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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Liu, Yuanhua Yang, Zhen Wang, Junxia Liu, Guanghui Li, Dongyan Zhang, Xiefu |
| Description | Author Affiliation: Liu G ( Department of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.); Liu Y ( Department of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.); Yang Z ( Department of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.); Wang J ( Department of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.); Li D ( Department of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.); Zhang X ( Department of Gastrointestinal Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.) |
| Abstract | Recent advances in the understanding of microRNA have rendered microRNAs (miRNAs) a compelling novel class of biomarker in cancer biology. However, the specific function of miRNA18a (miR18a) in colorectal cancer (CRC) remains unclear. In the present study, the role of miR18a in the carcinogenesis of CRC was investigated. miR18a expression was assessed in CRC specimens and cell lines using reverse transcriptionquantitative polymerase chain reaction (RTqPCR). The targets of miR18a were predicted using bioinformatics tools. Luciferase reporter assays were used to confirm the functional association between miR18a and its target genes. The effect of miR18a on cell proliferation, invasion and migration was confirmed in vitro by a methylthiazol tetrazolium assay, cell invasion assay, and wound healing assay. Gene and protein expression was examined using RTqPCR and western blotting, respectively. It was demonstrated that the expression of miR18a in CRC tissues and cell lines was markedly lower than in normal control tissues and cells, respectively. In addition, miR18a inhibited cell proliferation, invasion and migration in CRC cells. Moreover, TATA boxbinding proteinlike protein 1 (TBPL1) was identified as a potential target gene of miR18a in the bioinformatics analysis and luciferase reporter assays, and miR18a directly inhibited TBPL1 expression by targeting its 3'untranslated region. Furthermore, TBPL1 was downregulated and inversely correlated with miR18a expression in tissues. These findings demonstrate that miR18a exhibits a protective role in CRC via inhibiting proliferation, invasion and migration of CRC cells by directly targeting the TBPL1 gene. |
| ISSN | 17912997 |
| e-ISSN | 17913004 |
| Journal | Molecular Medicine Reports |
| Issue Number | 5 |
| Volume Number | 12 |
| Language | English |
| Publisher | Spandidos Publications |
| Publisher Date | 2015-11-01 |
| Publisher Place | Greece |
| Access Restriction | Open |
| Subject Keyword | Colon Pathology Colorectal Neoplasms Genetics Gene Expression Regulation, Neoplastic Micrornas Tata Box Binding Protein-like Proteins Carcinogenesis Cell Line, Tumor Cell Proliferation Metabolism Genes, Tumor Suppressor Neoplasm Invasiveness Discipline Molecular Biology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics Biochemistry Molecular Biology Cancer Research Molecular Medicine Oncology |
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