褐毛鼠和chamaethamus的随机抗癌和细胞毒活性。

Florence Dushimemaria, C Iwanette Du Preez, Davis R Mumbengegwi
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引用次数: 10

摘要

背景:植物一直被证明是一种可靠的药物来源,但尚未得到充分的探索。鉴于此,人们不断需要新的癌症治疗方案。纳米比亚的植物种类丰富多样,超过4300种,其中17%是纳米比亚特有的。生长在纳米比亚不同气候带的植物产生许多次生代谢物,作为适应环境的一部分。本文重点介绍了这些植物化学物质的筛选及其体外细胞毒和抗癌特性。为此,我们随机选择了两种纳米比亚植物:chamaethamnus和Guibourtia coleosperma。材料与方法:采用薄层色谱法筛选香豆素类、生物碱类、黄酮类、蒽醌类、甾体类和萜类化合物。抗癌筛选是在三种癌细胞系上进行的,而细胞毒性是用人成纤维细胞系测定的,两者都使用SRB方法。结果:两种植物的有机提取物和水提液中均检测到生物碱、蒽醌类、黄酮类和甾类化合物。有机植物提取物对肿瘤细胞株的抗增殖作用优于水提物;chamaethamnus有机根提取物对TK10、UACC62和MCF7细胞的IC50分别为16.08、29.12和24.67µg/mL。此外,细胞毒性分析显示,除chamaethamnus有机根提取物显示出显著的细胞毒性(IC50为13.03µg/mL)外,其他提取物均无毒。结论:沙鼠属植物是开发基于植物的癌症治疗药物的潜在候选者。该研究显示了随机筛选在植物药物发现中与其民族医学用途无关的药理活性的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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RANDOMIZED ANTICANCER AND CYTOTOXICITY ACTIVITIES OF GUIBOURTIA COLEOSPERMA AND DIOSPYROS CHAMAETHAMNUS.

Background: Plants have consistently proven to be a reliable and yet not fully explored source of medicines. In light of this, there is a constant demand for new treatment regimens for cancer. Namibia has a rich diversity of plant species of over 4300 with 17 % of them being endemic to Namibia. Plants growing in Namibia's diverse climatic zones produce many secondary metabolites as part of adaptation to their environment. This article focused on the screening of such phytochemicals and their cytotoxic and anticancer properties in vitro. Two Namibian plants Diospyros chamaethamnus and Guibourtia coleosperma were randomly selected for this purpose.

Materials and methods: The plants were screened for the presence of coumarins, alkaloids, flavonoids, anthraquinones, steroids and terpenoids using thin layer chromatography. Anticancer screening was performed on a panel of three cancer cell lines, while cytotoxicity was determined using a human fibroblast cell line, both using the SRB method.

Results: Alkaloids, anthraquinones, flavonoids and steroids were detected in both organic and aqueous extracts of the two plants. The organic plant extracts had a greater anti-proliferative effect on the cancer cell lines than the aqueous extracts; the D. chamaethamnus organic root extract was the most potent with an IC50 of 16.08, 29.12 and 24.67 µg/mL against TK10, UACC62 and MCF7 cells, respectively. Furthermore, cytotoxicity analysis revealed the non-toxic nature of the extracts, except for the organic root extract of D. chamaethamnus that showed significant cytotoxicity (IC50 13.03 µg/mL).

Conclusion: D. chamaethamnus is a potential candidate for the development of a plant based cancer treatment. The study showed the value of random screening in drug discovery from plants for pharmacological activity that is unrelated to their ethnomedicinal uses.

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