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薯蓣皂苷 AIII 通过抑制内吞途径破坏细胞-细胞外基质相互作用。

Timosaponin AIII Disrupts Cell-Extracellular Matrix Interactions through the Inhibition of Endocytic Pathways.

机构信息

Department of Pharmacology, Faculty of Medicine, Oita University.

Clinical Engineering Research Center, Faculty of Medicine, Oita University.

出版信息

Biol Pharm Bull. 2024;47(10):1648-1656. doi: 10.1248/bpb.b24-00403.

Abstract

Timosaponin AIII (TAIII), a steroidal saponin isolated from the root of Anemarrhena asphodeloides Bunge, exhibits various pharmacological activities, including anti-cancer properties. TAIII inhibits the migration and invasion of various cancer cell types. However, the mechanism underlying how TAIII regulates the motility of cancer cells remains incompletely understood. In this study, we demonstrate that TAIII disrupted cell-extracellular matrix (ECM) interactions by inhibiting internalization of cell surface proteins, such as integrins. We found that TAIII inhibited cell adhesion on various ECMs. Structure-activity relationship analysis demonstrated that TAIII exhibited unique activity among the saponins from Anemarrhena asphodeloides Bunge and that the number and position of saccharide moieties were important for TAIII to exert its activity. Time lapse imaging revealed that TAIII also suppressed cell spreading on the ECM, membrane ruffling, and lamellipodia formation. Furthermore, we examined integrin β1 behaviors in response to TAIII treatment and found that TAIII blocked its internalization. These findings contribute to delineating the potential molecular mechanisms by which TAIII exerts anti-metastatic activity.

摘要

知母皂苷 AIII(TAIII)是从知母根中分离得到的一种甾体皂苷,具有多种药理活性,包括抗癌作用。TAIII 抑制多种癌细胞类型的迁移和侵袭。然而,TAIII 如何调节癌细胞运动的机制尚不完全清楚。在这项研究中,我们证明 TAIII 通过抑制细胞表面蛋白(如整合素)的内化来破坏细胞-细胞外基质(ECM)相互作用。我们发现 TAIII 抑制了各种 ECM 上的细胞黏附。构效关系分析表明,TAIII 在知母皂苷中表现出独特的活性,并且糖基的数量和位置对于 TAIII 发挥其活性很重要。延时成像显示 TAIII 还抑制了细胞在 ECM 上的扩展、膜皱襞和片状伪足的形成。此外,我们检测了整合素 β1 对 TAIII 处理的反应行为,发现 TAIII 阻断了其内化。这些发现有助于描绘 TAIII 发挥抗转移活性的潜在分子机制。

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