肝癌;锰离子;细胞增殖;细胞凋亡," /> 肝癌;锰离子;细胞增殖;细胞凋亡,"/> Liver cancer,Manganese ion,Cell proliferation,Cell apoptosis,"/> 锰离子对肝癌细胞增殖及凋亡的影响

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中国癌症防治杂志 ›› 2024, Vol. 16 ›› Issue (1): 62-66.doi: 10.3969/j.issn.1674-5671.2024.01.10

• 基础研究 • 上一篇    下一篇

锰离子对肝癌细胞增殖及凋亡的影响

  

  1. 广西医科大学研究生院;广西医科大学附属肿瘤医院日间病房 
  • 出版日期:2024-02-25 发布日期:2024-02-26
  • 通讯作者: 刘志辉 E-mail:lzhh101@sina.com
  • 基金资助:
     广西自然科学基金项目(2018GXNSFAA281129)

Effects of manganese ion on proliferation and apoptosis of  liver cancer cells

  • Online:2024-02-25 Published:2024-02-26

摘要: 目的 探讨锰离子(Mn2+)在肝癌细胞增殖及凋亡中的作用。方法 采用不同浓度(1、4、16、64、256、1 024 μmol/L)锰离子溶液处理肝癌Huh7、HepG2.2.15细胞,以未经锰离子溶液处理的相应细胞为对照组。采用CCK⁃8实验和平板克隆形成实验检测细胞增殖能力,流式细胞术检测细胞凋亡情况。结果 CCK⁃8实验结果显示,与对照组相比,Huh7细胞在除1 μmol/L浓度外的其余浓度锰离子溶液处理下细胞增殖活力均降低(均P<0.05),HepG2.2.15细胞在除1 μmol/L和4 μmol/L浓度外的其余浓度锰离子溶液处理下细胞增殖活力均降低(均P<0.0001),且随着锰离子浓度增大,对两组细胞增殖活力的抑制作用越显著;平板克隆形成实验结果显示,Huh7细胞在除1 μmol/L和4 μmol/L浓度外的其余浓度锰离子溶液处理下细胞克隆形成数均降低(均P<0.01),HepG2.2.15细胞在除1 μmol/L浓度外的其余浓度锰离子溶液处理下细胞克隆形成数均降低(均P<0.0001),且随着锰离子浓度的增大,细胞克隆形成数量降低越明显;流式细胞术检测结果显示,Huh7细胞和HepG2.2.15细胞的凋亡率均在64 μmol/L和1 024 μmol/L浓度锰离子溶液处理下差异有统计学意义(均P<0.01),且随着锰离子浓度的增大凋亡率越高。结论 锰离子能抑制肝癌细胞增殖和细胞克隆形成,并诱导肝癌细胞凋亡。

关键词: 肝癌;锰离子;细胞增殖;细胞凋亡')">">肝癌;锰离子;细胞增殖;细胞凋亡

Abstract: Objective To investigate the effects of manganese ion (Mn2+) on the proliferation and apoptosis of liver cancer cells. Methods Hepatoma Huh7 and HepG2.2.15 cells were treated with different concentrations (1, 4, 16, 64, 256  and 1 024 μmol/L, respectively) of Mn2+ solutions, and the corresponding cells without Mn2+ solution treatment were used as the control group. The cell proliferation was detected by CCK⁃8 assay and colony formation assay, and the apoptosis rate was detected by flow cytometry. Results The results of CCK⁃8 assay showed that compared with the control group, the cell proliferation activity of Huh7 cells was decreased under the treatment of all the conentrations of Mn2+ solution except the one of 1 μmol/L (all P<0.05); the proliferation activity of HepG2.2.15 cells was significantly decreased under the treatment of all the conentrations of  Mn2+ solutions except those of 1 μmol/L and 4 μmol/L (all P<0.0001), and with the increase of Mn2+ concentration, the inhibition of cell proliferation in both groups was more and more significant. The results of colony formation assay showed that the colonies number of Huh7 cells was decreased under the treatment of all the Mn2+ solution except those of 1 μmol/L and 4 μmol/L (all P<0.01); the colonies number of HepG2.2.15 cells was decreased under the treatment of all the Mn2+ solution except the one of 1 μmol/L (all P<0.0001), and with the increase of Mn2+ concentration, the colonies number of cell decreased significantly. The results of apoptosis experiment showed that the apoptosis rates of Huh7 cells and HepG2.2.15 cells treated with 64 μmol/L and 1 024 μmol/L Mn2+ solution (respectively) were significantly different (all P<0.01), and the apoptosis rates increased with the increase of Mn2+ concentration. Conclusion Mn2+ can inhibit the proliferation and colony formation of liver cancer cells and induce apoptosis.

Key words: Liver cancer')">Liver cancer, Manganese ion, Cell proliferation, Cell apoptosis

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  • 引用本文

    贺紫云, 王昊伦, 范倩青, 刘志辉. 锰离子对肝癌细胞增殖及凋亡的影响[J]. 中国癌症防治杂志, 2024, 16(1): 62-66.

    HE Ziyun, WANG Haolun, FAN Qianqing, LIU Zhihui . Effects of manganese ion on proliferation and apoptosis of  liver cancer cells[J]. Chinese Journal of Oncology Prevention and Treatment, 2024, 16(1): 62-66.