Ahmmed Shakil, Bhuia Md Shimul, Chowdhury Raihan, Munshi Md Hanif, Eity Tanzila Akter, Kamli Hossam, Islam Muhammad Torequl
Department of Biochemistry and Molecular Biology, Bangladesh Agricultural University, Mymensingh, Bangladesh.
Department of Pharmacy, Gopalganj Science and Technology University, Gopalganj, Bangladesh.
Int J Food Sci. 2025 May 30;2025:2256871. doi: 10.1155/ijfo/2256871. eCollection 2025.
Due to the increasing rate of cancer and the undesirable consequences of manufactured drugs, there is a growing interest in the development of natural products as potential remedies. Ferulic acid (FA), a phenolic substance, is found naturally present in the plant's cell walls with therapeutic activities. The objective of this study is to determine the botanical sources, pharmacokinetics, and anticancer activity of FA and its derivatives, focusing on the molecular mechanism by using the data obtained from the literature database. The study's findings suggest that FA demonstrates promising anticancer effects in preclinical pharmacological test methods. The findings of the study exhibit that FA showed promising anticancer activity through underlying mechanisms, including induction of oxidative stress, cytotoxic effect, cell cycle arrest, apoptotic effect, suppression of invasion and migration, antiproliferative effect, autophagy, and genotoxic and mutagenic effect by regulating different molecular pathways like PI3K/AKT, p38/MAPK/ERK, AKT/mTOR, and NF-B signaling pathways which are involved in cancer development and cell growth. Additionally, this review indicated the pharmacokinetic properties of FA, indicating lower oral bioavailability is affected by the liver's fast conjugation process; this limitation is overcome by applying a nanoformulation of FA. However, additional clinical investigations are recommended to determine the appropriate therapeutic effectiveness, safety, and human dosage.
由于癌症发病率不断上升以及合成药物带来的不良后果,人们对开发天然产物作为潜在治疗方法的兴趣日益浓厚。阿魏酸(FA)是一种酚类物质,天然存在于植物细胞壁中,具有治疗活性。本研究的目的是确定FA及其衍生物的植物来源、药代动力学和抗癌活性,利用从文献数据库获得的数据重点关注其分子机制。该研究结果表明,在临床前药理测试方法中,FA显示出有前景的抗癌效果。该研究结果表明,FA通过潜在机制表现出有前景的抗癌活性,包括诱导氧化应激、细胞毒性作用、细胞周期阻滞、凋亡作用、抑制侵袭和迁移、抗增殖作用、自噬以及通过调节参与癌症发展和细胞生长的PI3K/AKT、p38/MAPK/ERK、AKT/mTOR和NF-κB信号通路等不同分子途径产生的遗传毒性和诱变作用。此外,本综述指出了FA的药代动力学特性,表明较低的口服生物利用度受肝脏快速结合过程的影响;通过应用FA的纳米制剂克服了这一局限性。然而,建议进行更多的临床研究以确定适当的治疗效果、安全性和人体剂量。