷甾醇的报告。