Santos Edvania Emannuelle Pinheiro, de Oliveira Andrade Maria Lorena, Dos Santos Nascimento Igor José, Cibulski Samuel Paulo, da Silva Alves Harley
Programa de Pós-Graduação em Ciências Farmacêuticas. Universidade Estadual da Paraíba. Rua Baraúnas, 351, Bairro Universitário 58429-500 Campina Grande-PB, Brasil.
Curr Top Med Chem. 2025;25(4):378-394. doi: 10.2174/0115680266315197241015101801.
The search for effective cancer therapies highlights saponins, natural plant-derived compounds, as promising anticancer agents. These compounds induce apoptosis in cancer cells by activating caspases, essential enzymes for cell death. For example, Soyasapogenol B from and Astragaloside IV from effectively trigger apoptosis in cancer cells. Additionally, saponins, such as Compound K from American ginseng and Saikosaponin from , affect extrinsic and intrinsic pathways, including mitochondrial release of cytochrome C and activation of caspase-9. Ziyuglycoside II also acts on both pathways and activates the ROS/JNK pathway. Understanding these mechanisms provides promising prospects for developing more specific and safer anticancer therapies. The review utilized the ScienceDirect, PubMed, and Google Scholar databases. It was found that original articles and reviews from journals indexed in these sources emphasized the antitumor capabilities of saponins and discussed their role in apoptosis induction and caspase activation. The activation of caspases by saponins in the apoptotic pathway involves two main pathways: the extrinsic pathway is initiated by external signals that activate caspase-8, while the intrinsic pathway starts with internal stimuli, causing the release of cytochrome c and the activation of caspase-9. These pathways both lead to the activation of effector caspases (caspases 3, 6, and 7), culminating in apoptosis, an essential process for maintaining cellular balance and eliminating damaged cells. Identifying saponins in the context of cancer and their mechanisms of action is an ever-evolving field. Future research may lead to more targeted and personalized therapies, highlighting the collaboration between basic and clinical research in this promising area of medicine.
对有效癌症治疗方法的探索凸显了皂苷这种天然植物衍生化合物,它是很有前景的抗癌剂。这些化合物通过激活半胱天冬酶(细胞死亡所必需的酶)来诱导癌细胞凋亡。例如,来自[具体植物1]的大豆皂醇B和来自[具体植物2]的黄芪甲苷能有效触发癌细胞凋亡。此外,皂苷,如来自西洋参的化合物K和来自[具体植物3]的柴胡皂苷,会影响外在和内在途径,包括细胞色素C从线粒体释放以及半胱天冬酶-9的激活。紫萸糖苷II也作用于这两条途径并激活ROS/JNK途径。了解这些机制为开发更具特异性和安全性的抗癌疗法提供了有前景的方向。该综述利用了ScienceDirect、PubMed和谷歌学术数据库。研究发现,这些来源索引的期刊中的原创文章和综述强调了皂苷的抗肿瘤能力,并讨论了它们在诱导凋亡和激活半胱天冬酶中的作用。皂苷在凋亡途径中激活半胱天冬酶涉及两条主要途径:外在途径由激活半胱天冬酶-8的外部信号启动,而内在途径始于内部刺激,导致细胞色素c释放和半胱天冬酶-9激活。这些途径都会导致效应半胱天冬酶(半胱天冬酶3、6和7)的激活,最终导致凋亡,这是维持细胞平衡和清除受损细胞的重要过程。在癌症背景下识别皂苷及其作用机制是一个不断发展的领域。未来的研究可能会带来更具针对性和个性化的疗法,凸显基础研究与临床研究在这个有前景的医学领域的合作。