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Antiproliferative Effect of the Isoquinoline Alkaloid Papaverine in Hepatocarcinoma HepG-2 Cells - Inhibition of Telomerase and Induction of Senescence

机译:异喹啉生物碱罂粟碱对肝癌HepG-2细胞的抗增殖作用-端粒酶的抑制和衰老的诱导

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摘要

Cancer cells are often immortal through up-regulation of the hTERT gene, which encodes the catalytic subunit of a special reverse transcriptase to overcome end-replication problem of chromosomes. This study demonstrates that papaverine, an isoquinoline alkaloid from the Papaveraceae, can overcome telomerase dependent immortality of HepG-2 cells that was used as a model of hepatocarcinoma. Although this alkaloid does not directly interact with telomeric sequences, papaverine inhibits telomerase through down-regulation of hTERT, which was analysed using thermal FRET and qRT-PCR, respectively. The IC50 values for the reduction of both telomerase activity and hTERT expression was 60 mu M, while IC50 for cytotoxicity was 120 mu M. Repeated treatments of the cells with very low non-toxic concentrations of papaverine resulted in growth arrest and strong reduction of population doublings after 40 days. This treatment induced senescent morphology in HepG-2 cells, which was evaluated by beta-galactosidase staining. Altogether, papaverine can be regarded as a promising model compound for drug design targeting cancer development.
机译:癌细胞通常通过上调hTERT基因而永生,hTERT基因编码特殊逆转录酶的催化亚基,以克服染色体的末端复制问题。这项研究表明,罂粟碱(一种来自罂粟科的异喹啉碱生物碱)可以克服用作肝癌模型的HepG-2细胞端粒酶依赖性的永生性。尽管该生物碱不直接与端粒序列相互作用,但罂粟碱通过下调hTERT抑制端粒酶,分别使用热FRET和qRT-PCR进行了分析。端粒酶活性和hTERT表达降低的IC50值为60μM,而细胞毒性的IC50为120μM。反复用极低的无毒浓度罂粟碱处理细胞会导致生长停滞并大量减少种群40天后翻倍。该处理诱导了HepG-2细胞的衰老形态,这通过β-半乳糖苷酶染色进行了评估。总之,罂粟碱可以被视为针对癌症发展的药物设计的有希望的模型化合物。

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