基础医学与临床 ›› 2022, Vol. 42 ›› Issue (8): 1200-1205.doi: 10.16352/j.issn.1001-6325.2022.08.1200

• 研究论文 • 上一篇    下一篇

莪术醇抑制人骨肉瘤细胞系的增殖和促凋亡

江宁1, 郭钧2*, 刘铖1, 周举1   

  1. 1.中国人民解放军总医院第五医学中心(原中国人民解放军第307医院)骨科,北京 100007;
    2.清华大学第一附属医院 骨科,北京 100016
  • 收稿日期:2022-02-22 修回日期:2022-05-06 出版日期:2022-08-05 发布日期:2022-08-02
  • 通讯作者: *gzd713@163.com
  • 基金资助:
    国家自然科学基金(3167080224)

Curcumol inhibits proliferation and promotes apoptosis of human osteosarcoma cell lines

JIANG Ning1, GUO Jun2*, LIU Cheng1, ZHOU Ju1   

  1. 1. Department of Orthopedics, the Fifth Medical Center, Chinese People’ s Liberation Army General Hospital(the former 307th hospital of PLA), Beijing 100007;
    2. Department of Orthopedics, the First Affiliated Hospital of Tsinghua University, Beijing 100016, China
  • Received:2022-02-22 Revised:2022-05-06 Online:2022-08-05 Published:2022-08-02
  • Contact: *gzd713@163.com

摘要: 目的 探究莪术醇对人骨肉瘤细胞系MG-63和U2OS体外增殖、凋亡的影响和作用机制。方法 将MG-63细胞和U2OS细胞分为对照组、莪术醇20、40、80和160 μmol/L干预组;MTT法检测MG-63、U2OS细胞增殖;Transwell小室法检测细胞迁移和侵袭;流式细胞测量细胞凋亡;RT-qPCR和Western blot检测凋亡相关蛋白Bax、Bcl2、caspase和β-catenin的mRNA和蛋白表达。结果 莪术醇呈浓度依赖性地抑制MG-63和U2OS细胞增殖,IC50值分别为128.03 μmol/L、117.95 μmol/L。与对照组相比,莪术醇显著抑制MG-63、U2OS细胞的体外迁移和侵袭(P<0.05),并诱导细胞凋亡(P<0.05)。与对照组相比,莪术醇组促进Bax、caspase 3表达,抑制Bcl2表达(P<0.05),MG-63、U2OS细胞内β-catenin的mRNA表达水平和蛋白表达均被显著抑制(P<0.05)。结论 莪术醇显著抑制人骨肉瘤细胞系MG-63、U2OS增殖,诱导细胞凋亡。

关键词: 莪术醇, β-catenin, 骨肉瘤, 细胞增殖, 细胞凋亡

Abstract: Objective To explore the effects and mechanism of curcumol on in vitro proliferation and apoptosis of human osteosarcoma cell lines MG-63 and U2OS. Methods MG-63 cells and U2OS cells were divided into control group and 20, 40, 80 and 160 μmol/L curcumol groups. MTT assay was used to detect the proliferation levels of MG-63 and U2OS cells, and Transwell chamber assay was used for cell migration and invasion and flow cytometry was used for cell apoptosis. RT-qPCR and Western blot were applied to detect the mRNA and protein expressions of apoptosis-related proteins Bax, Bcl2, caspase and β-catenin. Results Curcumol inhibited the proliferation of MG-63 and U2OS cells in a concentration-dependent manner, and the IC50 values were 128.03 μmol/L and 117.95 μmol/L respectively. Compared with the control group, curcumol significantly inhibited the in vitro migration and invasion of MG-63 and U2OS cells (P<0.05) and induced the cell apoptosis (P<0.05). Compared with the control group, expressions of Bax and caspase 3 were promoted while expression of Bcl2 was inhibited in curcumol groups (P<0.05). The mRNA and protein expressions of β-catenin in MG-63 and U2OS cells were signifi- cantly inhibited (P<0.05). Conclusions Curcumol significantly inhibits proliferation and induces apoptosis of human osteosarcoma cell lines MG-63 and U2OS.

Key words: Curcumol, β-catenin, osteosarcoma, cell proliferation, cell apoptosis

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