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天然产物大豆苷元通过抑制LRP5介导的GSK-3β/c-Myc信号通路抑制胶质瘤发展。

Natural Product Daidzin Inhibits Glioma Development via Suppressing the LRP5-Mediated GSK-3β/c-Myc Signaling Pathway.

作者信息

Pan Yijing, Wang Shunshun, Duan Guoliang, Wu Jiaqin, Feng Fan, Chen Lin, Li Anzheng, Xu Kang, Wang Chunli, Fan Shibing

机构信息

Hubei Provincial Engineering Technology Research Center for Chinese Medicine Processing, School of Pharmacy, Hubei University of Chinese Medicine, Wuhan, China.

Chongqing University Three Gorges Hospital, and School of Medicine Chongqing University, Chongqing, People's Republic of China.

出版信息

Biofactors. 2025 May-Jun;51(3):e70025. doi: 10.1002/biof.70025.

Abstract

Daidzin (DZN) is a natural flavonoid compound derived from soybeans that has recently been recognized for its potential antitumor properties. In traditional Chinese medicine, soybeans and their extracts are extensively used to prevent and treat various diseases. To evaluate the therapeutic efficacy of DZN on human glioblastoma through in vivo and in vitro experiments, and through multi-omics analyses to elucidate potential molecular mechanisms. Cell viability of LN-229 and U-87MG glioblastoma cells was assessed using the CCK-8 assay. Protein and mRNA levels of proliferation and apoptosis-related genes were analyzed via Western blotting and qPCR. Metabolomics and transcriptomics identified key pathways and targets, which were confirmed by in-cell Western blotting and expression correlation analysis. The in vivo antitumor effects of DZN were evaluated in nude mice with LN-229 tumors. DZN treatment reduced cell viability, migration, and survival in a dose-dependent manner, demonstrating strong antitumor effects in both in vitro and in vivo models. Multi-omics analysis identified amino acid metabolism and ubiquitin-mediated proteolysis as key mechanisms. Bioinformatics highlighted LRP5 as a prognostic biomarker in glioblastoma. DZN decreased LRP5 activity, downregulated p-GSK-3β, and promoted c-Myc degradation, thereby inhibiting the Wnt signaling pathway. In vivo, DZN significantly reduced tumor size and Ki67 expression. These findings highlight LRP5 as a promising therapeutic target, with DZN emerging as a potent LRP5 inhibitor and exhibiting significant antitumor effects in glioblastoma.

摘要

大豆苷(DZN)是一种从大豆中提取的天然黄酮类化合物,最近因其潜在的抗肿瘤特性而受到关注。在传统中医中,大豆及其提取物被广泛用于预防和治疗各种疾病。通过体内和体外实验评估DZN对人胶质母细胞瘤的治疗效果,并通过多组学分析阐明潜在的分子机制。使用CCK-8法评估LN-229和U-87MG胶质母细胞瘤细胞的活力。通过蛋白质印迹法和qPCR分析增殖和凋亡相关基因的蛋白质和mRNA水平。代谢组学和转录组学确定了关键途径和靶点,并通过细胞内蛋白质印迹法和表达相关性分析进行了验证。在携带LN-229肿瘤的裸鼠中评估DZN的体内抗肿瘤作用。DZN处理以剂量依赖性方式降低细胞活力、迁移和存活率,在体外和体内模型中均显示出强大的抗肿瘤作用。多组学分析确定氨基酸代谢和泛素介导的蛋白水解为关键机制。生物信息学强调LRP5是胶质母细胞瘤的预后生物标志物。DZN降低LRP5活性,下调p-GSK-3β,并促进c-Myc降解,从而抑制Wnt信号通路。在体内,DZN显著减小肿瘤大小并降低Ki67表达。这些发现突出了LRP5作为一个有前景的治疗靶点,DZN作为一种有效的LRP5抑制剂,在胶质母细胞瘤中显示出显著的抗肿瘤作用。

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