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张馨丹, 赵正刚, 周素瑾, 穆云萍, 李美蓉, 赖运浩, 萧耿苗, 李芳红, 赵子建. 重组沙门氏菌VNP20009-M对骨肉瘤的治疗作用[J]. 肿瘤防治研究, 2020, 47(12): 931-935. DOI: 10.3971/j.issn.1000-8578.2020.19.1407
引用本文: 张馨丹, 赵正刚, 周素瑾, 穆云萍, 李美蓉, 赖运浩, 萧耿苗, 李芳红, 赵子建. 重组沙门氏菌VNP20009-M对骨肉瘤的治疗作用[J]. 肿瘤防治研究, 2020, 47(12): 931-935. DOI: 10.3971/j.issn.1000-8578.2020.19.1407
ZHANG Xindan, ZHAO Zhenggang, ZHOU Sujin, MU Yunping, LI Meirong, LAI Yunhao, XIAO Gengmiao, LI Fanghong, ZHAO Zijian. Therapeutic Effect of Recombinant Salmonella VNP20009-M on Osteosarcoma[J]. Cancer Research on Prevention and Treatment, 2020, 47(12): 931-935. DOI: 10.3971/j.issn.1000-8578.2020.19.1407
Citation: ZHANG Xindan, ZHAO Zhenggang, ZHOU Sujin, MU Yunping, LI Meirong, LAI Yunhao, XIAO Gengmiao, LI Fanghong, ZHAO Zijian. Therapeutic Effect of Recombinant Salmonella VNP20009-M on Osteosarcoma[J]. Cancer Research on Prevention and Treatment, 2020, 47(12): 931-935. DOI: 10.3971/j.issn.1000-8578.2020.19.1407

重组沙门氏菌VNP20009-M对骨肉瘤的治疗作用

Therapeutic Effect of Recombinant Salmonella VNP20009-M on Osteosarcoma

  • 摘要:
    目的 研究携带甲硫氨酸酶基因的减毒沙门氏菌VNP20009-M对骨肉瘤的治疗作用及其机制。
    方法 将重组沙门氏菌VNP20009-M与骨肉瘤细胞MNNG-HOS共培养;骨肉瘤细胞MNNG-HOS、U2OS及SaoS-2均高表达甲硫氨酸酶基因后探索细胞增殖、迁移及凋亡能力的变化;构建MNNG-HOS裸鼠皮下荷瘤模型,评价不同剂量的VNP20009-M在动物模型中的治疗效果。
    结果 通过质粒PCR验证甲硫氨酸酶基因只存在于目的菌株VNP20009-M中,且具有较高的甲硫氨酸酶活性,重组沙门氏菌构建成功。VNP20009-M显著诱导骨肉瘤细胞MNNG-HOS的凋亡。相比对照组,甲硫氨酸酶基因过表达的骨肉瘤细胞增殖、迁移能力被显著抑制。VNP20009-M治疗后小鼠皮下肿瘤生长被显著抑制。
    结论 VNP20009-M可诱导骨肉瘤细胞凋亡并抑制癌细胞增殖和迁移,可以作为一种新型高效的药物为临床提供新的治疗方式。

     

    Abstract:
    Objective To investigate the therapeutic effect of attenuated salmonella VNP20009-M that carries a methioninase gene on osteosarcoma.
    Methods Recombinant salmonella VNP20009-M was co-cultured with a human osteosarcoma cell line. After the methioninase gene was overexpressed in osteosarcoma cells, cell proliferation, migration and apoptosis were detected. Finally, we evaluated the effect of the attenuated salmonella VNP20009-M on the subcutaneous xenograft in the nude mice by intratumorally injecting different dosages of VNP20009-M.
    Results It was verified by plasmid PCR that the methioninase gene was only found in the target strain VNP20009-M and had high methioninase activity. The recombinant salmonella was successfully constructed. VNP20009-M significantly induced the apoptosis of MNNG-HOS cells. Overexpression of the L-methioninase gene in the osteosarcoma cells significantly inhibited cell proliferation and migration, compared with the control group. The body weight of the subcutaneous tumor-bearing mice after VNP20009-M treatment did not change significantly, and tumor growth was significantly retarded.
    Conclusion VNP20009-M could induce the apoptosis and inhibit the proliferation and migration of osteosarcoma cancer cells, and can be a novel and highly effective drug candidate for osteosarcoma in the clinic.

     

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