禹名卉, 王福利, 李天然. 骨髓间充质干细胞对低转移肝癌细胞的影响[J]. 中国肿瘤临床, 2017, 44(23): 1169-1174. DOI: 10.3969/j.issn.1000-8179.2017.23.184
引用本文: 禹名卉, 王福利, 李天然. 骨髓间充质干细胞对低转移肝癌细胞的影响[J]. 中国肿瘤临床, 2017, 44(23): 1169-1174. DOI: 10.3969/j.issn.1000-8179.2017.23.184
YU Minghui, WANG Fuli, LI Tianran. Effect of bone marrow mesenchymal stem cells on low metastatic hepatocellular carcinoma cells[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2017, 44(23): 1169-1174. DOI: 10.3969/j.issn.1000-8179.2017.23.184
Citation: YU Minghui, WANG Fuli, LI Tianran. Effect of bone marrow mesenchymal stem cells on low metastatic hepatocellular carcinoma cells[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2017, 44(23): 1169-1174. DOI: 10.3969/j.issn.1000-8179.2017.23.184

骨髓间充质干细胞对低转移肝癌细胞的影响

Effect of bone marrow mesenchymal stem cells on low metastatic hepatocellular carcinoma cells

  • 摘要:
      目的   观察人骨髓间充质干细胞(bone marrow mesenchymal stem cells, BMSCs)对植入低转移肝癌细胞动物模型生长的影响情况以及对转移潜能和凋亡趋势的影响。
      方法  制作人低转移肝癌细胞MHCC97-L动物模型, 将动物随机分为模型实验组、对照组。实验组在接种肿瘤后第7 d开始尾静脉注射BMSCs 5×105/只, 模型对照组相同时间尾静脉注射BMSCs培养液0.2 mL/只。于实验开始后每周用卡尺测一次皮下肿瘤体积, 分别于肿瘤接种后第14d(2周)、21 d(3周)、28 d(4周)、35 d(5周)、42 d(6周)处死动物, 完整剖取瘤块并称瘤重和体积, 计算肿瘤抑制率。Real-time PCR法检测低转移肝癌动物模型标本中转移相关因子骨桥蛋白(osteopontin, OPN)、骨唾液蛋白(bone salivary protein, BSP)、整合素(integrinαⅤ)基因以及凋亡相关因子Bcl-2、Bax、caspase3基因的表达。
      结果  骨髓间充质干细胞对肿瘤重量和体积的抑制作用在第3周具有统计学意义, 实验组肿瘤重量显著低于对照组。骨髓间充质干细胞对肿瘤的抑制作用在第2、3、5、6周均具有统计学意义, 实验组肿瘤体积显著低于对照组。实验组肿瘤转移相关因子表达均低于对照组, 骨髓间充质干细胞干预后肿瘤促凋亡因子Bax、caspase3的表达呈升高趋势, 抗凋亡因子Bcl-2的表达逐渐下降。
      结论  骨髓间充质干细胞对低转移肝癌细胞MHCC97-L的生长具有抑制作用, 且第3周时抑制效果最好, 随着时间的延长, 肿瘤抑制率逐渐下降。

     

    Abstract:
      Objective  To observe the effect of human bone marrow mesenchymal stem cells(BMSCs) on the growth, metastasis and apoptosis of hepatocarcinoma cells with low metastatic potential.
      Methods  Mouse model with low metastatic liver cancer cells were used.Mice were randomly divided into the model experimental group and the control group.In the experimental group, BMSCs(5 × 105) were injected into the tail vein of each mouse on the 7th day after inoculation with hepatocarcinoma cells.Mice in the control group were injected with the culture solution(0.2 mL per mouse) of BMSCs through the tail vein at the same time.The subcutaneous tumor volume was measured every week after the start of the experiment.Animals were sacrificed at day 14(2 weeks), day 21(3 weeks), day 28(4 weeks), day 35(5 weeks), and day 42(6 weeks) after inoculation of tumor cells.Complete dissection of the tumor blocks was done and the tumor inhibition rate was calculated by weight and volume.Real-time PCR was used to detect the expression of the osteopontin, bone salivary protein, and integrinαⅤgenes and the expression of Bcl-2, Bax, and caspase3 genes.
      Results  The inhibitory effect of BMSCs on tumor weight was statistically significant at 3 weeks.The tumor weight of the samples from the experimental group was significantly lower than that of the samples from control group.The inhibitory effect of BMSCs on tumor volume was statistically significant at 2, 3, 5, and 6 weeks.The tumor volume of the samples from the experimental group was significantly lower than that of the samples from the control group.The expression of pro-apoptotic factors, Bax and caspase3, in BMSCs was increased, and the expression of anti-apoptotic factor, Bcl-2, decreased gradually.
      Conclusion  BMSCs inhibited the growth of low metastatic hepatocellular carcinoma cells.The inhibition rate on tumor weight and volume was highest at the third week, and the tumor inhibition rate decreased gradually with time.

     

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