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本文引用的文献

1
Negative regulation of tumor suppressor p53 by microRNA miR-504.肿瘤抑制因子 p53 受 microRNA miR-504 的负调控。
Mol Cell. 2010 Jun 11;38(5):689-99. doi: 10.1016/j.molcel.2010.05.027.
2
The regulation of energy metabolism and the IGF-1/mTOR pathways by the p53 protein.p53 蛋白对能量代谢和 IGF-1/mTOR 通路的调节作用。
Trends Cell Biol. 2010 Jul;20(7):427-34. doi: 10.1016/j.tcb.2010.03.004.
3
Glutaminase 2, a novel p53 target gene regulating energy metabolism and antioxidant function.谷氨酰胺酶 2:一种新的 p53 靶基因,调节能量代谢和抗氧化功能。
Proc Natl Acad Sci U S A. 2010 Apr 20;107(16):7455-60. doi: 10.1073/pnas.1001006107. Epub 2010 Apr 8.
4
P53-induced microRNA-107 inhibits HIF-1 and tumor angiogenesis.P53 诱导的 microRNA-107 抑制 HIF-1 和肿瘤血管生成。
Proc Natl Acad Sci U S A. 2010 Apr 6;107(14):6334-9. doi: 10.1073/pnas.0911082107. Epub 2010 Mar 22.
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MicroRNA control of signal transduction.微小 RNA 对信号转导的调控。
Nat Rev Mol Cell Biol. 2010 Apr;11(4):252-63. doi: 10.1038/nrm2868. Epub 2010 Mar 10.
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Genetic dissection of the miR-17~92 cluster of microRNAs in Myc-induced B-cell lymphomas.Myc诱导的B细胞淋巴瘤中微小RNA的miR-17~92簇的遗传学剖析
Genes Dev. 2009 Dec 15;23(24):2806-11. doi: 10.1101/gad.1872909.
7
RETRACTED: miR-221&222 regulate TRAIL resistance and enhance tumorigenicity through PTEN and TIMP3 downregulation.撤回:miR-221和miR-222通过下调PTEN和TIMP3来调节TRAIL抗性并增强肿瘤发生能力。
Cancer Cell. 2009 Dec 8;16(6):498-509. doi: 10.1016/j.ccr.2009.10.014.
8
MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression.在结直肠腺瘤向腺癌进展过程中,miR-17-92簇与13q增益及c-myc表达相关。
Br J Cancer. 2009 Aug 18;101(4):707-14. doi: 10.1038/sj.bjc.6605037.
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Modulation of microRNA processing by p53.p53对微小RNA加工的调控
Nature. 2009 Jul 23;460(7254):529-33. doi: 10.1038/nature08199.
10
MiR-122/cyclin G1 interaction modulates p53 activity and affects doxorubicin sensitivity of human hepatocarcinoma cells.微小RNA-122/细胞周期蛋白G1相互作用调节p53活性并影响人肝癌细胞对阿霉素的敏感性。
Cancer Res. 2009 Jul 15;69(14):5761-7. doi: 10.1158/0008-5472.CAN-08-4797. Epub 2009 Jul 7.

肿瘤抑制因子 p53 与 microRNAs 的相遇。

Tumor suppressor p53 meets microRNAs.

机构信息

Department of Radiation Oncology, Cancer Institute of New Jersey, University of Medicine and Dentistry of New Jersey, New Brunswick, NJ 08903, USA.

出版信息

J Mol Cell Biol. 2011 Feb;3(1):44-50. doi: 10.1093/jmcb/mjq040.

DOI:10.1093/jmcb/mjq040
PMID:21278451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3030969/
Abstract

Tumor suppressor p53 plays a central role in tumor prevention. As a transcription factor, p53 mainly exerts its function through transcription regulation of its target genes to initiate various cellular responses. To maintain its proper function, p53 is tightly regulated by a wide variety of regulators in cells. Thus, p53, its regulators and regulated genes form a complex p53 network which is composed of hundreds of genes and their products. microRNAs (miRNAs) are a class of endogenously expressed, small non-coding RNA molecules which play a key role in regulation of gene expression at the post-transcriptional level. Recent studies have demonstrated that miRNAs interact with p53 and its network at multiple levels. p53 regulates the transcription expression and the maturation of a group of miRNAs. On the other hand, miRNAs can regulate the activity and function of p53 through direct repression of p53 or its regulators in cells. These findings have demonstrated that miRNAs are important components in the p53 network, and also added another layer of complexity to the p53 network.

摘要

抑癌基因 p53 在肿瘤预防中起着核心作用。作为转录因子,p53 主要通过转录调节其靶基因来启动各种细胞反应。为了保持其适当的功能,p53 在细胞中受到多种调节因子的严格调控。因此,p53、其调节因子和受调节的基因形成了一个由数百个基因及其产物组成的复杂 p53 网络。 microRNAs (miRNAs) 是一类内源性表达的、小的非编码 RNA 分子,在转录后水平调控基因表达中起着关键作用。最近的研究表明,miRNAs 在多个层面上与 p53 及其网络相互作用。p53 调节一组 miRNAs 的转录表达和成熟。另一方面,miRNAs 可以通过直接抑制细胞中的 p53 或其调节因子来调节 p53 的活性和功能。这些发现表明,miRNAs 是 p53 网络的重要组成部分,也为 p53 网络增加了另一层复杂性。