RPS12-specific shRNA inhibits the proliferation, migration of BGC823 gastric cancer cells with S100A4 as a downstream effector

作者: DANQI CHEN , RUIXIU ZHANG , WEI SHEN , HAO FU , SHANSHAN LIU

DOI: 10.3892/IJO.2013.1872

关键词:

摘要: Our previous study using suppression subtractive hybridization (SSH), cDNA microarray and semi-quantitative RT-PCR showed that RPS12 was overexpressed in gastric cancer it closely related to metastasis. However, the role of is not clear, which led us conduct current further investigate effects on proliferation migration cells, also explore underlying molecular mechanisms. RNA interference used inhibit expression RPS12. The S100A4 cells determined western blot analysis. Cell were detected by MTT transwell assay, respectively. In addition, promoter activity measured a Dual-Luciferase Reporter Assay System. We found RNAi‑mediated downregulation reduced BGC823 SGC7901 cells. Further results inhibition decreased demonstrated ectopic reversed ability after findings provide first demonstration plays important roles regulating can mediate as downstream effector.

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