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pmid26617792
      Int+J+Clin+Exp+Pathol 2015 ; 8 (9 ): 10800-7
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  • MiR-142-3p functions as a potential tumor suppressor directly targeting HMGB1 in non-small-cell lung carcinoma #MMPMID26617792
  • Xiao P ; Liu WL
  • Int J Clin Exp Pathol 2015[]; 8 (9 ): 10800-7 PMID26617792 show ga
  • BACKGROUND: microRNAs (miRNAs) play a significant role in cancer development and progression by regulating the expression of oncogenes or tumor suppressor genes. Previous study using microarrays demonstrated that miR-142-3p was downregulated in patients with Non-small-cell lung carcinoma (NSCLC). However, the functional role of miR-142-3p in NSCLC is still unclear. MATERIAL AND METHOD: Real-time quantitative PCR was applied to evaluate the expression level of miRNA-142-3p in NSCLC and normal samples. The cell proliferation of NSCLC cells was analyzed by MTT and colony formation assay after miR-142-3p transfection. Luciferase activities assay, cotransfection and Western blot were used to reveal that the predicted target genes of miR-125b were direct and specific. RESULTS: In this study, we demonstrate miR-142-3p was downregulated in NSCLC tissues and cell lines. We demonstrated that the overexpression of miR-142-3p inhibits NSCLC cell proliferation and induced cell apoptosis. Furthermore, we demonstrate HMGB1 was a directly target of miR-142-3p in NSCLC cells, and confirmed the target specificity between miR-142-3p and the HMGB1 3'-untranslated region by luciferase reporter assay. CONCLUSIONS: These results suggest that miR-142-3p may be a tumor suppressor through the downregulation of HMGB1 in NSCLC. miR-142-3p may be a tumor suppressor and a potential therapeutic agent for patients with NSCLC.
  • |3' Untranslated Regions [MESH]
  • |Aged [MESH]
  • |Apoptosis [MESH]
  • |Binding Sites [MESH]
  • |Carcinoma, Non-Small-Cell Lung/genetics/*metabolism/pathology [MESH]
  • |Cell Line, Tumor [MESH]
  • |Cell Proliferation [MESH]
  • |Computational Biology [MESH]
  • |Databases, Genetic [MESH]
  • |Female [MESH]
  • |Gene Expression Regulation, Neoplastic [MESH]
  • |HMGB1 Protein/genetics/*metabolism [MESH]
  • |Humans [MESH]
  • |Lung Neoplasms/genetics/*metabolism/pathology [MESH]
  • |Male [MESH]
  • |MicroRNAs/genetics/*metabolism [MESH]
  • |Middle Aged [MESH]
  • |Signal Transduction [MESH]
  • |Time Factors [MESH]


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