首页> 外文会议>2010 4th International Conference on Bioinformatics and Biomedical Engineering >Cellular Biological Influences of Down-Regulated MicroRNA-143 on Human Bronchial Epithelial Cells
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Cellular Biological Influences of Down-Regulated MicroRNA-143 on Human Bronchial Epithelial Cells

机译:下调的microRNA 143对人支气管上皮细胞的细胞生物学影响。

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MicroRNAs (miRNAs) were recently identified to play crucial roles in tumorigenesis processes. In present study, we explored the potential influence of miRNA-143 on several cellular biological processes related with lung cancer development in human bronchial epithelial cells 16-HBE. Chemosynthesis anti-miR-143 was used to down-regulate expression of miR-143. Cell proliferation was detected by methyl thiazolyl tetrazolium (MTT) assay after 24, 48 and 72 h transfection of anti-miR-143. Apoptosis and cell cycle were detected by flow cytometry after 48 h transfection of anti-miR-143. The results revealed that there were no significant differences in cell activity and apoptosis between transfection group and control group (P>0.05). Compared with control group, DNA content of G1 period of anti-miRNA-143 group had a mild decrease (P<0.05), DNA content of S period of anti-miRNA-143 group had a mild increase (P<0.05). The results suggested that down-regulated miR-143 induce S arrest of cell cycle. MiR-143 may associate with lung cancer development through influence cell cycle progression. The cooperation between more miRNAs and environmental carcinogen on the tumorigenesis of lung cancer needs to further investigate.
机译:最近识别MicroRNAs(miRNA)以在肿瘤内酯过程中发挥关键作用。在目前的研究中,我们探讨了MiRNA-143对人支气管上皮细胞16-HBE中肺癌发育有关的几种细胞生物学过程的潜在影响。化学合成抗miR-143用于下调miR-143的表达。在24,48和72小时的抗miR-143转染后,通过甲基噻唑基四唑(MTT)测定检测细胞增殖。通过流式细胞术在48小时转染抗miR-143后,通过流式细胞术检测细胞凋亡和细胞周期。结果表明,转染组和对照组之间的细胞活性和细胞凋亡没有显着差异(p> 0.05)。与对照组相比,抗miRNA-143组G1时期的DNA含量轻微降低(P <0.05),S抗miRNA-143组的DNA含量轻微增加(P <0.05)。结果表明,下调的miR-143诱导逮捕细胞周期。 MiR-143可以通过影响细胞周期进展与肺癌发育相关联。对肺癌肿瘤瘤的更多miRNA和环境致癌物质的合作需要进一步调查。

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