Brusatol inhibits malignant phenotypes and lipid metabolism of osteosarcoma cells by regulating PI3K/AKT and MAPK pathways

IF 8.3 1区 医学 Q1 CHEMISTRY, MEDICINAL Phytomedicine Pub Date : 2025-04-01 Epub Date: 2025-02-12 DOI:10.1016/j.phymed.2025.156464
Xuhui Yuan , Shaolin Yu , Lan Lin , Yang Chen , Zhaoyang Wu , Xinyu Fang , Wenming Zhang
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Abstract

Background

Osteosarcoma (OS), the most frequent type of primary bone cancer, has a poor prognosis in metastatic cases, with overall 5-year survival rates stagnating at 20 %–30 %. This highlights the critical need for innovative therapies to address the significant survival gap between metastatic and non-metastatic cases. Brusatol (BRU), a compound extracted from Brucea javanica, has shown promising anti-tumor properties in various cancers; however, its effects on OS have yet to be investigated.

Purpose

To investigate the anti-tumor mechanisms of BRU in OS and evaluate its potential therapeutic efficacy, with a particular focus on its impact on lipid metabolism and related signaling pathways.

Methods

In vitro experiments to assess the anti-tumor effects of BRU involved colony formation, CCK-8, Transwell analysis, as well as flow cytometry. RNA sequencing was conducted to identify transcriptional changes in BRU-treated cells. The mechanism of action was investigated through analysis of lipid metabolism and key signaling pathways. Therapeutic efficacy and safety were evaluated in vivo using xenograft models.

Results

BRU significantly inhibited OS cell proliferation, migration, and invasion, while also inducing G2/M phase cell cycle arrest as well as promoting apoptosis. Transcriptome analysis revealed that BRU affected lipid metabolism-related genes and suppressed the PI3K/AKT and MAPK pathways. BRU treatment reduced fatty acid synthase expression and free fatty acid content in OS cells. In vivo experiments demonstrated that BRU effectively restricted xenograft growth.

Conclusion

This study revealed that BRU exhibits potent anti-tumor effects in OS by modulating lipid metabolism through the PI3K/AKT and MAPK pathways.

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Brusatol通过调节PI3K/AKT和MAPK通路抑制骨肉瘤细胞的恶性表型和脂质代谢
骨肉瘤(OS)是最常见的原发性骨癌类型,转移病例预后较差,总体5年生存率停滞在20% - 30%。这凸显了对创新疗法的迫切需要,以解决转移性和非转移性病例之间显著的生存差距。Brusatol (BRU)是一种从鸦嘴鸦属植物中提取的化合物,具有良好的抗肿瘤活性。然而,它对操作系统的影响还有待研究。目的探讨BRU在OS中的抗肿瘤机制,评价其潜在的治疗效果,重点研究BRU对脂质代谢及相关信号通路的影响。方法通过菌落形成、CCK-8、Transwell分析和流式细胞术等体外实验评价BRU的抗肿瘤作用。RNA测序鉴定bru处理细胞的转录变化。通过对脂质代谢和关键信号通路的分析,探讨其作用机制。使用异种移植模型在体内评估治疗效果和安全性。结果bru显著抑制OS细胞增殖、迁移和侵袭,诱导G2/M期细胞周期阻滞,促进细胞凋亡。转录组分析显示,BRU影响脂质代谢相关基因,抑制PI3K/AKT和MAPK通路。BRU处理降低了OS细胞中脂肪酸合成酶的表达和游离脂肪酸含量。体内实验表明,BRU有效地限制了异种移植物的生长。结论BRU通过PI3K/AKT和MAPK通路调节脂质代谢,在OS中表现出较强的抗肿瘤作用。
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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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