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Study of apoptosis induced by nordihydroguaiaretic acid in human ma-lignant glioma cell line SHG-44
作者姓名:郭德玉  陈意生  卞修武  史景泉  陈自强
作者单位:InstituteofPathology,SouthwestHospital,ThirdMilitaryMedicalUniversity,Chongqing400038,China
基金项目:National Natural Science Foundation of China (No. 39670296)
摘    要:Objective: To investigate the effect and mechanism of nordihydroguaiaretic acid (NDGA) on apop-tosis in human malignant glioma cell line SHG-44. Methods: Cell growth inhibition was measured with MTT assay. Cell apoptosis was observed with light and electron microscopy and TUNEL. Expression of bcl-2 gene was measured with immunohistochemistry, in situ hybridization and image analyses. Results: NDGA at the concentration of 100 μmol/L inhibited the proliferation of SHG-44 cells and induced apoptosis in a time-de-pendent manner. The expression of Bcl-2 protein in SHG-44 cells was decreased in the present of 100 μmol/L NDGA along with the duration of treatment in a negative correlation with the degree of cell apoptosis. The bcl-2 mRNA expressed in SHG-44 cells was reduced after treatment with 100 μmol/L NDGA, apparently consistent with the immunohistochemical results. Conclusion.- NDGA can induce apoptosis of human malig-nant glioma cells probably by down-regulating expression of bcl-2 gene, though the exact mechanism needs further study.

关 键 词:细胞凋亡  bcl-2  基因表达  SHG-44  神经胶质细胞  正二氢愈创酸

Study of apoptosis induced by nordihydroguaiaretic acid in human malignant glioma cell line SHG-44
GUO De-yu,CHEN Yi-sheng,BIAN Xiu-wu,SHI Jing-quan,CHEN Zi-qiang.Study of apoptosis induced by nordihydroguaiaretic acid in human ma-lignant glioma cell line SHG-44[J].Journal of Medical Colleges of PLA(China),2002,17(4):247-250,259.
Authors:GUO De-yu  CHEN Yi-sheng  BIAN Xiu-wu  SHI Jing-quan  CHEN Zi-qiang
Abstract:Objective:To investigate the effect and mechanism of nordihydroguaiaretic acid (NDGA) on apoptosis in human malignant glioma cell line SHG-44. Methods: Cell growth inhibition was measured with MTT assay. Cell apoptosis was observed with light and electron microscopy and TUNEL. Expression of bcl-2 gene was measured with immunohistochemistry, in situ hybridization and image analyses. Results: NDGA at the concentration of 100 μmol/L inhibited the proliferation of SHG-44 cells and induced apoptosis in a time-dependent manner. The expression of Bcl-2 protein in SHG-44 cells was decreased in the present of 100 μmol/L NDGA along with the duration of treatment in a negative correlation with the degree of cell apoptosis. The bcl-2 mRNA expressed in SHG-44 cells was reduced after treatment with 100 μmol/L NDGA, apparently consistent with the immunohistochemical results. Conclusion: NDGA can induce apoptosis of human malignant glioma cells probably by down-regulating expression of bcl-2 gene, though the exact mechanism needs further study.
Keywords:glioma  nordihydroguaiaretic acid  apoptosis  bcl-2
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