Sakurai T, Isogaya K, Sakai S, Morikawa M, Morishita Y, Ehata S, Miyazono K, Koinuma D
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.
Oncogene. 2016 Sep 22;35(38):5000-9. doi: 10.1038/onc.2016.35. Epub 2016 Feb 29.
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.
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。