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TPA对人食管癌Eca109细胞增殖和细胞核形态的影响

作者:郭玉忠，贾琳静，郜娜，田鑫，谢敏，张莉蓉，乔海灵整理:无忧论文网录入时间：[07-04-03 13:40:34] 浏览点击数:

【摘要】目的研究佛波酯 (12-O-tetradecanoylphorbol-13-acetate，TPA) 对人食管癌细胞的影响。方法细胞增殖试验采用MTT法和细胞计数的方法，细胞核形态的测量采用计算机辅助的图像分析系统，分别测量计算细胞核面积(NA)、核周长(NP)、最大直径(Dmax)、最小直径(Dmin)、核浆比(NPA)、核轴比(NAR)、核形状因子(NRF)等。结果 TPA没有抑制人食管癌Eca109细胞增殖和改变细胞核形态。结论 TPA对人食管癌Eca109细胞可能没有促分化作用。

    【关键词】佛波酯；食管癌细胞；细胞核形态

    Effects of TPA on proliferation and nuclear morphometry of human esophageal cancer Eca109 cells

    【Abstract】 Objectives To investigate the effects of 12-O-tetradecanoy lphorbol-13-acetate (TPA) on human esophageal cancer Eca109 cells. Methods The sensitivity of TPA to Eca109 cells was determined with MTT assay and counting cell numbers. After the cells were stained with HE，the measurements of nuclear morphometry were performed with computer-assisted image analysis system. Results TPA did not inhibit the cells proliferation and decrease the nuclear size. Conclusions TPA may not induce Eca109 cells to differentiate.

    【Key words】 12-O-tetradecanoylphorbol-13-acetate (TPA)；esophageal cancer cell line；nuclear morphometry

    Human esophageal cancer is one of the most common solid tumors in China. Due to its high metastatic potential and the frequent onset of resistance to chemotherapy，it is one of the major causes of death by neoplasia in the country. The present chemotherapy of cancer uses agents that are usually toxic to normal cells. On the other hand，induction of cellular differentiation may supplement the use of non-cytotoxic drugs in several forms of neoplasia，like the successful use of all-transretinoic acid (ATRA) in the treatment of acute promyelocytic leukemia.

    Plant diterpine phorbol esters，particularly the phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA)，are among the most potent tumor promoters known and their effects range from stimulating DNA synthesis through activating gene expression to producing alterations in membrane properties and constituents. TPA can also potentiate the differentiation of various tumor cells in culture and in vivo of human beings. TPA can induce differentiation and inhibit the growth of a number of malignant cell types，including myeloid leukemia［1］，breast［2］，prostate［3］，colon［4］，and brain［5］. Other report showed that TPA could not induce human hepatoca


    rcinoma cell line to differentiation［6］. Because of its efficiency in vivo［7］，we are interested in its effects on human esophageal cancer cells. Here，we report the effects of TPA on proliferation and nuclear morphometry of human esophageal cancer Eca109 cells.

    1 Materials and methods

    1.1 Chemicals TPA purchased from Sigma Chemical Co. was dissolved in ethanol and stored at -20℃.The stock solutions were diluted with Hanks’ buffered salt solution. The final concentration of ethanol in the incubation mixtures was 0.1% or less.

    1.2 Cell Growth Studies Human esophageal cancer cell line Eca109 was kindly provided by professor Bai jingxiu，Zhengzhou University. The cells were maintained in RPMI 1640 medium with 10% fetal bovine serum (FBS) in the presence of antibiotics，penicillin (100 units/ml)and streptomycin (100units/ml). All cells were cultured at 37℃ in a humidified atmosphere containing 5% CO2. The medium was replaced after 3 days. The cells were routinely subcultured twice a week.

    Cells were plated in either flasks (25cm2) or 96-well plates. TPA was added 24 hours after seeding，when the cells were attached to the surface of the containers. An equivalent volume of ethanol was added to the controls and had no effect on growth. After removing the cells from the flasks by trypsinization they were counted using a hemocytometer，fixed with 70% ethanol and stained by H.E. When the cells were plated into a 96-well microplate，the culture medium containing different concentrations of TPA was replaced 24 hours later. After 3-5 days of incubation，cell viability was evaluated by MTT assay.

    1.3 Nuclear morphometry measurements   Measurements of nuclear morphometry including nuclear area (NA)，nuclear perimeter (NP)，maximal diameter (Dmax)，minimal diameter (Dmin)，nuclear plasma ratio (NPR)，nuclear axis ratio (NAR)，nuclear roundness factor (NRF)，were performed with computer-assisted image analysis system MPIAS-500 (QingPing Image Engineering Company，Tongji University). Two fields were selected at random from each case for the measurements. Each field was viewed under a ×100 oil-immension lens and displayed on the screen of a color video image processor. The images of 50 nuclei of the tumour cells per field were outlined with a drawing pen，and the data were processed by a computer in the system，which calculated the parameters. In the end all the mean values of each case were calculated.

    1.4 Statistical Analysis The data were expressed as means±SD. Statistical analysis was performed by SPSS 10.0 software. The criterion for statistical significance was taken as P <0.05.

    2 Results

    Effect of TPA on cell Growth. The growth of Eca109 cells was not arrested by TPA at non cytotoxic concentrations. As shown in Table 1 and Fig.1，TPA even increased the cancer cell numbers，though there were no significance between TPA groups and the controls.

Table 1 Cell numbers of TPA treatments onEca109 cells (x±s)

Table 1 Cell numbers of TPA treatments onEca109 cells (x±s)

Fig.1 MTT assay of TPA treatments on Eca109

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