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Survivin expression in human lung cancer and the influence of its downregulation on the biological behavior of human lung cancer cells

机译:Survivin在人肺癌中的表达及其下调对人肺癌细胞生物学行为的影响

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摘要

The aim of the present study was to detect the expression of survivin in human lung cancer and to investigate the influence of its downregulation on the biological behavior of A549 lung cancer cells. The high expression of survivin in human lung cancer was verified by immunohistochemistry. Survivin small interfering RNA (siRNA) and unrelated sequence were synthesized and the siRNA lentiviral vector was constructed. The vector was transfected into A549 lung cancer cells, in which the clone with stable expression was screened out. We blocked the expression of survivin mRNA and protein by RNA interference (RNAi) technique. The downregulation of survivin mRNA and protein expression was confirmed by real-time quantitative PCR and western blotting. The proliferative activity and growth rate of A549 cells were determined by colony formation assay and mononuclear cell direct cytotoxicity assay (MTT assay). The reconstituted basement membrane (RBM) penetrating capacity was determined by cell invasion assay. The cell movement and migratory capacity were detected by wound-healing repair assay. The results showed that the sequence-specific siRNA significantly downregulated the expression of survivin at both the mRNA and protein levels. Downregulation of survivin expression dramatically decreased the invasive and metastatic capacities of the cells, suppressed the proliferation, decelerated the rate of growth, reduced the number of clones on soft agar and decreased the capacity of RBM penetration and migration. In conclusion, survivin, which plays an important role in carcinogenesis and development of lung cancer, can be effectively downregulated using the RNAi technique.
机译:本研究的目的是检测survivin在人肺癌中的表达,并研究其下调对A549肺癌细胞生物学行为的影响。免疫组织化学证实了survivin在人肺癌中的高表达。合成了Survivin小干扰RNA(siRNA)和无关序列,构建了siRNA慢病毒载体。将该载体转染到A549肺癌细胞中,筛选出表达稳定的克隆。我们通过RNA干扰(RNAi)技术阻止了survivin mRNA和蛋白的表达。实时定量PCR和western印迹证实了survivin mRNA和蛋白表达的下调。通过集落形成测定和单核细胞直接细胞毒性测定(MTT测定)确定A549细胞的增殖活性和生长速率。通过细胞侵袭测定来确定重构的基底膜(RBM)的穿透能力。通过伤口愈合修复法检测细胞的运动和迁移能力。结果表明,序列特异性siRNA在mRNA和蛋白质水平均显着下调了survivin的表达。 Survivin表达的下调显着降低了细胞的侵袭和转移能力,抑制了增殖,降低了生长速率,减少了软琼脂上克隆的数量,并降低了RBM渗透和迁移的能力。总之,在RNAi的发生和发展中起重要作用的survivin可以有效地下调。

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