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As2 O3对人胃癌BGC-823 细胞端粒酶的影响[J]. 肿瘤防治研究, 2007, 34(12): 927-931. DOI: 10.3971/j.issn.1000-8578.59
引用本文: As2 O3对人胃癌BGC-823 细胞端粒酶的影响[J]. 肿瘤防治研究, 2007, 34(12): 927-931. DOI: 10.3971/j.issn.1000-8578.59
Effects of Arsenic Trioxide ( As2 O3 ) on Telomerase Activity of Human Gastric Cancer BGC-823 Cell Line[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 927-931. DOI: 10.3971/j.issn.1000-8578.59
Citation: Effects of Arsenic Trioxide ( As2 O3 ) on Telomerase Activity of Human Gastric Cancer BGC-823 Cell Line[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 927-931. DOI: 10.3971/j.issn.1000-8578.59

As2 O3对人胃癌BGC-823 细胞端粒酶的影响

Effects of Arsenic Trioxide ( As2 O3 ) on Telomerase Activity of Human Gastric Cancer BGC-823 Cell Line

  • 摘要: 目的 观察三氧化二砷(As2 O3)对人胃癌BGC-823细胞端粒酶活性及端粒酶逆转录酶基因转录的影响。方法 用不同浓度的三氧化二砷作用于人胃癌BGC-823细胞,通过MTT法测定细胞活力;流式细胞术检测细胞凋亡变化;TRAP PCR ELIsA方法检测细胞端粒酶活性的变化;RT-PCR半定量方法检测细胞端粒酶hTEI汀基因mRNA的转录水平。结果 三氧化二砷可明显抑制人胃癌BGC-823细胞的生长,诱导细胞发生凋亡,抑制作用随三氧化二砷浓度的升高及作用时间的延长而增强。细胞的端粒酶活性明显下降,细胞hTERT基因的转录表达显著抑制。BGC-823细胞端粒酶活性的下调与As2 O3作用时间和浓度有关,呈现明显的时间-剂量效应关系。结论 As2 O3能够抑制人胃癌BGC-823细胞的增殖、促使细胞凋亡、抑制细胞的端粒酶活性。As2 O3是一种良好的端粒酶抑制剂,在肿瘤的治疗中具有一定应用价值。

     

    Abstract: Objective  To evaluate telomerase activity of human gastric cancer cell Line BGC-823 cultured with different concent ration of Arsenic Trioxide and genetic t ranscription level of human telomerase reverse transcriptase (hTERT) . Methods  The cell activity of BGC-823 cells was measured using MTT method af ter BGC-823 cells cultured with various concent rations of As2 O3 . Changes in apoptosis of BGC-823 cells were analyzed with flow cytometry ( FCM) . Telomerase activity was determined by telomeric repeat amplification protocol PCR EL ISA ( TRAP PCR EL ISA) . The mRNA level of hTERT gene was tested by semi-quantitive RT-PCR. Results  The proliferation of BGC-823 cells cultured with As2 O3was significantly inhibited and result in cells apoptosis. The tendency of proliferation inhibition depended on As2 O3 dose increasing and administ rated time prolong. Meanwhile, telomerase activities were markedly decreased and genetic t ranscription expressions of hTERT were obviously suppressed. These changes also show obvious time-Dose-response relationship . Conclusion  As2 O3 could inhibit the generation of BGC-823 cells and activation of telomerase. It maybe a good telomerase inhibitor, this is value for clinical application of tumor therapy.

     

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