任辉, 姜涛, 房学东, 徐为然, 田宇. 苯乙酸对结直肠癌HCT-8细胞C-myc基因表达的影响[J]. 中国肿瘤临床, 2007, 34(23): 1321-1323.
引用本文: 任辉, 姜涛, 房学东, 徐为然, 田宇. 苯乙酸对结直肠癌HCT-8细胞C-myc基因表达的影响[J]. 中国肿瘤临床, 2007, 34(23): 1321-1323.
Ren Hui, Jiang Tao, Fang Xue-dong, . The Effect of Phenylacetate on C- myc Oncogene Expression in Colorectal Carcinoma Cells[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2007, 34(23): 1321-1323.
Citation: Ren Hui, Jiang Tao, Fang Xue-dong, . The Effect of Phenylacetate on C- myc Oncogene Expression in Colorectal Carcinoma Cells[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2007, 34(23): 1321-1323.

苯乙酸对结直肠癌HCT-8细胞C-myc基因表达的影响

The Effect of Phenylacetate on C- myc Oncogene Expression in Colorectal Carcinoma Cells

  • 摘要: 目的:观察诱导分化剂苯乙酸(Phenylacetate,PA)抑制结直肠癌细胞HCT-8增殖过程中C-myc基因表达的变化。方法:应用噻唑蓝(MTT)比色法,以1.0、2.0、3.0、4.0、5.0mmol/L的PA作用于HCT-8细胞,分别于24、48、72h对细胞增殖进行检测。应用原位分子杂交方法观察应用PA后对HCT-8细胞C-myc mRNA表达的情况。结果:1.0~5.0mmol/LPA作用HCT-8细胞24~72h,随着PA浓度的增加或作用时间的延长,细胞生长抑制率明显增加,PA作用24h为5.1%~24.3%,48h为16.7%~72.3%,72h为30.2%~93.4%。PA治疗后HCT-8细胞C-myc mRNA阳性表达率为(12.05±7.92)%,显著低于非治疗组中的阳性率(55.15±21.64)%(P<0.01)。结论:PA可有效抑制结直肠癌HCT-8细胞的增殖,PA对C-myc基因具有明显的抑制作用。

     

    Abstract: Objective: To observe the changes in C- myc mRNA expression in HCT- 8 colorectal carcinoma cells treated with phenylacetate (PA). Methods: HCT- 8 cells were cultured in the presence of PA at 1.0, 2.0, 3.0, 4.0, and 5.0 mmol/L. The cellular proliferation inhibitory ratio was evaluated by MTT assay 24h, 48h, and 72h later, and C- myc mRNA expression in the HCT- 8 cell line was detected by an in situ hybridization test. Results: With increased PA concentration and extended culture time, the inhibitory rate of tumor cell growth was notably increased. The inhibitory rates were 5.1%~ 24.3%,16.7%~ 72.3%, and 30.2%~ 93.4% in cells cultured for 24h, 48h, and 72h, respectively. The expression rate of C- myc was lower in cells cultured in PA than that in cells cultured without PA, with a significant difference (P<0.05). Conclusion: PA can downregulate C- myc mRNA expression and inhibit the growth of colorectal carcinoma cells.

     

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