Taiwo Bamigboye J, Fatokun Amos A, Olubiyi Olujide O, Bamigboye-Taiwo Olukemi T, van Heerden Fanie R, Wright Colin W
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Obafemi Awolowo University, Ile Ife, Nigeria; School of Pharmacy, Faculty of Life Sciences, University of Bradford, Bradford BD7 1DP, England, United Kingdom.
School of Pharmacy, Faculty of Life Sciences, University of Bradford, Bradford BD7 1DP, England, United Kingdom.
Bioorg Med Chem. 2017 Apr 15;25(8):2327-2335. doi: 10.1016/j.bmc.2017.02.040. Epub 2017 Feb 22.
Cancer is now the second-leading cause of mortality and morbidity, behind only heart disease, necessitating urgent development of (chemo)therapeutic interventions to stem the growing burden of cancer cases and cancer death. Plants represent a credible source of promising drug leads in this regard, with a long history of proven use in the indigenous treatment of cancer. This study therefore investigated Anacardium occidentale, one of the plants in a Nigerian Traditional Medicine formulation commonly used to manage cancerous diseases, for cytotoxic activity. Bioassay-guided fractionation, spectroscopy, Alamar blue fluorescence-based viability assay in cultured HeLa cells and microscopy were used. Four compounds, zoapatanolide A (1), agathisflavone (2), 1,2-bis(2,6-dimethoxy-4-methoxycarbonylphenyl)ethane (anacardicin, 3) and methyl gallate (4), were isolated, with the most potent being zoapatanolide A with an IC value of 36.2±9.8µM in the viability assay. To gain an insight into the likely molecular basis of their observed cytotoxic effects, Autodock Vina binding free energies of each of the isolated compounds with seven molecular targets implicated in cancer development (MAPK8, MAPK10, MAP3K12, MAPK3, MAPK1, MAPK7 and VEGF), were calculated. Pearson correlation coefficients were obtained with experimentally-determined IC in the Alamar blue viability assay. While these compounds were not as potent as a standard anticancer compound, doxorubicin, the results provide reasonable evidence that the plant species contains compounds with cytotoxic activity. This study provides some evidence of why this plant is used ethnobotanically in anticancer herbal formulations and justifies investigating Nigerian medicinal plants highlighted in recent ethnobotanical surveys.
癌症如今是仅次于心脏病的第二大致死和发病原因,因此迫切需要开发(化学)治疗干预措施,以遏制癌症病例和癌症死亡日益增长的负担。在这方面,植物是有前景的药物先导物的可靠来源,在本土癌症治疗中有着长期的应用历史。因此,本研究调查了腰果,它是尼日利亚传统医学配方中常用于治疗癌症疾病的植物之一,以检测其细胞毒性活性。采用了生物测定引导的分级分离、光谱学、基于阿拉玛蓝荧光的培养HeLa细胞活力测定和显微镜检查。分离出了四种化合物,即佐帕他诺内酯A(1)、贝壳杉黄酮(2)、1,2 - 双(2,6 - 二甲氧基 - 4 - 甲氧基羰基苯基)乙烷(漆树素,3)和没食子酸甲酯(4),其中最具活性的是佐帕他诺内酯A,在活力测定中的IC值为36.2±9.8µM。为了深入了解其观察到的细胞毒性作用的可能分子基础,计算了每种分离化合物与七个与癌症发展相关的分子靶点(MAPK8、MAPK10、MAP3K12、MAPK3、MAPK1、MAPK7和VEGF)的Autodock Vina结合自由能。通过阿拉玛蓝活力测定实验确定的IC值获得了皮尔逊相关系数。虽然这些化合物不如标准抗癌化合物阿霉素有效,但结果提供了合理证据,表明该植物物种含有具有细胞毒性活性的化合物。本研究为该植物在抗癌草药配方中的民族植物学应用提供了一些证据,并证明了对近期民族植物学调查中突出的尼日利亚药用植物进行研究的合理性。