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本文引用的文献

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Overexpression of miR-122 promotes the hepatic differentiation and maturation of mouse ESCs through a miR-122/FoxA1/HNF4a-positive feedback loop.miR-122的过表达通过miR-122/FoxA1/HNF4a正反馈环促进小鼠胚胎干细胞的肝向分化和成熟。
Liver Int. 2014 Feb;34(2):281-95. doi: 10.1111/liv.12239. Epub 2013 Jul 9.
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Epigenetic modulation of the miR-200 family is associated with transition to a breast cancer stem-cell-like state.miR-200 家族的表观遗传调控与向乳腺癌干细胞样状态的转变有关。
J Cell Sci. 2013 May 15;126(Pt 10):2256-66. doi: 10.1242/jcs.122275. Epub 2013 Mar 22.
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Critical regulation of miR-200/ZEB2 pathway in Oct4/Sox2-induced mesenchymal-to-epithelial transition and induced pluripotent stem cell generation.在 Oct4/Sox2 诱导的间充质到上皮转化和诱导多能干细胞生成中,miR-200/ZEB2 通路的关键调控。
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A unilateral negative feedback loop between miR-200 microRNAs and Sox2/E2F3 controls neural progenitor cell-cycle exit and differentiation.miR-200 微 RNA 与 Sox2/E2F3 之间的单向负反馈环控制神经祖细胞的细胞周期退出和分化。
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MicroRNA profiling of a CD133(+) spheroid-forming subpopulation of the OVCAR3 human ovarian cancer cell line.CD133(+) 球体形成亚群的 OVCAR3 人卵巢癌细胞系的 microRNA 谱分析。
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The origin of cancer stem cells.癌症干细胞的起源。
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MiR-181 mediates cell differentiation by interrupting the Lin28 and let-7 feedback circuit.miR-181 通过中断 Lin28 和 let-7 反馈回路来介导细胞分化。
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MicroRNA regulation of cancer stem cells.微小 RNA 对肿瘤干细胞的调控。
Cancer Res. 2011 Sep 15;71(18):5950-4. doi: 10.1158/0008-5472.CAN-11-1035. Epub 2011 Sep 13.
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The microRNA miR-34a inhibits prostate cancer stem cells and metastasis by directly repressing CD44.微小 RNA miR-34a 通过直接抑制 CD44 抑制前列腺癌干细胞和转移。
Nat Med. 2011 Feb;17(2):211-5. doi: 10.1038/nm.2284. Epub 2011 Jan 16.
10
MicroRNA Regulation of Embryonic Stem Cell Self-Renewal and Differentiation.微小 RNA 对胚胎干细胞自我更新和分化的调控。
Adv Exp Med Biol. 2010;695:105-17. doi: 10.1007/978-1-4419-7037-4_8.

微小 RNA 参与癌症干细胞的自我更新和分化。

MicroRNAs are involved in the self-renewal and differentiation of cancer stem cells.

机构信息

Mitchell Cancer Institute, University of South Alabama, Alabama Mobile, USA.

出版信息

Acta Pharmacol Sin. 2013 Nov;34(11):1374-80. doi: 10.1038/aps.2013.134. Epub 2013 Oct 14.

DOI:10.1038/aps.2013.134
PMID:24122008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3849030/
Abstract

MicroRNAs (miRNAs) are small non-coding RNA molecules, whose primary function is to regulate gene expression at the post-transcriptional/translational levels. MiRNAs play crucial roles in normal biological processes and are commonly dys-regulated in human diseases. Stem cells are regarded as the "mother" cells of all types of differentiated cells that comprise tissues and organs of the body. A novel hypothesis proposes that tumors are composed of heterogeneous cells derived from cancer stem cells, which have self-renewal and differentiation capabilities similar to those of normal stem cells. Cancer stem cells have been isolated and characterized from various tumors. Given recent studies supporting the critical regulatory roles of miRNAs in the self-renewal and differentiation of cancer stem cells, better understanding the functions of miRNAs will provide invaluable insights into the prevention of tumorigenesis and tumor progression. In this review, we will summarize the research progress in the study of miRNAs involved in the self-renewal and differentiation of cancer stem cells.

摘要

微小 RNA(miRNAs)是一类小的非编码 RNA 分子,其主要功能是在转录后/翻译水平上调节基因表达。miRNAs 在正常的生物学过程中发挥着关键作用,并且在人类疾病中通常失调。干细胞被认为是身体组织和器官中所有类型分化细胞的“母”细胞。一个新的假说提出,肿瘤由源自癌症干细胞的异质细胞组成,这些细胞具有类似于正常干细胞的自我更新和分化能力。已经从各种肿瘤中分离和鉴定出癌症干细胞。鉴于最近的研究支持 miRNAs 在癌症干细胞的自我更新和分化中的关键调节作用,更好地理解 miRNAs 的功能将为预防肿瘤发生和肿瘤进展提供宝贵的见解。在这篇综述中,我们将总结 miRNA 在癌症干细胞自我更新和分化中的作用的研究进展。