医学研究与教育 ›› 2023, Vol. 40 ›› Issue (1): 1-9.DOI: 10.3969/j.issn.1674-490X.2023.01.001

• 基础医学 •    下一篇

人参皂苷Rg1联合阿霉素对K562/ADR细胞增殖及耐药的影响

唐紫云1,李敏瑞1,张成桂2,刘衡3,周玥1   

  1. 1.大理大学组织学与胚胎学教研室, 云南 大理 671000;
    2.云南省昆虫生物医药研发重点实验室, 云南 大理 671000;
    3.药用特种昆虫开发国家地方联合工程研究中心, 云南 大理 671000
  • 收稿日期:2022-12-12 出版日期:2023-02-25 发布日期:2023-02-25
  • 通讯作者: 周玥(1979—),女,云南大理人,教授,博士,硕士生导师,主要从事中药药理学研究。E-mail: zhouyue_120@sina.com
  • 作者简介:唐紫云(1996—),女,云南昆明人,在读硕士,主要从事中药药理学研究。 E-mail: 1597345218@qq.com
  • 基金资助:
    国家自然科学基金-地区项目(81860038,81660731);国家自然科学基金-面上项目(81873103)

  • Received:2022-12-12 Online:2023-02-25 Published:2023-02-25

摘要: 目的 探究人参皂苷Rg1对人慢性髓细胞白血病耐阿霉素(adriamycin,ADR)细胞K562/ADR增殖的影响及其对K562/ADR细胞的耐药逆转作用。方法 CCK-8法检测不同浓度的人参皂苷Rg1对K562/ADR细胞增殖的影响;CCK-8法检测人参皂苷Rg1与ADR联用对K562/ADR细胞增殖的影响,计算半数抑制浓度(IC50)和逆转倍数;集落形成实验检测人参皂苷Rg1联合ADR对K562/ADR细胞集落形成能力的影响;流式细胞术检测人参皂苷Rg1联合ADR对K562/ADR细胞周期的影响。结果 与对照组相比,各浓度和作用时间的人参皂苷Rg1均可抑制K562/ADR细胞增殖(P<0.001),当人参皂苷Rg1浓度为120 μg/mL,作用时间为48 h时,细胞增殖抑制率最高(P<0.05);与单用ADR相比,人参皂苷Rg1联合ADR作用48 h后,K562/ADR细胞IC50值明显下降(P<0.05),人参皂苷Rg1对K562/ADR细胞的耐药逆转倍数为2.34;与对照组和ADR或人参皂苷Rg1单药作用相比,人参皂苷Rg1联合ADR作用能明显抑制K562/ADR细胞集落形成(P<0.05);与ADR或人参皂苷Rg1单药作用相比,人参皂苷Rg1联合ADR作用可以将细胞周期阻滞在G0/G1期。结论 人参皂苷Rg1联合ADR能明显抑制K562/ADR细胞增殖并逆转K562/ADR细胞对ADR的耐药性,这可能与细胞周期阻滞于G0/G1期有关。

关键词: 人参皂苷Rg1, 阿霉素, K562/ADR细胞, 细胞周期, 耐药

Abstract: Objective To investigate the effect of ginsenoside Rg1 on the proliferation of adriamycin(ADR)-resistant K562/ADR cells in human chronic myeloid leukemia(CML)and its reversal of drug resistance in K562/ADR cells. Methods CCK-8 assay was used to detect the effects of different concentrations of ginsenoside Rg1 on the proliferation of K562/ADR cells. CCK-8 assay was used to detect the effects of ginsenoside Rg1 combined with ADR on the proliferation of K562/ADR cells, and the half maximal inhibitory concentration(IC50)and reversal fold were calculated. Colony formation assay was used to detect the effects of ginsenoside Rg1 combined with ADR on the colony formation ability of K562/ADR cells. Flow cytometry was used to detect the effects of ginsenoside Rg1 combined with ADR on the cell cycle of K562/ADR cells. Results Compared with the control group, the proliferation inhibition rate of K562/ADR cells treated with 120 μg/ml ginsenoside Rg1 for 48 h was significantly increased(P<0.001). Compared with the ADR alone group, the IC50 value of ginsenoside Rg1 combined with ADR for 48 h decreased significantly in K562/ADR cells(P<0.05), and the fold reversal of ginsenoside Rg1 resistance to K562/ADR cells was 2.34. Compared with the control group and ADR or ginsenoside Rg1 alone group, ginsenoside Rg1 combined with ADR could significantly inhibit K562/ADR cell colony formation(P<0.05). Compared with the ADR or ginsenoside Rg1 alone group, ginsenoside Rg1 combined with ADR could arrest the cell cycle in G0/G1 phase. Conclusion Ginsenoside Rg1 combined with ADR can significantly inhibit the proliferation of K562/ADR cells and reverse the resistance of K562/ADR cells to ADR, which may be related to the cell cycle arrest in G0/G1 phase.

Key words: ginsenoside Rg1, adriamycin, K562/ADR cells, cell cycle, drug resistance

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