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本文引用的文献

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MicroRNA 29c is down-regulated in nasopharyngeal carcinomas, up-regulating mRNAs encoding extracellular matrix proteins.微小RNA 29c在鼻咽癌中表达下调,可上调编码细胞外基质蛋白的信使核糖核酸。
Proc Natl Acad Sci U S A. 2008 Apr 15;105(15):5874-8. doi: 10.1073/pnas.0801130105. Epub 2008 Apr 4.
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microRNAs: small molecules with big roles - C. elegans to human cancer.微小RNA:作用重大的小分子——从秀丽隐杆线虫到人类癌症
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microRNAs in viral oncogenesis.病毒致癌作用中的微小RNA
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Tumor protein 53-induced nuclear protein 1 expression is repressed by miR-155, and its restoration inhibits pancreatic tumor development.肿瘤蛋白53诱导的核蛋白1的表达受miR-155抑制,其恢复可抑制胰腺肿瘤发展。
Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16170-5. doi: 10.1073/pnas.0703942104. Epub 2007 Oct 2.
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A microRNA component of the p53 tumour suppressor network.p53肿瘤抑制网络的一个微小RNA组分。
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Retroviral activation of the mir-106a microRNA cistron in T lymphoma.T淋巴瘤中mir-106a微小RNA顺反子的逆转录病毒激活
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Human T-cell leukaemia virus type 1 (HTLV-1) infectivity and cellular transformation.人类嗜T淋巴细胞病毒1型(HTLV-1)的感染性与细胞转化
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Abnormal microRNA-16 locus with synteny to human 13q14 linked to CLL in NZB mice.与人类13q14存在同线性的异常微小RNA - 16基因座与新西兰黑小鼠的慢性淋巴细胞白血病相关。
Blood. 2007 Jun 15;109(12):5079-86. doi: 10.1182/blood-2007-02-071225. Epub 2007 Mar 9.
9
Colitis and colitis-associated cancer are exacerbated in mice deficient for tumor protein 53-induced nuclear protein 1.在缺乏肿瘤蛋白53诱导核蛋白1的小鼠中,结肠炎和结肠炎相关癌症会加剧。
Mol Cell Biol. 2007 Mar;27(6):2215-28. doi: 10.1128/MCB.01454-06. Epub 2007 Jan 22.
10
Decreased expression of tumor protein p53-induced nuclear protein 1 (TP53INP1) in breast carcinoma.乳腺癌中肿瘤蛋白p53诱导核蛋白1(TP53INP1)表达降低。
Anticancer Res. 2006 Nov-Dec;26(6B):4391-5.

微小RNA(miR-93和miR-130b)以及肿瘤蛋白53诱导核蛋白1肿瘤抑制因子在人T细胞嗜淋巴细胞病毒1引起的细胞生长失调中的作用。

Roles for microRNAs, miR-93 and miR-130b, and tumor protein 53-induced nuclear protein 1 tumor suppressor in cell growth dysregulation by human T-cell lymphotrophic virus 1.

作者信息

Yeung Man Lung, Yasunaga Jun-ichirou, Bennasser Yamina, Dusetti Nelson, Harris David, Ahmad Nafees, Matsuoka Masao, Jeang Kuan-Teh

机构信息

Molecular Virology Section, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, Maryland, USA.

出版信息

Cancer Res. 2008 Nov 1;68(21):8976-85. doi: 10.1158/0008-5472.CAN-08-0769.

DOI:10.1158/0008-5472.CAN-08-0769
PMID:18974142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2596768/
Abstract

A role for microRNAs (miRNA) in human T-cell leukemia virus 1 (HTLV-1)-mediated cellular transformation has not been described. Here, we profiled miRNA expression in HTLV-1-transformed human T-cell lines and primary peripheral blood mononuclear cells from adult T-cell leukemia patients. Analyses of 11 different profiles revealed six miRNAs that were consistently up-regulated. Two of the up-regulated miRNAs (miR-93 and miR-130b) target the 3' untranslated region (3'UTR) of the mRNA for a tumor suppressor protein, tumor protein 53-induced nuclear protein 1 (TP53INP1). A low expression level of TP53INP1 protein was found in HTLV-1-transformed cells. Additionally, when antagomirs were used to knock down miR-93 and miR-130b in these cells, the expression of TP53INP1 was increased, suggesting that the latter is regulated inside cells by the former. A role for TP53INP1 in regulating cell growth was established by experiments that showed that enhanced TP53INP1 expression increased apoptosis. Collectively, the findings implicate a miR-93/miR-130b-TP53INP1 axis that affects the proliferation and survival of HTLV-1-infected/transformed cells.

摘要

微小RNA(miRNA)在人类T细胞白血病病毒1型(HTLV-1)介导的细胞转化中的作用尚未见报道。在此,我们分析了HTLV-1转化的人类T细胞系以及成体T细胞白血病患者外周血单个核细胞中的miRNA表达。对11种不同图谱的分析揭示了6种持续上调的miRNA。其中两种上调的miRNA(miR-93和miR-130b)靶向一种肿瘤抑制蛋白——肿瘤蛋白53诱导核蛋白1(TP53INP1)的mRNA的3'非翻译区(3'UTR)。在HTLV-1转化的细胞中发现TP53INP1蛋白的表达水平较低。此外,当使用抗miR来敲低这些细胞中的miR-93和miR-130b时,TP53INP1的表达增加,这表明前者在细胞内对后者具有调控作用。通过实验证实增强TP53INP1表达会增加细胞凋亡,从而确立了TP53INP1在调节细胞生长中的作用。总体而言,这些发现表明存在一个影响HTLV-1感染/转化细胞增殖和存活的miR-93/miR-130b-TP53INP1轴。