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本文引用的文献

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MicroRNAs in Cancer.癌症中的微小RNA
Annu Rev Med. 2009;60:167-79. doi: 10.1146/annurev.med.59.053006.104707.
2
MicroRNA-23b cluster microRNAs regulate transforming growth factor-beta/bone morphogenetic protein signaling and liver stem cell differentiation by targeting Smads.微小RNA-23b簇微小RNA通过靶向Smads调节转化生长因子-β/骨形态发生蛋白信号通路及肝干细胞分化。
Hepatology. 2009 Aug;50(2):575-84. doi: 10.1002/hep.22982.
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Anchorage-independent cell growth signature identifies tumors with metastatic potential.不依赖贴壁的细胞生长特征可识别具有转移潜能的肿瘤。
Oncogene. 2009 Aug 6;28(31):2796-805. doi: 10.1038/onc.2009.139. Epub 2009 Jun 1.
4
c-Myc suppression of miR-23a/b enhances mitochondrial glutaminase expression and glutamine metabolism.c-Myc对miR-23a/b的抑制作用增强了线粒体谷氨酰胺酶的表达及谷氨酰胺代谢。
Nature. 2009 Apr 9;458(7239):762-5. doi: 10.1038/nature07823. Epub 2009 Feb 15.
5
Lin-28B transactivation is necessary for Myc-mediated let-7 repression and proliferation.Lin-28B反式激活对于Myc介导的let-7抑制和增殖是必需的。
Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3384-9. doi: 10.1073/pnas.0808300106. Epub 2009 Feb 11.
6
Distinct thresholds govern Myc's biological output in vivo.不同的阈值在体内调控Myc的生物学效应。
Cancer Cell. 2008 Dec 9;14(6):447-57. doi: 10.1016/j.ccr.2008.10.018.
7
Reflecting on 25 years with MYC.回顾与MYC相伴的25年。
Nat Rev Cancer. 2008 Dec;8(12):976-90. doi: 10.1038/nrc2231.
8
Emerging role of miR-106b-25/miR-17-92 clusters in the control of transforming growth factor beta signaling.miR-106b-25/miR-17-92簇在转化生长因子β信号调控中的新作用
Cancer Res. 2008 Oct 15;68(20):8191-4. doi: 10.1158/0008-5472.CAN-08-1768.
9
miR-17 and miR-20a temper an E2F1-induced G1 checkpoint to regulate cell cycle progression.微小RNA-17和微小RNA-20a调节由E2F1诱导的G1期检查点,以调控细胞周期进程。
Oncogene. 2009 Jan 8;28(1):140-5. doi: 10.1038/onc.2008.372. Epub 2008 Oct 6.
10
Global regulation of nucleotide biosynthetic genes by c-Myc.c-Myc对核苷酸生物合成基因的全局调控
PLoS One. 2008 Jul 16;3(7):e2722. doi: 10.1371/journal.pone.0002722.

Myc 诱导的 microRNAs 整合了 Myc 介导的细胞增殖和细胞命运。

Myc-induced microRNAs integrate Myc-mediated cell proliferation and cell fate.

机构信息

Duke Institute for Genome Sciences & Policy, Duke University Medical Center, Durham, North Carolina, USA.

出版信息

Cancer Res. 2010 Jun 15;70(12):4820-8. doi: 10.1158/0008-5472.CAN-10-0659. Epub 2010 Jun 1.

DOI:10.1158/0008-5472.CAN-10-0659
PMID:20516112
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2888768/
Abstract

The Myc pathway, often deregulated in cancer, is critical in determining cell fate by coordinating a gene expression program that links the control of cell proliferation with cell fate decisions. As such, precise control of the Myc pathway activity must be achieved to ensure faithful execution of appropriate cellular response and to prevent progressing toward a malignant state. With recent highlighted roles of microRNAs (miRNA) as critical components of gene control, we sought to evaluate the extent to which miRNAs may contribute in the execution of Myc function. Combined analysis of mRNA and miRNA expression profiles reveals an integration whereby the Myc-mediated induction of miRNAs leads to the repression of various mRNAs encoding tumor suppressors that block cell proliferation including p21, p27, and Rb. In addition, the proapoptotic PTEN tumor suppressor gene is also repressed by Myc-induced miRNAs, suggesting that Myc-induced miRNAs contribute to the precise control of a transcriptional program that coordinates the balance of cell proliferation and cell death.

摘要

Myc 通路在癌症中经常失调,通过协调一个基因表达程序,将细胞增殖的控制与细胞命运决定联系起来,从而对细胞命运起着决定性作用。因此,必须精确控制 Myc 通路的活性,以确保细胞能够执行适当的反应,防止向恶性状态发展。鉴于 microRNAs(miRNA)作为基因调控关键成分的最新突出作用,我们试图评估 miRNA 在执行 Myc 功能方面可能起到的作用。mRNA 和 miRNA 表达谱的综合分析揭示了一种整合方式,即 Myc 介导的 miRNA 诱导导致各种编码肿瘤抑制因子的 mRNA 被抑制,这些抑制因子阻止细胞增殖,包括 p21、p27 和 Rb。此外,促凋亡的 PTEN 肿瘤抑制基因也被 Myc 诱导的 miRNA 抑制,这表明 Myc 诱导的 miRNA 有助于精确控制协调细胞增殖和细胞死亡平衡的转录程序。