Pharmaceutical Sciences and Technology Program, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok 10330, Thailand.
Department of Biochemistry, Faculty of Health Sciences, Islamic University in Uganda, Kampala P.O. Box 7689, Uganda.
Molecules. 2022 Nov 15;27(22):7902. doi: 10.3390/molecules27227902.
The most prevalent lung cancer is non-small cell lung cancer (NSCLC). This lung cancer type often develops other organ-specific metastases that are critical burdens in the treatment process. Orchid species in the genus Vanda have shown their potential in folkloric medication of diverse diseases but not all its species have been investigated, and little is known about their anticancer activities against NSCLC. Here, we firstly profiled the specialized metabolites of Vanda bensonii and examined their capability to inhibit growth and metastasis of NSCLC using NCI-H460 cells as a study model. Four phytochemicals, including phloretic acid methyl ester (1), cymbinodin-A (2), ephemeranthoquinone B (3), and protocatechuic acid (4), were isolated from the whole plant methanolic extract of V. bensonii. The most distinguished cytotoxic effect on NCI-H460 cells was observed in the treatments with crude methanolic extract and compound 2 with the half maximal inhibitory concentrations of 40.39 μg mL−1 and 50.82 μM, respectively. At non-cytotoxic doses (10 μg mL−1 or 10 μM), only compound 1 could significantly limit NCI-H460 cell proliferation when treated for 48 h, while others excluding compound 4 showed significant reduction in cell proliferation after treating for 72 h. Compound 1 also significantly decreased the migration rate of NCI-H460 cells examined through a wound-healing assay. Additionally, the crude extract and compound 1 strongly affected survival and growth of NCI-H460 cells under anchorage-independent conditions. Our findings proved that natural products from V. bensonii could be promising candidates for the future pharmacotherapy of NSCLC.
最常见的肺癌是非小细胞肺癌(NSCLC)。这种肺癌类型通常会发展出其他特定器官的转移,这在治疗过程中是一个关键的负担。万代兰属的兰花物种在治疗各种疾病的民间药物中显示出了它们的潜力,但并非所有物种都得到了研究,人们对它们针对 NSCLC 的抗癌活性知之甚少。在这里,我们首先对万代兰的特征代谢产物进行了分析,并使用 NCI-H460 细胞作为研究模型,研究了它们抑制 NSCLC 生长和转移的能力。从万代兰全植物甲醇提取物中分离得到了 4 种植物化学物质,包括 phloretic acid methyl ester(1)、cymbinodin-A(2)、ephemeranthoquinone B(3)和 protocatechuic acid(4)。在对 NCI-H460 细胞的处理中,粗甲醇提取物和化合物 2 表现出了最显著的细胞毒性,其半最大抑制浓度分别为 40.39 μg mL−1和 50.82 μM。在非细胞毒性剂量(10 μg mL−1或 10 μM)下,只有化合物 1 能在处理 48 h 后显著抑制 NCI-H460 细胞的增殖,而其他化合物(不包括化合物 4)在处理 72 h 后能显著降低细胞增殖率。化合物 1 还显著降低了划痕实验中 NCI-H460 细胞的迁移率。此外,粗提取物和化合物 1 在非锚定依赖条件下强烈影响 NCI-H460 细胞的存活和生长。我们的研究结果证明,万代兰的天然产物可能是 NSCLC 未来药物治疗的有前途的候选药物。