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RNA调控与癌症发展。

RNA regulation and cancer development.

作者信息

Scholzová Eva, Malík Radek, Sevcík Jan, Kleibl Zdenek

机构信息

First Medical Faculty, Institute of Biochemistry and Experimental Oncology, Charles University, U Nemocnice 5, 128 53 Prague 2, Czech Republic.

出版信息

Cancer Lett. 2007 Feb 8;246(1-2):12-23. doi: 10.1016/j.canlet.2006.03.021. Epub 2006 May 3.

DOI:10.1016/j.canlet.2006.03.021
PMID:16675105
Abstract

Cancer is viewed as a genetic disease. According to the currently accepted model of carcinogenesis, several consequential mutations in oncogenes or tumor suppressor genes are necessary for cancer development. In this model, mutated DNA sequence is transcribed to mRNA that is finally translated into functionally aberrant protein. mRNA is viewed solely as an intermediate between DNA (with 'coding' potential) and protein (with 'executive' function). However, recent findings suggest that (m)RNA is actively regulated by a variety of processes including nonsense-mediated decay, alternative splicing, RNA editing or RNA interference. Moreover, RNA molecules can regulate a variety of cellular functions through interactions with RNA, DNA as well as protein molecules. Although, the precise contribution of RNA molecules by themselves and RNA-regulated processes on cancer development is currently unknown, recent data suggest their important role in carcinogenesis. Here, we summarize recent knowledge on RNA-related processes and discuss their potential role in cancer development.

摘要

癌症被视为一种基因疾病。根据目前被广泛接受的致癌模型,癌基因或肿瘤抑制基因中的多个连续性突变是癌症发生发展所必需的。在这个模型中,突变的DNA序列转录为mRNA,最终翻译为功能异常的蛋白质。mRNA仅仅被看作是DNA(具有“编码”潜能)和蛋白质(具有“执行”功能)之间的中间体。然而,最近的研究发现表明,(m)RNA受到包括无义介导的衰变、可变剪接、RNA编辑或RNA干扰等多种过程的积极调控。此外,RNA分子可以通过与RNA、DNA以及蛋白质分子的相互作用来调控多种细胞功能。尽管目前尚不清楚RNA分子本身以及RNA调控过程对癌症发生发展的确切作用,但最近的数据表明它们在致癌过程中发挥着重要作用。在此,我们总结了关于RNA相关过程的最新知识,并讨论它们在癌症发生发展中的潜在作用。

相似文献

1
RNA regulation and cancer development.RNA调控与癌症发展。
Cancer Lett. 2007 Feb 8;246(1-2):12-23. doi: 10.1016/j.canlet.2006.03.021. Epub 2006 May 3.
2
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[RNA and cancer].[RNA与癌症]
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The Role of RNA Editing in Cancer Development and Metabolic Disorders.RNA编辑在癌症发展和代谢紊乱中的作用。
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2
ADAR2/miR-589-3p axis controls glioblastoma cell migration/invasion.ADAR2/miR-589-3p 轴控制胶质母细胞瘤细胞的迁移/侵袭。
Nucleic Acids Res. 2018 Feb 28;46(4):2045-2059. doi: 10.1093/nar/gkx1257.
3
Upregulation of the MCL-1S protein variant following dihydroartemisinin treatment induces apoptosis in cholangiocarcinoma cells.
双氢青蒿素治疗后MCL-1S蛋白变体的上调诱导胆管癌细胞凋亡。
Oncol Lett. 2015 Dec;10(6):3545-3550. doi: 10.3892/ol.2015.3760. Epub 2015 Sep 29.
4
Isolation and characterization of novel RECK tumor suppressor gene splice variants.新型RECK肿瘤抑制基因剪接变体的分离与鉴定
Oncotarget. 2015 Oct 20;6(32):33120-33. doi: 10.18632/oncotarget.5305.
5
The effects of p38 gene silencing on breast cancer cells.p38基因沉默对乳腺癌细胞的影响。
Mol Biol Rep. 2014 May;41(5):2923-7. doi: 10.1007/s11033-014-3148-z. Epub 2014 Jan 28.
6
Inhibition of SMG-8, a subunit of SMG-1 kinase, ameliorates nonsense-mediated mRNA decay-exacerbated mutant phenotypes without cytotoxicity.抑制 SMG-8,一种 SMG-1 激酶的亚基,可改善无义介导的 mRNA 衰变加剧的突变表型而无细胞毒性。
Proc Natl Acad Sci U S A. 2013 Sep 10;110(37):15037-42. doi: 10.1073/pnas.1300654110. Epub 2013 Aug 27.
7
RNA editing and drug discovery for cancer therapy.用于癌症治疗的RNA编辑与药物发现。
ScientificWorldJournal. 2013 Apr 24;2013:804505. doi: 10.1155/2013/804505. Print 2013.
8
MicroRNA-mediated loss of ADAR1 in metastatic melanoma promotes tumor growth.miRNA 介导的 ADAR1 缺失促进转移性黑色素瘤的肿瘤生长。
J Clin Invest. 2013 Jun;123(6):2703-18. doi: 10.1172/JCI62980.
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Age-related prognostic impact of different types of DNMT3A mutations in adults with primary cytogenetically normal acute myeloid leukemia.成人原发性细胞遗传学正常急性髓系白血病中不同类型 DNMT3A 突变的年龄相关预后影响。
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