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迁移和侵袭增强因子1是一种诱导核因子κB的基因,可在体外和体内增强人前列腺癌细胞的增殖和侵袭能力。

Migration and Invasion Enhancer 1 Is an NF-ĸB-Inducing Gene Enhancing the Cell Proliferation and Invasion Ability of Human Prostate Carcinoma Cells In Vitro and In Vivo.

作者信息

Chang Kang-Shuo, Tsui Ke-Hung, Lin Yu-Hsiang, Hou Chen-Pang, Feng Tsui-Hsia, Juang Horng-Heng

机构信息

Department of Anatomy, College of Medicine, Chang Gung University, Kwei-Shan, Tao-Yuan 33302, Taiwan.

Institute of Biomedicine, College of Medicine, Chang Gung University, Kwei-Shan, Tao-Yuan 33302, Taiwan.

出版信息

Cancers (Basel). 2019 Oct 2;11(10):1486. doi: 10.3390/cancers11101486.

Abstract

Migration and invasion enhancer 1 (MIEN1) is a membrane-anchored protein and exists in various cancerous tissues. However, the roles of MIEN1 in prostate cancer have not yet been clearly addressed. We determined the expression, biological functions, and regulatory mechanisms of MIEN1 in the prostate. The results of immunohistochemical analysis indicated that MIEN1 was expressed specifically in epithelial cells and significantly higher in adenocarcinoma as compared to in normal tissues. MIEN1 enhanced in vitro cell proliferation, invasion, and in vivo tumorigenesis. Meanwhile, MIEN1 attenuated cisplatin-induced apoptosis in PC-3 cells. Overexpression of NF-ĸB-inducing kinase (NIK) enhanced MIEN1 expression, while overexpression of NF-ĸB inhibitor α (IĸBα) blocked MIEN1 expression in PC-3 cells. In prostate carcinoma cells, MIEN1 provoked Akt phosphorylation; moreover, MIEN1 downregulated N-myc downstream regulated 1 (NDRG1) but upregulated interleukin-6 (IL-6) gene expression. MK2206, an Akt inhibitor, impeded the modulation of MIEN1 on NDRG1 and IL-6 expressions. Our studies suggest that MIEN1 is an NF-ĸB downstream oncogene in the human prostate. Accordingly, the modulation of Akt signaling in the gene expressions of NDRG1 and IL-6 may account for the functions of MIEN1 in cell proliferation, invasion, and tumorigenesis in prostate carcinoma cells.

摘要

迁移和侵袭增强因子1(MIEN1)是一种膜锚定蛋白,存在于多种癌组织中。然而,MIEN1在前列腺癌中的作用尚未得到明确阐述。我们确定了MIEN1在前列腺中的表达、生物学功能及调控机制。免疫组织化学分析结果表明,MIEN1特异性表达于上皮细胞,与正常组织相比,在腺癌中的表达显著更高。MIEN1增强体外细胞增殖、侵袭及体内肿瘤发生。同时,MIEN1减弱顺铂诱导的PC-3细胞凋亡。NF-κB诱导激酶(NIK)的过表达增强MIEN1表达,而NF-κB抑制剂α(IκBα)的过表达在PC-3细胞中阻断MIEN1表达。在前列腺癌细胞中,MIEN1激发Akt磷酸化;此外,MIEN1下调N-myc下游调控因子1(NDRG1)但上调白细胞介素-6(IL-6)基因表达。Akt抑制剂MK2206阻碍MIEN1对NDRG1和IL-6表达的调控。我们的研究表明,MIEN1是人类前列腺中NF-κB下游的癌基因。因此,Akt信号在NDRG1和IL-6基因表达中的调控作用可能解释了MIEN1在前列腺癌细胞增殖、侵袭和肿瘤发生中的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/6826896/8eefff263fbf/cancers-11-01486-g001.jpg

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