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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.

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。

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