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本文引用的文献

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MicroRNA-205 signaling regulates mammary stem cell fate and tumorigenesis.微小RNA-205信号传导调节乳腺干细胞命运和肿瘤发生。
J Clin Invest. 2014 Jul;124(7):3093-106. doi: 10.1172/JCI73351. Epub 2014 Jun 9.
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Evolution of the cancer stem cell model.癌症干细胞模型的演变。
Cell Stem Cell. 2014 Mar 6;14(3):275-91. doi: 10.1016/j.stem.2014.02.006.
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MicroRNA-542-3p inhibits tumour angiogenesis by targeting angiopoietin-2.微小 RNA-542-3p 通过靶向血管生成素-2 抑制肿瘤血管生成。
J Pathol. 2014 Apr;232(5):499-508. doi: 10.1002/path.4324. Epub 2014 Feb 24.
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Recent insights into NF-κB signalling pathways and the link between inflammation and prostate cancer.近期对核因子κB信号通路以及炎症与前列腺癌之间联系的见解。
BJU Int. 2014 Aug;114(2):168-76. doi: 10.1111/bju.12488. Epub 2014 Feb 20.
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MiR-155 promotes proliferation of human breast cancer MCF-7 cells through targeting tumor protein 53-induced nuclear protein 1.miR-155 通过靶向肿瘤抑制蛋白 53 诱导核蛋白 1 促进人乳腺癌 MCF-7 细胞的增殖。
J Biomed Sci. 2013 Oct 24;20(1):79. doi: 10.1186/1423-0127-20-79.
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MiRNA-497 regulates cell growth and invasion by targeting cyclin E1 in breast cancer.miRNA-497 通过靶向 cyclin E1 调节乳腺癌细胞的生长和侵袭。
Cancer Cell Int. 2013 Oct 10;13(1):95. doi: 10.1186/1475-2867-13-95.
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miR-720 inhibits tumor invasion and migration in breast cancer by targeting TWIST1.miR-720 通过靶向 TWIST1 抑制乳腺癌中的肿瘤侵袭和迁移。
Carcinogenesis. 2014 Feb;35(2):469-78. doi: 10.1093/carcin/bgt330. Epub 2013 Oct 1.
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MiR-200 can repress breast cancer metastasis through ZEB1-independent but moesin-dependent pathways.miR-200 可通过非 ZEB1 依赖但肌球蛋白依赖的途径抑制乳腺癌转移。
Oncogene. 2014 Jul 31;33(31):4077-88. doi: 10.1038/onc.2013.370. Epub 2013 Sep 16.
9
Genetic heterogeneity of breast cancer metastasis may be related to miR-21 regulation of TIMP-3 in translation.乳腺癌转移的基因异质性可能与miR-21在翻译过程中对TIMP-3的调控有关。
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MicroRNA-19a-3p inhibits breast cancer progression and metastasis by inducing macrophage polarization through downregulated expression of Fra-1 proto-oncogene.MicroRNA-19a-3p 通过下调 Fra-1 原癌基因的表达诱导巨噬细胞极化,抑制乳腺癌的进展和转移。
Oncogene. 2014 Jun 5;33(23):3014-23. doi: 10.1038/onc.2013.258. Epub 2013 Jul 8.

乳腺癌中的微小RNA:具有临床潜力的致癌基因和肿瘤抑制因子

MicroRNAs in breast cancer: oncogene and tumor suppressors with clinical potential.

作者信息

Wang Wei, Luo Yun-ping

机构信息

Department of Immunology, Institute of Basic Medical Science, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100005, China.

出版信息

J Zhejiang Univ Sci B. 2015 Jan;16(1):18-31. doi: 10.1631/jzus.B1400184.

DOI:10.1631/jzus.B1400184
PMID:25559952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4288941/
Abstract

MicroRNAs (miRs) are small single-stranded RNA molecules, which function as key negative regulators of post-transcriptional modulation in almost all biological processes. Abnormal expression of microRNAs has been observed in various types of cancer including breast cancer. Great efforts have been made to identify an association between microRNA expression profiles and breast cancer, and to understand the functional role and molecular mechanism of aberrant-expressed microRNAs. As research progressed, 'oncogenic microRNAs' and 'tumor suppressive microRNAs' became a focus of interest. The potential of candidate microRNAs from both intercellular (tissue) and extracellular (serum) sources for clinical diagnosis and prognosis was revealed, and treatments involving microRNA achieved some amazing curative effects in cancer disease models. In this review, advances from the most recent studies of microRNAs in one of the most common cancers, breast cancer, are highlighted, especially the functions of specifically selected microRNAs. We also assess the potential value of these microRNAs as diagnostic and prognostic markers, and discuss the possible development of microRNA-based therapies.

摘要

微小RNA(miRs)是小的单链RNA分子,在几乎所有生物过程中作为转录后调控的关键负调节因子发挥作用。在包括乳腺癌在内的各种癌症中均观察到微小RNA的异常表达。人们已付出巨大努力来确定微小RNA表达谱与乳腺癌之间的关联,并了解异常表达的微小RNA的功能作用和分子机制。随着研究的进展,“致癌微小RNA”和“肿瘤抑制微小RNA”成为了关注焦点。来自细胞间(组织)和细胞外(血清)来源的候选微小RNA在临床诊断和预后方面的潜力得以揭示,并且涉及微小RNA的治疗在癌症疾病模型中取得了一些惊人的疗效。在本综述中,重点介绍了对最常见癌症之一乳腺癌中微小RNA的最新研究进展,特别是特定选择的微小RNA的功能。我们还评估了这些微小RNA作为诊断和预后标志物的潜在价值,并讨论了基于微小RNA的疗法的可能发展。