项目名称: Versican 3'-非翻译区(3'-UTR)作为非编码竞争内源性RNA(ceRNA)通过调控MicroRNAs的功能在乳腺癌中的作用
项目编号: No.81472454
项目类型: 面上项目
立项/批准年度: 2015
项目学科: 医药、卫生
项目作者: 方玲
作者单位: 吉林大学
项目金额: 72万元
中文摘要: 研究非编码RNA之间的相互调节机制从而调控生命体已成为又一新兴研究热点。我们的研究表明,非编码3'-UTR能够调节内源性miRNA的功能(Nature Communications; Nucleic Acids Research; FASEB J.);且Versican在细胞凋亡中起着重要作用(Cancer Research)。基于此本课题将继续研究乳腺癌中Versican 3'-UTR作为非编码竞争内源性RNA(ceRNA)调控miRNA 及其相关靶蛋白的作用及作用机制;研究Versican 3'-UTR对乳腺癌细胞的调控作用,并用siRNAs确认其功能;研究其转基因小鼠和乳腺癌标本中Versican亚型的表达,从而研究其对乳腺癌的作用。初步结果显示Versican 3'-UTR结合miR-199a-3p,并抑制了乳腺癌细胞增殖。本课题将为乳腺癌的发生机制和诊治提供重要理论依据及新策略。
中文关键词: C21_乳腺肿瘤;Versican;3'-非翻译区;MicroRNA;竞争内源性RNA;非编码RNA
英文摘要: The Roles of Versican 3'-Untranslated Region (3'-UTR) Functioning as The Non-coding Competing Endogenous RNA (ceRNA) by Regulating MicroRNAs Activity in Breast Carcinoma Nowadays in life sciences, it is becoming another focus area that study on the interaction mechanism in non-coding RNA functions in regulating cell activities. In our previous studies, we found that the non-coding 3'untranslated region (UTR) plays an important role in the regulation of endogenous miRNA functions (Rutnam ZJ, Nature Communications 5:2914, 1-15, 2014; Jeyapalan et al., Nucleic Acids Research 39(8):3026-41, 2010; Fang L and Du WW et al., FASEB J. 27(3), 907-19, 2013). On the other hand, we reported that Versican can play important roles in cell apoptosis (LaPierre et al., Cancer Research, 67, 4742-4750, 2007). Based on the above results, we will investigate the roles and mechanism of Versican 3'-untranslated region (3'-UTR) in regulating cell activities by functioning as the non-coding competitive endogenous RNA (ceRNA), which can bind and regulate endogenous miRNA functions, thus modulating its potential targets. In addition, we will use breast carcinoma cell lines stably transfected with Versican 3'-UTR to examine its effects on tumor cell proliferation, survival, apoptosis, migration, invasion, colony formation, and endothelial cell activities. We will also design Versican 3'-UTR siRNAs to confirm the functions of Versican 3'-UTR. Furthermore, we will use transgenic mice expressing Versican 3'-UTR and clinical breast carcinoma patients samples to study whether or not expression of this 3'-UTR promotes breast carcinoma growth by regulating expression of Versican isoforms. Finally, in our preliminary results we found that 4T1 cells transfected with Versican 3'-UTR showed reduction of miR-199a-3p compared with cells transfected with the control vector. And in the 4T1 cell line expression of Versican 3'-UTR reduced breast carcinoma cells proliferation. Therefore, we believe that this project will provide important new views and strategies on the pathogenesis, diagnosis and treatment of breast carcinoma.
英文关键词: Breast carcinoma;Versican 3'-UTR;MicroRNA;ceRNA;Non-coding RNA