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本文引用的文献

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MicroRNA Involvement in Osteosarcoma.微小RNA与骨肉瘤的关系
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2
miR-409-3p inhibits HT1080 cell proliferation, vascularization and metastasis by targeting angiogenin.miR-409-3p 通过靶向血管生成素抑制 HT1080 细胞增殖、血管生成和转移。
Cancer Lett. 2012 Oct 28;323(2):171-9. doi: 10.1016/j.canlet.2012.04.010. Epub 2012 Apr 21.
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MicroRNA-21 correlates with tumorigenesis in malignant peripheral nerve sheath tumor (MPNST) via programmed cell death protein 4 (PDCD4).MicroRNA-21 通过程序性细胞死亡蛋白 4(PDCD4)与恶性外周神经鞘瘤(MPNST)的发生相关。
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Down-regulation of miR-183 promotes migration and invasion of osteosarcoma by targeting Ezrin.下调 miR-183 通过靶向 Ezrin 促进骨肉瘤的迁移和侵袭。
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MicroRNA-34a inhibits the proliferation and metastasis of osteosarcoma cells both in vitro and in vivo.MicroRNA-34a 抑制骨肉瘤细胞的体外和体内增殖和转移。
PLoS One. 2012;7(3):e33778. doi: 10.1371/journal.pone.0033778. Epub 2012 Mar 21.
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An integrated analysis of miRNA and gene copy numbers in xenografts of Ewing's sarcoma.异种移植中尤文肉瘤 miRNA 和基因拷贝数的综合分析。
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miRNA signatures associate with pathogenesis and progression of osteosarcoma.miRNA 特征与骨肉瘤的发病机制和进展相关。
Cancer Res. 2012 Apr 1;72(7):1865-77. doi: 10.1158/0008-5472.CAN-11-2663. Epub 2012 Feb 20.
8
MiR-155 is a liposarcoma oncogene that targets casein kinase-1α and enhances β-catenin signaling.miR-155 是一种脂肪肉瘤致癌基因,其靶标是酪蛋白激酶-1α,并增强 β-连环蛋白信号。
Cancer Res. 2012 Apr 1;72(7):1751-62. doi: 10.1158/0008-5472.CAN-11-3027. Epub 2012 Feb 20.
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Downregulation of microRNAs miR-1, -206 and -29 stabilizes PAX3 and CCND2 expression in rhabdomyosarcoma.miR-1、miR-206 和 miR-29 的下调稳定了横纹肌肉瘤中 PAX3 和 CCND2 的表达。
Lab Invest. 2012 Apr;92(4):571-83. doi: 10.1038/labinvest.2012.10. Epub 2012 Feb 13.
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Frequent alterations and epigenetic silencing of differentiation pathway genes in structurally rearranged liposarcomas.结构重排脂肪肉瘤中分化途径基因的频繁改变和表观遗传沉默。
Cancer Discov. 2011 Dec;1(7):587-97. doi: 10.1158/2159-8290.CD-11-0181.

微小 RNA 介导的人类肉瘤中的基因调控。

MicroRNA-mediated gene regulations in human sarcomas.

机构信息

Department of Surgery, University of Minnesota, 11-212 Moos Tower (Mail Code: MMC 195), 515 Delaware St, S.E, Minneapolis, MN 55455, USA.

出版信息

Cell Mol Life Sci. 2012 Nov;69(21):3571-85. doi: 10.1007/s00018-012-1127-x. Epub 2012 Aug 25.

DOI:10.1007/s00018-012-1127-x
PMID:22922987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11114979/
Abstract

Sarcomas are a heterogeneous group of tumors with mesenchymal origins. Sarcomas are broadly classified into bone and soft tissue sarcomas with over 50 subtypes. Despite recent advances in sarcoma classification and treatment strategies, the prognosis of some aggressive sarcoma types remains poor due to treatment infectiveness and development of drug resistance. A better understanding of sarcoma pathobiology will significantly increase the potential for the development of therapeutics and treatment strategies. Recently, expressions of microRNAs (miRNA), a class of small non-coding RNAs, have been found to be deregulated in many sarcomas and are implicated in sarcoma pathobiology. Comprehensive understanding of gene regulatory networks mediated by miRNAs in each sarcoma type and the conservation of some shared/conserved miRNA-gene networks could be potentially investigated in the prevention, diagnosis, prognosis and as multi-modal treatment options in these cancers. In this review, we will discuss the current knowledge of miRNA-gene regulatory networks in various sarcoma types and give a perspective of the complex multilayer miRNA-mediated gene regulation in sarcomas.

摘要

肉瘤是一组具有间充质来源的异质性肿瘤。肉瘤广泛分为骨和软组织肉瘤,有 50 多种亚型。尽管肉瘤分类和治疗策略最近取得了进展,但由于治疗的感染性和耐药性的发展,一些侵袭性肉瘤类型的预后仍然较差。更好地了解肉瘤的病理生物学将显著增加治疗和治疗策略的发展潜力。最近,小 RNA(miRNA)的表达,一类小的非编码 RNA,已被发现失调在许多肉瘤,并参与肉瘤病理生物学。全面了解 miRNA 在每种肉瘤类型中介导的基因调控网络,以及一些共享/保守的 miRNA-基因网络的保守性,可能会在这些癌症的预防、诊断、预后和多模式治疗选择中得到研究。在这篇综述中,我们将讨论各种肉瘤类型中 miRNA-基因调控网络的现有知识,并对肉瘤中复杂的多层 miRNA 介导的基因调控进行展望。