Gurning Kasta, Primahana Gian, Astuti Endang, Haryadi Winarto
Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia.
Department of Pharmacy, Sekolah Tinggi Ilmu Kesehatan Senior Medan, Medan 20141, Indonesia.
Adv Pharmacol Pharm Sci. 2025 Jul 11;2025:5946648. doi: 10.1155/adpp/5946648. eCollection 2025.
Lung cancer and breast cancer are two types of cancer that cause and contribute to the highest mortality rate in the world. The development of anticancer agents that have high efficacy and relatively low side effects continues to be developed and is the focus of research, and one of the raw materials that can be explored is active compounds sourced from natural materials, one of which is plants. This study aims to isolate active compounds from bangun-bangun (, Lour.) leaves, test cytotoxicity as an antilung and breast cancer agent in vitro, and conduct molecular docking studies with a network pharmacology approach on the pathways in cancer. Research methods include extraction by the maceration method and purification by column chromatography, anticancer activity testing is carried out by the microtetrazolium (MTT) test method against lung cancer (A549), breast cancer (MCF-7), and normal cells (CV-1), and molecular docking studies are carried out with a network pharmacology approach focused on proteins in cancer pathways. The results of the active isolate (I) from -hexane extract showed the best activity against lung cancer/A549 cells (IC 31.74 μg/mL), and the active isolate (I) from ethyl acetate extract showed the best activity against breast cancer/MCF-7 cells (IC 80.05 μg/mL) and showed no toxicity to normal cells (CV-1). The results of the bioinformatic study are with a network pharmacology approach on the cancer pathway of bioactive compounds from each isolate target the matrix metalloproteinase-2 (MMP-2) protein. The content of bioactive compounds from leaves shows the potential to be used as active agents in the treatment of lung cancer and breast cancer in the future.
肺癌和乳腺癌是导致全球最高死亡率且在死亡率方面占比很大的两种癌症类型。高效且副作用相对较低的抗癌药物的研发一直在持续进行,并且是研究的重点,其中一种可探索的原材料是源自天然物质的活性化合物,植物就是其中之一。本研究旨在从地桃花(Urena lobata Linn.)叶中分离活性化合物,体外测试其作为抗肺癌和乳腺癌药物的细胞毒性,并采用网络药理学方法对癌症相关通路进行分子对接研究。研究方法包括浸渍法提取和柱色谱法纯化,通过微量四氮唑蓝(MTT)试验方法对肺癌(A549)、乳腺癌(MCF - 7)和正常细胞(CV - 1)进行抗癌活性测试,以及采用网络药理学方法针对癌症通路中的蛋白质进行分子对接研究。从正己烷提取物中得到的活性分离物(I)对肺癌/A549细胞显示出最佳活性(IC 31.74μg/mL),从乙酸乙酯提取物中得到的活性分离物(I)对乳腺癌/MCF - 7细胞显示出最佳活性(IC 80.05μg/mL),并且对正常细胞(CV - 1)无毒性。生物信息学研究结果表明,采用网络药理学方法对每种分离物的生物活性化合物在癌症通路上的研究靶向基质金属蛋白酶 - 2(MMP - 2)蛋白。地桃花叶中生物活性化合物的含量显示出未来有潜力用作治疗肺癌和乳腺癌的活性剂。