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锤头状核酶介导的人肝癌细胞提取物中端粒酶活性的抑制作用。

Hammerhead ribozyme-mediated inhibition of telomerase activity in extracts of human hepatocellular carcinoma cells.

作者信息

Kanazawa Y, Ohkawa K, Ueda K, Mita E, Takehara T, Sasaki Y, Kasahara A, Hayashi N

机构信息

First Department of Medicine, Osaka University School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1996 Aug 14;225(2):570-6. doi: 10.1006/bbrc.1996.1213.

Abstract

Telomerase, a ribonucleoprotein that directs the synthesis of telomeric DNA repeats and compensates for the telomeric losses that occur with cell division, is absent from most mortal cells but is present in immortal cells. Telomerase activity is thought to be essential for continuous cell division as seen in malignant tumor cells, and its inhibition could be a strategy for anti-cancer therapy. We prepared a hammerhead ribozyme (teloRZ) directed against the RNA component of human telomerase and tried to find if it could serve as an inhibitor of telomerase. TeloRZ showed a specific cleavage activity against a synthesized portion of the telomerase RNA component used as the substrate. Furthermore, when added to cell extracts from HepG2 or Huh-7, human hepatocellular carcinoma derived lines, teloRZ inhibited the telomerase activity in both. These findings support the potential application of ribozymes capable of telomerase inhibition as new therapeutic agents directed against immortalized cancer cells.

摘要

端粒酶是一种核糖核蛋白,它指导端粒DNA重复序列的合成,并补偿细胞分裂过程中发生的端粒损失。大多数正常细胞中不存在端粒酶,但在永生化细胞中存在。端粒酶活性被认为对恶性肿瘤细胞中所见的持续细胞分裂至关重要,抑制其活性可能是一种抗癌治疗策略。我们制备了一种针对人端粒酶RNA成分的锤头状核酶(teloRZ),并试图确定它是否可作为端粒酶的抑制剂。TeloRZ对用作底物的端粒酶RNA成分的合成部分表现出特异性切割活性。此外,当将其添加到源自人肝癌细胞系HepG2或Huh-7的细胞提取物中时,teloRZ抑制了两者的端粒酶活性。这些发现支持了能够抑制端粒酶的核酶作为针对永生化癌细胞的新型治疗剂的潜在应用。

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