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余红平, 仇小强, 曾小云, 钟秋安, 卢栋, 李永华. 赛莱西布对肝癌HepG2细胞增殖与凋亡影响[J]. 中国公共卫生, 2007, 23(1): 49-51. DOI: 10.11847/zgggws2007-23-01-29
引用本文: 余红平, 仇小强, 曾小云, 钟秋安, 卢栋, 李永华. 赛莱西布对肝癌HepG2细胞增殖与凋亡影响[J]. 中国公共卫生, 2007, 23(1): 49-51. DOI: 10.11847/zgggws2007-23-01-29
YU Hong-ping, CHOU Xiao-qiang, ZENG Xiao-yun, . Effects of cyclooxygenase-2 on proliferation and apoptosis in HepG2 cells[J]. Chinese Journal of Public Health, 2007, 23(1): 49-51. DOI: 10.11847/zgggws2007-23-01-29
Citation: YU Hong-ping, CHOU Xiao-qiang, ZENG Xiao-yun, . Effects of cyclooxygenase-2 on proliferation and apoptosis in HepG2 cells[J]. Chinese Journal of Public Health, 2007, 23(1): 49-51. DOI: 10.11847/zgggws2007-23-01-29

赛莱西布对肝癌HepG2细胞增殖与凋亡影响

Effects of cyclooxygenase-2 on proliferation and apoptosis in HepG2 cells

  • 摘要: 目的探讨选择性环氧合酶-2(cox-2)抑制剂赛莱西布(celecoxib)对人肝癌细胞株HepG2细胞增殖、凋亡的影响及其可能的作用机制。方法用不同浓度的赛来西布处理HepG2细胞,分别应用四甲基偶氮噻唑蓝试验、DNA梯度电泳法、放射免疫法检测赛亚西布对HepG2细胞增殖和凋亡及其cox-2活性的影响;应用免疫印迹法和比色法检测赛莱西布对HepG2细胞胱氨酸蛋白酶3(clasepase-3)蛋白质的表达及活性的影响。结果12.5,25,50μmol/L的赛莱西布作用于HepG2细胞后,HepG2细胞增殖受抑制,与对照组比较,差异有统计学意义(P<0.01);赛莱西布干预组HepG2细胞DNA明显降解,可见细胞凋亡特征性梯状DNA条带;干预组HepG2细胞caspase3蛋白表达及活性均明显升高,与对照组比较,差异均有统计学意义(P<0.01);赛莱西布明显抑制HepG2细胞cox-2活性,与对照组比较,差异有统计学意义(P<0.01)。结论赛莱西布可通过cox-2通路和caspase3通路抑制HepG2细胞增殖并诱导其凋亡。

     

    Abstract: ObjectiveTo examine the effects of a selective inhibitor of cox-2,celecoxib on growth and apoptosis in Hep G2 cells.MethodHep G2 cells were treated with various concentrations of celecoxib.Cell growth was measured by M TT,apoptosis was detected by DNA fragmentation assay,and cox-2 activity was measured by RIA;Expression of caspase-3 protein in Hep G2 cells was determined by western blot,and caspase-3 activity was measured using colorimetric assay.ResultsAfter Hep G2 cells were treated with different concentrations of celecoxib(12.5,25,50μmol/L),celecoxib could significantly suppress the growth of Hep G2 cells respectively compared with the control group(P<0.01),and celecoxib-treated Hep G2 cells produced a distinct oligosomal ladder,the characteristics of cells undergoing apoptosis;Meanwhile,The caspas-3 expression and activity of celecoxib treated Hep G2 cells were increased respectively as compared with the control groups(P<0.01).Furthermore,the level of cox-2 activity was reduced in celecoxib-treated Hep G2 cells respectively compared with the control group(P<0.01).ConclusionCelecoxib could inhibit the proliferation and increase apoptosis in Hep G2 cells by cox-2 and caspase3 pathways.

     

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