Long non-coding RNA HOTAIR, a c-Myc activated driver of malignancy, negatively regulates miRNA-130a in gallbladder cancer

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• 作者：Ming-zhe Ma (1) (2)
  Chun-xiao Li (3)
  Yan Zhang (4)
  Ming-zhe Weng (1)
  Ming-di Zhang (1)
  Yi-yu Qin (1)
  Wei Gong (1)
  Zhi-wei Quan (1)
  
  1. Department of General Surgery ; Xinhua Hospital ; Shanghai Jiaotong University School of Medicine ; 1665 Kongjiang Road ; Shanghai ; 200092 ; People鈥檚 Republic of China
  2. Department of General Surgery ; Taixing people鈥檚 Hospital ; Yangzhou University School of Medicine ; Kragujevac ; Jiangsu Province ; China
  3. Department of Dermatology ; Xinhua Hospital ; Shanghai Jiaotong University School of Medicine ; Shanghai ; China
  4. Department of Gastroenterology ; Yijishan Hospital affiliated to Wannan medical College ; Wuhu ; Anhui ; China
  
• 关键词：Long non ; coding RNA ; HOTAIR ; miRNA ; 130a ; c ; Myc ; Gallbladder cancer
• 刊名：Molecular Cancer
• 出版年：2014
• 出版时间：December 2014
• 年：2014
• 卷：13
• 期：1
• 全文大小：1,311 KB
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• 刊物主题：Cancer Research; Oncology;
• 出版者：BioMed Central
• ISSN：1476-4598

文摘

Background Protein coding genes account for only about 2% of the human genome, whereas the vast majority of transcripts are non-coding RNAs including long non-coding RNAs. A growing volume of literature has proposed that lncRNAs are important players in cancer. HOTAIR was previously shown to be an oncogene and negative prognostic factor in a variety of cancers. However, the factors that contribute to its upregulation and the interaction between HOTAIR and miRNAs are largely unknown. Methods A computational screen of HOTAIR promoter was conducted to search for transcription-factor-binding sites. HOTAIR promoter activities were examined by luciferase reporter assay. The function of the c-Myc binding site in the HOTAIR promoter region was tested by a promoter assay with nucleotide substitutions in the putative E-box. The association of c-Myc with the HOTAIR promoter in vivo was confirmed by chromatin immunoprecipitation assay and Electrophoretic mobility shift assay. A search for miRNAs with complementary base paring with HOTAIR was performed utilizing online software program. Gain and loss of function approaches were employed to investigate the expression changes of HOTAIR or miRNA-130a. The expression levels of HOTAIR, c-Myc and miRNA-130a were examined in 65 matched pairs of gallbladder cancer tissues. The effects of HOTAIR and miRNA-130a on gallbladder cancer cell invasion and proliferation was tested using in vitro cell invasion and flow cytometric assays. Results We demonstrate that HOTAIR is a direct target of c-Myc through interaction with putative c-Myc target response element (RE) in the upstream region of HOTAIR in gallbladder cancer cells. A positive correlation between c-Myc and HOTAIR mRNA levels was observed in gallbladder cancer tissues. We predicted that HOTAIR harbors a miRNA-130a binding site. Our data showed that this binding site is vital for the regulation of miRNA-130a by HOTAIR. Moreover, a negative correlation between HOTAIR and miRNA-130a was observed in gallbladder cancer tissues. Finally, we demonstrate that the oncogenic activity of HOTAIR is in part through its negative regulation of miRNA-130a. Conclusion Together, these results suggest that HOTAIR is a c-Myc-activated driver of malignancy, which acts in part through repression of miRNA-130a.