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本文引用的文献

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The miRNA-kallikrein axis of interaction: a new dimension in the pathogenesis of prostate cancer.微小 RNA-激肽原轴相互作用:前列腺癌发病机制的新维度。
Biol Chem. 2012 Apr;393(5):379-89. doi: 10.1515/hsz-2011-0246.
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The dark side of E2F1: in transit beyond apoptosis.E2F1 的阴暗面:在凋亡之外的运输过程中。
Cancer Res. 2012 Feb 1;72(3):571-5. doi: 10.1158/0008-5472.CAN-11-2575.
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eIF5A isoforms and cancer: two brothers for two functions?eIF5A 异构体与癌症:两种异构体,两种功能?
Amino Acids. 2013 Jan;44(1):103-9. doi: 10.1007/s00726-011-1182-x. Epub 2011 Dec 3.
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L-Mimosine blocks cell proliferation via upregulation of B-cell translocation gene 2 and N-myc downstream regulated gene 1 in prostate carcinoma cells.L-刺毛黧豆素通过上调 B 细胞易位基因 2 和 N- myc 下游调节基因 1 抑制前列腺癌细胞增殖。
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The RNA-binding protein HuR opposes the repression of ERBB-2 gene expression by microRNA miR-331-3p in prostate cancer cells.RNA 结合蛋白 HuR 拮抗 microRNA miR-331-3p 对前列腺癌细胞中 ERBB-2 基因表达的抑制作用。
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MicroRNAs and the cell cycle.微小RNA与细胞周期
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Characterization of the small RNA transcriptomes of androgen dependent and independent prostate cancer cell line by deep sequencing.通过深度测序对雄激素依赖性和非依赖性前列腺癌细胞系的小 RNA 转录组进行表征。
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MicroRNA regulation of growth factor receptor signaling in human cancer cells.人类癌细胞中微小RNA对生长因子受体信号传导的调控
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调控前列腺癌细胞中 deoxyhypusine hydroxylase(DOHH)的表达,该酶可催化 eIF5A 的激活,受 miR-331-3p 和 miR-642-5p 的调控。

Regulation of expression of deoxyhypusine hydroxylase (DOHH), the enzyme that catalyzes the activation of eIF5A, by miR-331-3p and miR-642-5p in prostate cancer cells.

机构信息

Laboratory for Cancer Medicine, Western Australian Institute for Medical Research and University of Western Australia Centre for Medical Research, Royal Perth Hospital, Perth, Western Australia 6000, Australia.

Uropath Pty, Ltd., West Leederville, Western Australia 6007, Australia; School of Pathology and Laboratory Medicine, University of Western Australia, Nedlands, Western Australia 6009, Australia.

出版信息

J Biol Chem. 2012 Oct 12;287(42):35251-35259. doi: 10.1074/jbc.M112.374686. Epub 2012 Aug 20.

DOI:10.1074/jbc.M112.374686
PMID:22908221
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3471734/
Abstract

The enzyme deoxyhypusine hydroxylase (DOHH) catalyzes the activation of eukaryotic translation initiation factor (eIF5A), a protein essential for cell growth. Using bioinformatic predictions and reporter gene assays, we have identified a 182-nt element within the DOHH 3'-untranslated region (3'-UTR) that contains a number of target sites for miR-331-3p and miR-642-5p. Quantitative RT-PCR studies demonstrated overexpression of DOHH mRNA and underexpression of miR-331-3p and miR-642-5p in several prostate cancer cell lines compared with normal prostate epithelial cells. Transient overexpression of miR-331-3p and/or miR-642-5p in DU145 prostate cancer cells reduced DOHH mRNA and protein expression and inhibited cell proliferation. We observed synergistic growth inhibition with the combination of miR-331-3p and miR-642-5p and mimosine, a pharmacological DOHH inhibitor. Finally, we identified a significant inverse relationship between the expression of miR-331-3p or miR-642-5p and DOHH in a cohort of human prostate cancer tissues. Our results suggest a novel role for miR-331-3p and miR-642-5p in the control of prostate cancer cell growth via the regulation of DOHH expression and eIF5A activity.

摘要

脱羟酶(DOHH)能够催化真核翻译起始因子(eIF5A)的激活,而该蛋白对细胞生长至关重要。通过生物信息学预测和报告基因检测,我们在 DOHH 3'非翻译区(3'-UTR)内鉴定出一段含有 miR-331-3p 和 miR-642-5p 多个靶位点的 182nt 元件。定量 RT-PCR 研究表明,与正常前列腺上皮细胞相比,几种前列腺癌细胞系中 DOHH mRNA 的表达上调,而 miR-331-3p 和 miR-642-5p 的表达下调。瞬时过表达 miR-331-3p 和/或 miR-642-5p 可降低 DU145 前列腺癌细胞中的 DOHH mRNA 和蛋白表达,并抑制细胞增殖。我们观察到 miR-331-3p 和 miR-642-5p 与脯氨酸类似物(一种药理学 DOHH 抑制剂)联合使用具有协同生长抑制作用。最后,我们在一组人类前列腺癌组织中发现 miR-331-3p 或 miR-642-5p 的表达与 DOHH 的表达呈显著负相关。我们的研究结果表明,miR-331-3p 和 miR-642-5p 通过调控 DOHH 的表达和 eIF5A 的活性,在控制前列腺癌细胞生长方面发挥着新的作用。