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NANOGP8表达通过反式激活胃癌MKN-45细胞中的DBC1来调节胃癌细胞进展。

NANOGP8 expression regulates gastric cancer cell progression by transactivating DBC1 in gastric cancer MKN-45 cells.

作者信息

Li Li, Feng Ru, Fei Sujuan, Cao Jiang, Zhu Qinqin, Ji Guozhong, Zhou Jianwei

机构信息

Department of Molecular Cell Biology and Toxicology, Jiangsu Key Laboratory of Cancer Biomarkers, Prevention and Treatment, Cancer Center, Nanjing Medical University, Nanjing, Jiangsu 211166, P.R. China.

Department of Gastroenterology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu 221000, P.R. China.

出版信息

Oncol Lett. 2019 Jan;17(1):555-563. doi: 10.3892/ol.2018.9595. Epub 2018 Oct 18.

Abstract

NANOGP8 is one of the NANOG pseudogenes and is expressed together with NANOG in multiple tumor tissues and cell lines. The biological functions of NANOGP8 in progression of gastric cancer are unclear. In the present study, the role of NANOGP8 was investigated in gastric cancer cells. The gathered data demonstrated that NANOG expression in both mRNA and protein was elevated in gastric cancer cell lines relative to a normal gastric epithelial cell line. Downregulation of NANOGP8 inhibited cell proliferation and increased apoptosis in human gastric carcinoma cell lines. Furthermore, silencing of NANOGP8 suppressed tumor growth . Interestingly, it was identified that deleted in breast cancer 1 (DBC1) expression was also markedly downregulated following NANOGP8 knockdown. DNA microarray and dual-luciferase assays further indicated that NANOGP8 may bind to the DBC1 promoter region and regulate DBC1 expression. Therefore, the gathered data provided evidence that NANOGP8 contributes to progression of gastric cancer via DBC1 and may have potential translational significance.

摘要

NANOGP8是NANOG假基因之一,在多种肿瘤组织和细胞系中与NANOG共同表达。NANOGP8在胃癌进展中的生物学功能尚不清楚。在本研究中,我们研究了NANOGP8在胃癌细胞中的作用。收集的数据表明,相对于正常胃上皮细胞系,胃癌细胞系中NANOG的mRNA和蛋白表达均升高。NANOGP8的下调抑制了人胃癌细胞系的细胞增殖并增加了细胞凋亡。此外,NANOGP8的沉默抑制了肿瘤生长。有趣的是,我们发现乳腺癌1(DBC1)缺失表达在NANOGP8敲低后也明显下调。DNA微阵列和双荧光素酶测定进一步表明,NANOGP8可能与DBC1启动子区域结合并调节DBC1表达。因此,收集的数据提供了证据,表明NANOGP8通过DBC1促进胃癌进展,可能具有潜在的转化意义。

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