Lamula Siphamandla Qhubekani Njabuliso, Bhanisa Thando, Wium Martha, Paccez Juliano Domiraci, Zerbini Luiz Fernando, Buwa-Komoreng Lisa V
Infectious Diseases and Medicinal Plants, Botany Department, Faculty of Science and Agriculture, University of Fort Hare, Private Bag X1314, Alice 5700, South Africa.
International Centre for Genetic Engineering and Biotechnology (ICGEB), Weirner & Beit Building, Anzio Rd, Observatory, Cape Town 7935, South Africa.
Int J Mol Sci. 2025 Aug 6;26(15):7623. doi: 10.3390/ijms26157623.
Despite the significant advancements in treatment and prevention, the fight against cancer is ongoing worldwide. This study evaluated the pharmacological properties and anticancer activity of bark, traditionally used by the indigenous communities of KwaZulu Natal and Eastern Cape Provinces of South Africa to treat cancer and related illnesses. Phytochemical screening, high-performance liquid chromatography-diode array detection (HPLC-DAD), and Fourier-transform infrared spectroscopy (FTIR) analyses were carried out using established protocols. The antioxidant activity was assessed via the 2,2-diphenyl-1-picrylhydrazyl (DPPH) scavenging capacity and nitric oxide radicals. The anticancer activity was evaluated using the MTT assay (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). Phytochemical analysis revealed the presence of saponins, flavonoids, terpenoids, alkaloids, steroids, cardiac glycosides, and phlobatannins. The HPLC-DAD analysis detected seven distinctive peaks in the aqueous extract and three distinctive peaks in the methanolic extract. The FTIR spectra of the aqueous extract displayed characteristic peaks corresponding to O-H, C=O, C=C, and =C-H functional groups. Among the tested extracts, the methanol extract exhibited the strongest antioxidant activity, followed by the ethanolic extract, in both DPPH and nitric oxide. The methanol extract showed a higher cell proliferation inhibition against the DU-145 cancer cell line with the percentage of inhibition of 37.8%, followed by the aqueous extract with 36.3%. In contrast, limited activity was observed against PC-3, SK-UT-1, and AGS cell lines. The results demonstrated notable dose-dependent antioxidant and antiproliferative activities supporting the ethnomedicinal use of bark in cancer management. These findings warrant further investigation into its bioactive constituents and mechanisms of action.
尽管在治疗和预防方面取得了重大进展,但全球范围内对抗癌症的斗争仍在继续。本研究评估了南非夸祖鲁-纳塔尔省和东开普省的土著社区传统上用于治疗癌症及相关疾病的树皮的药理特性和抗癌活性。采用既定方案进行了植物化学筛选、高效液相色谱-二极管阵列检测(HPLC-DAD)和傅里叶变换红外光谱(FTIR)分析。通过2,2-二苯基-1-苦基肼(DPPH)清除能力和一氧化氮自由基评估抗氧化活性。使用MTT法(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐)评估抗癌活性。植物化学分析表明存在皂苷、黄酮类化合物、萜类化合物、生物碱、甾体、强心苷和鞣花单宁。HPLC-DAD分析在水提取物中检测到七个独特峰,在甲醇提取物中检测到三个独特峰。水提取物的FTIR光谱显示出对应于O-H、C=O、C=C和=C-H官能团的特征峰。在测试的提取物中,甲醇提取物在DPPH和一氧化氮方面均表现出最强的抗氧化活性,其次是乙醇提取物。甲醇提取物对DU-145癌细胞系的细胞增殖抑制作用更强,抑制率为37.8%,其次是水提取物,抑制率为36.3%。相比之下,对PC-3、SK-UT-1和AGS细胞系的活性有限。结果表明,树皮具有显著的剂量依赖性抗氧化和抗增殖活性,支持其在癌症管理中的民族药用。这些发现值得进一步研究其生物活性成分和作用机制。