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如何抑制端粒酶活性以用于癌症治疗。

How to inhibit telomerase activity for cancer therapy.

作者信息

Kyo Satoru, Inoue Masaki

机构信息

Department of Obstetrics and Gynecology, Kanazawa University, School of Medicine, 13-1, Takaramachi, Kanazawa, Ishikawa 920-8641, Japan.

出版信息

Curr Med Chem Anticancer Agents. 2002 Sep;2(5):613-26. doi: 10.2174/1568011023353796.

Abstract

Telomerase is a target for anticancer research because telomerase activity is closely correlated with malignancy. Inhibition of telomerase activity should increase telomere shortening, which destabilizes chromosomes, thus leading to cellular senescence and death. Extensive investigations have addressed the molecular mechanisms of telomerase activation in cancers. Based on results from these studies, various attempts have been made to inhibit telomerase activity using molecular techniques in cancer cells. Antisense oligonucleotides directed to human telomerase RNA, the dominant negative form of human telomerase reverse transcriptase (hTERT), hammerhead ribozymes that cut hTR and agents that interact with quadruplex DNA represent potential telomerase inhibitors. This review includes a summary of recent attempts to inhibit telomerase activity in cancer cells and a discussion of how these tools can be applied to cancer therapy, especially in combination with established anti-cancer agents.

摘要

端粒酶是抗癌研究的一个靶点,因为端粒酶活性与恶性肿瘤密切相关。抑制端粒酶活性应会增加端粒缩短,这会使染色体不稳定,从而导致细胞衰老和死亡。广泛的研究探讨了癌症中端粒酶激活的分子机制。基于这些研究结果,人们尝试了多种利用分子技术在癌细胞中抑制端粒酶活性的方法。针对人端粒酶RNA的反义寡核苷酸、人端粒酶逆转录酶(hTERT)的显性负性形式、切割hTR的锤头状核酶以及与四链体DNA相互作用的试剂都代表了潜在的端粒酶抑制剂。这篇综述总结了近期在癌细胞中抑制端粒酶活性的尝试,并讨论了这些工具如何应用于癌症治疗,特别是与已有的抗癌药物联合使用。

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