Abberent expression of oncogenic and tumor-suppressive microRNAs and their target genes in human adenocarcinoma alveolar basal epithelial cells

作者:Tafsiri Elham; Darbouy Mojtaba; Shadmehr Mohammad Behgam; Cho William C; Karimipoor Morteza*
来源:Journal of Cancer Research and Therapeutics, 2016, 12(1): 395-400.
DOI:10.4103/0973-1482.148673

摘要

Context: Lung cancer is one of the most serious types of cancer that often diagnosed at advanced stage. MicroRNAs (miRNAs) are small non-coding molecules which silence gene expression of target gene (s) at posttranscriptional level. They are key regulators of cell cycle, apoptosis, anti-cancer drug responsiveness and metastasis. Aims: Identification of the differential expression level of miR-15a/16, miR-21, miR-34a, miR-126, miR-128 and miR-210 in A549 cell line versus normal tissues and their correlation with selected corresponding target genes. Materials and Methods: A549 cell line was cultured in F-12K medium and miRNA was extracted from normal tissues (2-3 cm adjacent to tumor tissue) and A549 cell line. cDNA was synthesized with specific stem-loop primers for each miRNA, while OligodT primer was used for target genes cDNA synthesis. Real-time quantitative polymerase chain reaction (RT-qPCR) was used to analyze the expression pattern of miRNAs and target genes in A549 and normal non-small cell lung carcinoma (NSCLC) tissues. Results: miR-15a/16, miR-34a, miR-126 and miR-128 were down-regulated significantly (>2-fold change), while miR-21 and miR-210 were up-regulated in A549. Bcl-2 as miR-34a target gene was down-regulated while Hif-1 alpha and Akt-3 were up-regulated that might be miR-210 and miR-34a target genes, respectively. Conclusion: The significant differential expression level of these miRNAs made them as candidate biomarkers in NSCLC tumor tissues of patients. Perhaps Bcl-2 down-regulation and Akt-3 up-regulation can be linked with survival signals in A549 cell line. We can conclude that Bcl-2 and Akt-3 might be therapeutic targets to inhibit cell proliferation in NSCLC.

  • 出版日期2016-3