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Inhibition of telomerase activity by HDV ribozyme in cancers

机译:HDV核酶对端粒酶活性的抑制作用

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Background Telomerase plays an important role in cell proliferation and carcinogenesis and is believed to be a good target for anti-cancer drugs. Elimination of template function of telomerase RNA may repress the telomerase activity. Methods A pseudo-knotted HDV ribozyme (g.RZ57) directed against the RNA component of human telomerase (hTR) was designed and synthesized. An in vitro transcription plasmid and a eukaryotic expression plasmid of ribozyme were constructed. The eukaryotic expression plasmid was induced into heptocellular carcinoma 7402 cells, colon cancer HCT116 cells and L02 hepatocytes respectively. Then we determine the cleavage activity of ribozyme against human telomerase RNA component (hTR) both in vitro and in vivo, and detect telomerase activity continuously. Results HDV ribozyme showed a specific cleavage activity against the telomerase RNA in vitro. The maximum cleavage ratio reached about 70.4%. Transfection of HDV ribozyme into 7402 cells and colon cancer cells HCT116 led to growth arrest and the spontaneous apoptosis of cells, and the telomerase activity dropped to 10% of that before. Conclussion HDV ribozyme (g.RZ57) is an effective strategy for gene therapy.
机译:背景端粒酶在细胞增殖和致癌作用中起着重要作用,并且被认为是抗癌药物的良好靶标。消除端粒酶RNA的模板功能可能会抑制端粒酶活性。方法设计并合成了针对人端粒酶(hTR)RNA成分的假结HDV核酶(g.RZ57)。构建了核酶的体外转录质粒和真核表达质粒。真核表达质粒分别被诱导入肝细胞癌7402细胞,结肠癌HCT116细胞和L02肝细胞。然后,我们确定了核酶对人端粒酶RNA组分(hTR)的体内和体外裂解活性,并连续检测端粒酶活性。结果HDV核酶在体外显示出对端粒酶RNA的特异性切割活性。最大切割率达到约70.4%。 HDV核酶转染入7402细胞和结肠癌细胞HCT116导致细胞生长停滞和细胞自发凋亡,端粒酶活性降至之前的10%。结论HDV核酶(g.RZ57)是基因治疗的有效策略。

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