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分泌肿瘤坏死因子的基因工程细胞对HepG2细胞的抑制作用
引用本文:高宇红,薛毅珑. 分泌肿瘤坏死因子的基因工程细胞对HepG2细胞的抑制作用[J]. 肿瘤防治研究, 2012, 39(8): 944-946. DOI: 10.3971/j.issn.1000-8578.2012.08.015
作者姓名:高宇红  薛毅珑
作者单位:100853北京,解放军总医院南楼老年医学研究所细胞生物学研究室
摘    要:目的自行建立分泌人肿瘤坏死因子α的基因工程细胞,将其与肝癌细胞共培养,观察体外培养中分泌肿瘤坏死因子hTNF/293基因细胞表达的情况及对人肝癌细胞的抑制作用。方法(1)建立可稳定分泌人肿瘤坏死因子α/293细胞;采用RT-PCR、Western blot、ELISA和流式细胞仪等技术检测人肿瘤坏死因子表达和分泌;(2)观察体外培养中分泌肿瘤坏死因子hTNF/293基因细胞对人肝癌细胞的抑制作用,于不同的时间点,用MTT法检测490 nm下的吸光度值。结果RT-PCR、Western blot和ELISA等技术检测表明hTNFα/293 细胞组和TNFα阳性组对共培养的HepG2细胞的增殖具有明显的抑制作用,且具有良好的量效关系。结论提示TNF-α/293基因细胞可有效分泌hTNFα蛋白,并能分泌到细胞外;体外培养的人肿瘤坏死因子基因的工程细胞,所分泌肿瘤坏死因子α对人肝癌细胞增殖有明显抑制效应,且呈现出良好的数量依赖关系。

关 键 词:人肝癌细胞HepG2  人肿瘤坏死因子&alpha  人胚胎肾细胞-293  
收稿时间:2011-11-24;

Inhibitory Effects on HepG2 Cells from Genetic Engineering Cells Secreted Tumor Necrosis Factor
Gao Yuhong , Xue Yilong. Inhibitory Effects on HepG2 Cells from Genetic Engineering Cells Secreted Tumor Necrosis Factor[J]. Cancer Research on Prevention and Treatment, 2012, 39(8): 944-946. DOI: 10.3971/j.issn.1000-8578.2012.08.015
Authors:Gao Yuhong    Xue Yilong
Affiliation:Department of Cytobiology Laboratory,Gerontology Institute,PLA General Hospital,Beijing 100853,China
Abstract:Objective To explore the effects of genetic engineering cells which secreted tumor necrosis factor(TNFα) co-cultured with human hepatic cancer cells HepG2 on the proliferation of cancer cells.Methods The expression and secreting of tumor necrosis factor was detected by RT-PCR,Western blot,ELISA and flow cytometry from the 293 cells which could stably secrete TNF-α.The inhibitory effects on the hepatic cancer cells HepG2 from the 293 cells(hTNFα/293) were detected by MTT assay under the wavenumber of 490 nm at different time.Results The results from RT-PCR,Western blot and ELISA indicated that hTNF-α/293 cells and TNF-α-positive group had significant inhibition on the proliferation of hepatic cancer cells in a dose-dependent manner.Conclusion The TNF-α/293 cells can effectively secrete TNF-α.And the TNF-α secreted from the genetic engineering cells has an inhibition on hepatic cancer cell proliferation in a dose-dependent manner.
Keywords:HepG2 cells  Human tumor necrosis factor-α  Human embryonic kidney cell-293
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