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有丝分裂作为抗癌靶点。

Mitosis as an anti-cancer target.

机构信息

Department of Medical Oncology, Cancer Genomics Center, UMC Utrecht, The Netherlands.

出版信息

Oncogene. 2011 Jun 23;30(25):2799-809. doi: 10.1038/onc.2011.30. Epub 2011 Feb 21.

DOI:10.1038/onc.2011.30
PMID:21339734
Abstract

Most of the current drugs used to treat cancer can be classified as anti-proliferative drugs. These drugs perturb the proliferative cycle of tumor cells at diverse stages of the cell cycle. Examples of such drugs are DNA-damaging agents and inhibitors of cyclin-dependent kinases that arrest cell cycle progression at different stages of interphase. Another class of anti-proliferative drugs is the so-called anti-mitotic drugs, which selectively perturb progression through mitosis. Mitosis is the shortest and final stage in the cell cycle and has evolved to accurately divide the duplicated genome over the two daughter cells. This review deals with the different strategies that are currently considered to perturb mitotic progression in the treatment of cancer.

摘要

目前用于治疗癌症的大多数药物可分为抗增殖药物。这些药物在细胞周期的不同阶段扰乱肿瘤细胞的增殖周期。此类药物的例子有破坏 DNA 的药物和细胞周期蛋白依赖性激酶抑制剂,它们可使细胞周期在有丝分裂的不同阶段停滞。另一类抗增殖药物是所谓的有丝分裂抑制剂,它们选择性地扰乱有丝分裂的进展。有丝分裂是细胞周期中最短和最后的阶段,其进化目的是准确地将复制的基因组分配到两个子细胞中。这篇综述讨论了目前被认为用于扰乱有丝分裂进展以治疗癌症的不同策略。

相似文献

1
Mitosis as an anti-cancer target.有丝分裂作为抗癌靶点。
Oncogene. 2011 Jun 23;30(25):2799-809. doi: 10.1038/onc.2011.30. Epub 2011 Feb 21.
2
Mitotic drug targets and the development of novel anti-mitotic anticancer drugs.有丝分裂药物靶点与新型抗有丝分裂抗癌药物的研发
Drug Resist Updat. 2007 Aug-Oct;10(4-5):162-81. doi: 10.1016/j.drup.2007.06.003. Epub 2007 Jul 31.
3
Centrosomes and cancer: how cancer cells divide with too many centrosomes.中心体与癌症:癌细胞如何在拥有过多中心体的情况下进行分裂。
Cancer Metastasis Rev. 2009 Jun;28(1-2):85-98. doi: 10.1007/s10555-008-9163-6.
4
Mitotic drug targets.有丝分裂药物靶点。
J Cell Biochem. 2010 Oct 1;111(2):258-65. doi: 10.1002/jcb.22721.
5
Centrosome amplification, chromosome instability and cancer development.中心体扩增、染色体不稳定与癌症发展。
Cancer Lett. 2005 Dec 8;230(1):6-19. doi: 10.1016/j.canlet.2004.12.028.
6
If not apoptosis, then what? Treatment-induced senescence and mitotic catastrophe in tumor cells.如果不是细胞凋亡,那是什么?肿瘤细胞中的治疗诱导衰老和有丝分裂灾难。
Drug Resist Updat. 2001 Oct;4(5):303-13. doi: 10.1054/drup.2001.0213.
7
Genotoxic stress leads to centrosome amplification in breast cancer cell lines that have an inactive G1/S cell cycle checkpoint.基因毒性应激会导致在G1/S细胞周期检查点失活的乳腺癌细胞系中出现中心体扩增。
Oncogene. 2004 May 20;23(23):4068-75. doi: 10.1038/sj.onc.1207568.
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[Molecular mechanism regulating effect of anti-cancer agents].[抗癌药物调节作用的分子机制]
Gan To Kagaku Ryoho. 2009 Jan;36(1):1-5.
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Cyclins and related kinases in cancer cells.癌细胞中的细胞周期蛋白及相关激酶。
J BUON. 2007 Sep;12 Suppl 1:S45-52.
10
A brief staurosporine treatment of mitotic cells triggers premature exit from mitosis and polyploid cell formation.用星孢菌素对有丝分裂细胞进行短暂处理会引发有丝分裂的过早退出和多倍体细胞的形成。
Cancer Res. 1996 Aug 1;56(15):3551-9.

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Chromatin bridges, not micronuclei, activate cGAS after drug-induced mitotic errors in human cells.在人类细胞中,药物诱导有丝分裂错误后,染色质桥而非微核激活了cGAS。
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The phosphatase CTDSPL2 is phosphorylated in mitosis and a target for restraining tumor growth and motility in pancreatic cancer.磷酸酶 CTDSPL2 在有丝分裂中被磷酸化,是抑制胰腺癌肿瘤生长和运动的靶点。
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Playing cancer at its own game: activating mitogenic signaling as a paradoxical intervention.以其人之道还治其人之身:激活有丝分裂信号作为一种自相矛盾的干预手段。
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