Genipin Inhibits the Development of Osteosarcoma through PI3K/AKT Signaling Pathway

京尼平 骨肉瘤 MTT法 流式细胞术 PI3K/AKT/mTOR通路 癌症研究 细胞凋亡 蛋白激酶B 庆大霉素保护试验 细胞周期蛋白D1 化学 体内 细胞生长 免疫印迹 分子生物学 生物 细胞周期 生物化学 生物技术 基因 壳聚糖
作者
Xiongjie Huang,Habu Jiwa,Jingtao Xu,Jun Zhang,Yanran Huang,Xiaoji Luo
出处
期刊:Current Pharmaceutical Design [Bentham Science]
卷期号:29 (16): 1300-1310 被引量:2
标识
DOI:10.2174/1381612829666230508145533
摘要

Background: Osteosarcoma is a highly invasive and early metastatic tumor. At present, the toxic and side effects of chemotherapy affect the quality of life of cancer patients to varying degrees. Genipin is an extract of the natural medicine gardenia with various pharmacological activities. Objective: The purpose of this study was to investigate the effect of Genipin on osteosarcoma and its potential mechanism of action. Methods: Crystal violet staining, MTT assay and colony formation assay were used to detect the effect of genipin on the proliferation of osteosarcoma. The effects of vitexin on migration and invasion of osteosarcoma were detected by scratch healing assay and transwell assay. Hoechst staining and flow cytometry were used to detect the effect of genipin on apoptosis of osteosarcoma cells. The expression of related proteins was detected by Western blot. An orthotopic tumorigenic animal model was used to verify the effect of genipin on osteosarcoma in vivo. Results: The results of crystal violet staining, MTT method and colony formation method proved that genipin significantly inhibited the proliferation of osteosarcoma cells. The results of the scratch healing assay and transwell assay showed that gen significantly inhibited the migration and invasion of osteosarcoma cells. The results of Hoechst staining and flow cytometry showed that genipin significantly promoted the apoptosis of osteosarcoma cells. The results of animal experiments show that genipin has the same anti-tumor effect in vivo. Genipin may inhibit the growth of osteosarcoma through PI3K/AKT signaling. Conclusion: Genipin can inhibit the growth of human osteosarcoma cells, and its mechanism may be related to the regulation of PI3K/AKT signaling pathway.

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