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性别决定区Y框蛋白2促进肺鳞状细胞癌生长并直接靶向细胞周期蛋白D1。

Sex-Determining Region Y-box 2 Promotes Growth of Lung Squamous Cell Carcinoma and Directly Targets Cyclin D1.

作者信息

Li Chiguan, He Bingwen, Huang Cuiping, Yang Huaping, Cao Liming, Huang Jun, Hu Chengping

机构信息

1 Department of Respiration, Chenzhou First People's Hospital , Chenzhou, China .

2 Department of Respiration, Xiangya Hospital, Central South University , Changsha, China .

出版信息

DNA Cell Biol. 2017 Apr;36(4):264-272. doi: 10.1089/dna.2016.3562. Epub 2017 Feb 2.

Abstract

Sex-determining region Y-box 2 (SOX2) is an oncogene known to be amplified and overexpressed in various human malignancies, including lung squamous cell carcinoma (SCC). However, the role played by SOX2 in lung SCC development remains to be elucidated. We measured the levels of SOX2 and cyclin D1 mRNA and protein expression in lung SCC tissues and a lung SCC cell line, and found that both levels were dramatically upregulated in specimens of lung SCC tissue when compared with their expression levels in samples of adjacent nonneoplastic tissue. The lung SCC cell line also showed higher levels of SOX2 and cyclin D1 expression than a normal human bronchial epithelium cell line. After using RNA interference to knock down SOX2 expression in NCI-H520 lung SCC cells, their proliferation was reduced. Furthermore, overexpression of SOX2 promoted the proliferation of normal human bronchial epithelium cells. To further determine whether cyclin D1 was downstream target gene of SOX2, we measured the levels of cyclin D1 expression that occurred when SOX2 was knocked down or overexpressed. SOX2 knockdown significantly decreased the levels of cyclin D1 mRNA and protein expression, while SOX2 overexpression upregulated the levels of cyclin D1. We used bioinformatics data to identify potential cyclin D1 promoter binding sites for SOX2. Results of luciferase reporter assays, electrophoretic mobility shift assays, and chromatin immunoprecipitation assays confirmed that cyclin D1 was a direct target of transcription factor SOX2 in human lung SCC cells.

摘要

性别决定区Y框蛋白2(SOX2)是一种癌基因,已知在包括肺鳞状细胞癌(SCC)在内的多种人类恶性肿瘤中发生扩增和过表达。然而,SOX2在肺SCC发生发展中所起的作用仍有待阐明。我们检测了肺SCC组织和一种肺SCC细胞系中SOX2和细胞周期蛋白D1的mRNA及蛋白表达水平,发现与相邻非肿瘤组织样本中的表达水平相比,肺SCC组织样本中这两种水平均显著上调。该肺SCC细胞系中SOX2和细胞周期蛋白D1的表达水平也高于正常人支气管上皮细胞系。在使用RNA干扰敲低NCI-H520肺SCC细胞中的SOX2表达后,其增殖受到抑制。此外,SOX2的过表达促进了正常人支气管上皮细胞的增殖。为进一步确定细胞周期蛋白D1是否为SOX2的下游靶基因,我们检测了SOX2被敲低或过表达时细胞周期蛋白D1的表达水平。敲低SOX2显著降低了细胞周期蛋白D1的mRNA和蛋白表达水平,而SOX2的过表达则上调了细胞周期蛋白D1的水平。我们利用生物信息学数据鉴定了SOX2潜在的细胞周期蛋白D1启动子结合位点。荧光素酶报告基因检测、电泳迁移率变动分析和染色质免疫沉淀分析结果证实,在人肺SCC细胞中细胞周期蛋白D1是转录因子SOX2的直接靶标。

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