College of Pharmacy, Shandong University of Traditional Chinese Medicine, Ji'nan, 250355, China.
College of Pharmacy, Shandong University of Traditional Chinese Medicine, Ji'nan, 250355, China.
Phytomedicine. 2021 Jun;86:153560. doi: 10.1016/j.phymed.2021.153560. Epub 2021 Mar 28.
The dried fruits of Brucea javanica (L.) Merr (BJ) is being widely investigated, both in lab and in clinic, to explore its potential anticancer activity and molecular mechanism involved.
We appraised the available literature and suggested the future research directions to improve the medicinal value of BJ.
In this review, we have summarized the scientific findings from experimental and clinical studies regarding the anticancer activity and mechanisms.
Numerous studies have reported that BJ exerts anticancer effect on various types of cancer lines through inhibiting cell proliferation, inducing apoptosis, inhibiting migration/invasion, inducing autophagy and restraining angiogenesis. Brucea javanica triggers the generation of reactive oxygen species (ROS), release of cytochrome C, activation of mitochondrial apoptosis pathway and regulation of a series of signal pathways and proteins related to cancer. The molecular mechanism involved are inhibiting the PI3K/Akt/mTOR, NF-κB and Nrf2-Notch1 pathways; up or down modulating the levels of p53, p62, p21, Bax, and Bcl-2 respectively, and inhibiting the expression of matrix metalloproteinases (MMPs), vascular endothelial growth factor (VEGF), cyclooxygenase-2 (COX-2) and prostaglandin E2 (PGE2). Brucea javanica's efficacy in treating cancer patients either as a main or supportive treatment is also discussed in this review.
This review will serve as a comprehensive resource of BJ's potential as anticancer agent and its molecular pathways. The analysis of the literature suggests that BJ can serve as a potential candidate for the treatment of cancer.
鸦胆子(Brucea javanica(L.)Merr)的干果正在实验室和临床中广泛研究,以探索其潜在的抗癌活性和涉及的分子机制。
我们评估了现有文献,并提出了未来的研究方向,以提高鸦胆子的药用价值。
在本综述中,我们总结了关于抗癌活性和机制的实验和临床研究的科学发现。
许多研究报告称,鸦胆子通过抑制细胞增殖、诱导细胞凋亡、抑制迁移/侵袭、诱导自噬和抑制血管生成,对多种类型的癌细胞系发挥抗癌作用。鸦胆子引发活性氧(ROS)的产生、细胞色素 C 的释放、线粒体凋亡途径的激活以及与癌症相关的一系列信号通路和蛋白的调节。涉及的分子机制包括抑制 PI3K/Akt/mTOR、NF-κB 和 Nrf2-Notch1 通路;分别上调或下调 p53、p62、p21、Bax 和 Bcl-2 的水平,并抑制基质金属蛋白酶(MMPs)、血管内皮生长因子(VEGF)、环氧化酶-2(COX-2)和前列腺素 E2(PGE2)的表达。本综述还讨论了鸦胆子作为主要或辅助治疗癌症患者的疗效。
本综述将成为鸦胆子作为抗癌剂及其分子途径的潜在功效的综合资源。文献分析表明,鸦胆子可以作为治疗癌症的潜在候选药物。