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柴胡皂苷作为抗癌药物靶向细胞程序性死亡:作用机制与未来展望。

Saikosaponins Targeting Programmed Cell Death as Anticancer Agents: Mechanisms and Future Perspectives.

机构信息

Department of Clinical Laboratory Medicine Center, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, 200437, People's Republic of China.

出版信息

Drug Des Devel Ther. 2024 Aug 21;18:3697-3714. doi: 10.2147/DDDT.S470455. eCollection 2024.

Abstract

Saikosaponins (SS), which are major bioactive compounds in Radix Bupleuri, have long been used clinically for multicomponent, multitarget, and multipathway therapeutic strategies. Programmed cell death (PCD) induction is among the multiple mechanisms of SS and mediates the anticancer efficacy of this drug family. Although SS show promise for anticancer therapy, the available data to explain how SS mediate their key anticancer effects through PCD (apoptosis, autophagy, ferroptosis, and pyroptosis) remain limited and piecemeal. This review offers an extensive analysis of the key pathways and mechanisms involved in PCD and explores the importance of SS in cancer. We believe that high-quality clinical trials and a deeper understanding of the pharmacological targets involved in the signalling cascades that govern tumour initiation and progression are needed to facilitate the development of innovative SS-based treatments. Elucidating the specific anticancer pathways activated by SS and further clarifying how comprehensive therapies lead to cross-link among the different types of cell death will inspire the clinical translation of SS as cancer treatments.

摘要

柴胡皂苷(SS)是柴胡中的主要生物活性化合物,长期以来一直被临床用于多成分、多靶点和多途径的治疗策略。程序性细胞死亡(PCD)诱导是 SS 的多种机制之一,介导了该药物家族的抗癌功效。尽管 SS 显示出抗癌治疗的潜力,但目前可用的数据还不足以解释 SS 如何通过 PCD(细胞凋亡、自噬、铁死亡和细胞焦亡)来介导其关键的抗癌作用。本综述广泛分析了 PCD 涉及的关键途径和机制,并探讨了 SS 在癌症中的重要性。我们认为,需要高质量的临床试验和对调控肿瘤发生和进展的信号级联中涉及的药理学靶点的更深入理解,以促进基于 SS 的创新治疗方法的发展。阐明 SS 激活的特定抗癌途径,并进一步阐明综合治疗如何导致不同类型细胞死亡之间的交联,将激发 SS 作为癌症治疗的临床转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece3/11345020/9a4d34ce1a44/DDDT-18-3697-g0001.jpg

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