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首页> 外文期刊>British Journal of Cancer >Up-regulation of telomerase activity in human pancreatic cancer cells after exposure to etoposide
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Up-regulation of telomerase activity in human pancreatic cancer cells after exposure to etoposide

机译:依托泊苷暴露后人胰腺癌细胞端粒酶活性上调

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Telomerase plays a critical role in the development of cellular immortality and oncogenesis. Activation of telomerase occurs in a majority of human malignant tumours, and the relation between telomerase and vulnerability to drug-mediated apoptosis remains unclear. In this study, we demonstrate, for the first time, up-regulation of telomerase activity in human pancreatic cancer cells treated with etoposide, a topoisomerase II inhibitor. Exposure of MIA PaCa-2 cells to etoposide at various concentrations (1–30 μM) resulted in two- to threefold increases in telomerase activity. Up-regulation was detectable 24 h after drug exposure and was accompanied by enhanced expression of mRNA of the human telomerase reverse transcriptase. Telomerase activation was also observed in AsPC-1 and PANC-1 cells but not in KP-3 and KP-1N cells. Furthermore, we found a negative correlation between increased telomerase activity and the percentage of dead cells after etoposide treatment. These findings suggest the existence of an anti-apoptotic pathway through which telomerase is up-regulated in response to DNA damage. This telomerase activation pathway may be one of the mechanisms responsible for the development of etoposide resistance in certain pancreatic cancer cells. ? 2000 Cancer Research Campaign
机译:端粒酶在细胞永生和肿瘤发生发展中起关键作用。端粒酶的激活发生在大多数人类恶性肿瘤中,端粒酶与药物介导的细胞凋亡易损性之间的关系仍不清楚。在这项研究中,我们首次证明了用拓扑异构酶II抑制剂依托泊苷治疗的人胰腺癌细胞中端粒酶活性的上调。将MIA PaCa-2细胞暴露于不同浓度(1–30μM)的依托泊苷,会使端粒酶活性增加2至3倍。在药物暴露后24小时可检测到上调,并伴随着人类端粒酶逆转录酶mRNA表达的增强。在AsPC-1和PANC-1细胞中也观察到端粒酶激活,但在KP-3和KP-1N细胞中未观察到。此外,我们发现依托泊苷治疗后端粒酶活性增加与死细胞百分比之间呈负相关。这些发现表明存在抗凋亡途径,通过该途径端粒酶响应DNA损伤而被上调。该端粒酶激活途径可能是导致某些胰腺癌细胞中依托泊苷抗性发展的机制之一。 ? 2000年癌症研究运动

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