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端粒缩短使癌细胞对选定的细胞毒性药物敏感:体外和体内研究及推测的机制。

Telomere shortening sensitizes cancer cells to selected cytotoxic agents: in vitro and in vivo studies and putative mechanisms.

机构信息

Beilinson Hospital, Rabin Medical Center, Felsenstein Medical Research Center, Petah-Tikva, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

出版信息

PLoS One. 2010 Feb 9;5(2):e9132. doi: 10.1371/journal.pone.0009132.

Abstract

BACKGROUND

Telomere/telomerase system has been recently recognized as an attractive target for anticancer therapy. Telomerase inhibition results in tumor regression and increased sensitivity to various cytotoxic drugs. However, it has not been fully established yet whether the mediator of these effects is telomerase inhibition per se or telomere shortening resulting from inhibition of telomerase activity. In addition, the characteristics and mechanisms of sensitization to cytotoxic drugs caused by telomerase inhibition has not been elucidated in a systematic manner.

METHODOLOGY/PRINCIPAL FINDINGS: In this study we characterized the relative importance of telomerase inhibition versus telomere shortening in cancer cells. Sensitization of cancer cells to cytotoxic drugs was achieved by telomere shortening in a length dependent manner and not by telomerase inhibition per se. In our system this sensitization was related to the mechanism of action of the cytotoxic drug. In addition, telomere shortening affected also other cancer cell functions such as migration. Telomere shortening induced DNA damage whose repair was impaired after administration of cisplatinum while doxorubicin or vincristine did not affect the DNA repair. These findings were verified also in in vivo mouse model. The putative explanation underlying the phenotype induced by telomere shortening may be related to changes in expression of various microRNAs triggered by telomere shortening.

CONCLUSIONS/SIGNIFICANCE: To our best knowledge this is the first study characterizing the relative impact of telomerase inhibition and telomere shortening on several aspects of cancer cell phenotype, especially related to sensitivity to cytotoxic drugs and its putative mechanisms. The microRNA changes in cancer cells upon telomere shortening are novel information. These findings may facilitate the development of telomere based approaches in treatment of cancer.

摘要

背景

端粒/端粒酶系统最近被认为是一种有吸引力的抗癌治疗靶点。端粒酶抑制导致肿瘤消退和增加对各种细胞毒性药物的敏感性。然而,尚未完全确定这些作用的介导物是端粒酶抑制本身还是端粒酶活性抑制导致的端粒缩短。此外,端粒酶抑制引起的细胞毒性药物敏感性的特征和机制尚未系统阐明。

方法/主要发现:在这项研究中,我们对癌细胞中端粒酶抑制与端粒缩短的相对重要性进行了表征。通过端粒缩短以长度依赖的方式而非端粒酶抑制本身使癌细胞对细胞毒性药物敏感。在我们的系统中,这种敏感性与细胞毒性药物的作用机制有关。此外,端粒缩短还影响了其他癌细胞功能,如迁移。端粒缩短诱导的 DNA 损伤,在顺铂给药后其修复受损,而阿霉素或长春新碱则不影响 DNA 修复。这些发现也在体内小鼠模型中得到了验证。端粒缩短诱导的表型的潜在解释可能与端粒缩短引发的各种 microRNA 表达变化有关。

结论/意义:据我们所知,这是首次研究端粒酶抑制和端粒缩短对癌细胞表型的几个方面的相对影响的研究,特别是与细胞毒性药物敏感性及其潜在机制有关。端粒缩短后癌细胞中 microRNA 的变化是新的信息。这些发现可能有助于基于端粒的方法在癌症治疗中的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec78/2817744/79912aa56abd/pone.0009132.g001.jpg

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