YAO Sheng-tao,CHEN Jia-lin,HUANG Yi,GUO Chuan,TANG Wen-yuan.Effects of recombinant GRIM19 gene adenovirus on cell proliferation and differentiation of human glioma cell line CHG-5[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(06):548-551.
YAO Sheng-tao,CHEN Jia-lin,HUANG Yi,GUO Chuan,TANG Wen-yuan.Effects of recombinant GRIM19 gene adenovirus on cell proliferation and differentiation of human glioma cell line CHG-5[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(06):548-551.DOI:
Effects of recombinant GRIM19 gene adenovirus on cell proliferation and differentiation of human glioma cell line CHG-5
目的 观察增强外源性GRIM19(genes associated with retinoid-IFN-induced mortality 19)基因表达对恶性胶质瘤CHG-5细胞生物学特性的影响,初步探讨其机制。 方法 利用已成功构建的Ad-GRIM19腺病毒感染CHG-5细胞,通过形态学、细胞生长曲线、软琼脂克隆形成等观察增强GRIM19基因表达后CHG-5细胞形态、增殖和体外成瘤能力的变化,台盼蓝染色法检测细胞活力, Real-time PCR及Western blot 检测STAT3与PCNA基因表达。 结果 Ad-GRIM19在体外感染CHG-5细胞后,明显改变CHG-5细胞生长形态,细胞增殖及体外成瘤减低,STAT3、PCNA基因表达下调。 结论 GRIM19过表达可显著抑制CHG-5细胞恶性表型,提示GRIM19基因在调控胶质瘤细胞分化程度及恶性生物学行为方面具有重要作用。
Abstract
Objective To observe the effects of enhanced genes associated with retinoid-IFN-induced mor-tality 19 (GRIM19) expression on biological features of human malignant glioma cells in vitro. Methods Human glioma cell line CHG-5 were infected with Ad-GRIM19 and Ad-GFP (control). The infected and control glioma cells were analyzed for their morphological alterations and cell growth features by using WST-8
soft agar cloning-formation and other methods. Real-time PCR and Western blotting were employed to detect the mRNA and protein expressions of STAT3 and PCNA. Results Compared with control cells
CHG-5 cells transfected with Ad-GRIM19 demonstrated profound morphological alterations and marked cellular atypia. Cell proliferation rate and their tumorigenecity in vitro were also decreased. The mRNA and protein expressions of STAT3 and PCNA were downregulated. Conclusion Overexpression of GRIM19 gene has affected CHG-5 glioma cell morphology and decreased their growth and tumorigenecity
suggesting GRIM19 gene might play a key role in determining differentiation and certain malignant biological features of glioma cells.