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RNA结合基序蛋白47抑制Nrf2活性以抑制肺腺癌的肿瘤生长。

RNA-binding motif protein 47 inhibits Nrf2 activity to suppress tumor growth in lung adenocarcinoma.

作者信息

Sakurai T, Isogaya K, Sakai S, Morikawa M, Morishita Y, Ehata S, Miyazono K, Koinuma D

机构信息

Department of Molecular Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Ludwig Institute for Cancer Research, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.

出版信息

Oncogene. 2016 Sep 22;35(38):5000-9. doi: 10.1038/onc.2016.35. Epub 2016 Feb 29.

DOI:10.1038/onc.2016.35
PMID:26923328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5036161/
Abstract

RNA-binding proteins provide a new layer of posttranscriptional regulation of RNA during cancer progression. We identified RNA-binding motif protein 47 (RBM47) as a target gene of transforming growth factor (TGF)-β in mammary gland epithelial cells (NMuMG cells) that have undergone the epithelial-to-mesenchymal transition. TGF-β repressed RBM47 expression in NMuMG cells and lung cancer cell lines. Expression of RBM47 correlated with good prognosis in patients with lung, breast and gastric cancer. RBM47 suppressed the expression of cell metabolism-related genes, which were the direct targets of nuclear factor erythroid 2-related factor 2 (Nrf2; also known as NFE2L2). RBM47 bound to KEAP1 and Cullin 3 mRNAs, and knockdown of RBM47 inhibited their protein expression, which led to enhanced binding of Nrf2 to target genomic regions. Knockdown of RBM47 also enhanced the expression of some Nrf2 activators, p21/CDKN1A and MafK induced by TGF-β. Both mitochondrial respiration rates and the side population cells in lung cancer cells increased in the absence of RBM47. Our findings, together with the enhanced tumor formation and metastasis of xenografted mice by knockdown of the RBM47 expression, suggested tumor-suppressive roles for RBM47 through the inhibition of Nrf2 activity.

摘要

RNA结合蛋白在癌症进展过程中为RNA转录后调控增添了新层面。我们将RNA结合基序蛋白47(RBM47)鉴定为已发生上皮-间质转化的乳腺上皮细胞(NMuMG细胞)中转化生长因子(TGF)-β的靶基因。TGF-β抑制NMuMG细胞和肺癌细胞系中RBM47的表达。RBM47的表达与肺癌、乳腺癌和胃癌患者的良好预后相关。RBM47抑制细胞代谢相关基因的表达,这些基因是核因子红细胞2相关因子2(Nrf2;也称为NFE2L2)的直接靶标。RBM47与KEAP1和Cullin 3 mRNA结合,敲低RBM47会抑制它们的蛋白表达,从而导致Nrf2与靶基因组区域的结合增强。敲低RBM47还增强了TGF-β诱导的一些Nrf2激活剂p21/CDKN1A和MafK的表达。在缺乏RBM47的情况下,肺癌细胞中的线粒体呼吸速率和侧群细胞均增加。我们的研究结果,连同敲低RBM47表达后异种移植小鼠肿瘤形成和转移增强,提示RBM47通过抑制Nrf2活性发挥肿瘤抑制作用。

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本文引用的文献

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Comprehensive molecular profiling of lung adenocarcinoma.肺腺癌的全面分子分析。
Nature. 2014 Jul 31;511(7511):543-50. doi: 10.1038/nature13385. Epub 2014 Jul 9.
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A Smad3 and TTF-1/NKX2-1 complex regulates Smad4-independent gene expression.一种Smad3与TTF-1/NKX2-1复合物调控不依赖Smad4的基因表达。
拷贝数扩增诱导长链非编码 RNA LOC101927668 过表达通过募集 hnRNPD 破坏 RBM47/p53/p21 信号促进结直肠癌进展。
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Deubiquitinating enzyme OTUD4 stabilizes RBM47 to induce ATF3 transcription: a novel mechanism underlying the restrained malignant properties of ccRCC cells.去泛素化酶 OTUD4 通过稳定 RBM47 诱导 ATF3 转录:一种新型机制可抑制 ccRCC 细胞的恶性特性。
Apoptosis. 2024 Aug;29(7-8):1051-1069. doi: 10.1007/s10495-024-01953-6. Epub 2024 Mar 30.
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A RBM47 and IGF2BP1 mediated circular FNDC3B-FNDC3B mRNA imbalance is involved in the malignant processes of osteosarcoma.RBM47和IGF2BP1介导的环状FNDC3B-FNDC3B mRNA失衡参与骨肉瘤的恶性进展。
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Dynamic RBM47 ISGylation confers broad immunoprotection against lung injury and tumorigenesis via TSC22D3 downregulation.动态RBM47 ISGylation通过下调TSC22D3赋予对肺损伤和肿瘤发生的广泛免疫保护。
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