Effect of NeuroD Gene Silencing on the Migration and Invasion of Human Pancreatic Cancer Cells PANC-1
Copyright policy )Effect of NeuroD Gene Silencing on the Migration and Invasion of Human Pancreatic Cancer Cells PANC-1
The aim of this study is to investigate the influence of Lenti-EGFP-NeuroD-miR, RNAi lentiviral expression vector, on the expression level of NeuroD and migration, and invasion of PANC-1 cell line. PANC-1 cells were cultured and cotransfected with Lenti-EGFP-NeuroD-miR and Lenti-GFP. The infection rate of lentivirus was determined by fluorescence. The interfering effection by the expression of NeuroD mRNA in PANC-1 cells was analyzed by real-time PCR after transfected. Biological behavior of PANC-1 cells transinfected was observed, and the migration and invasion were studied by transwell assay. Intrapancreatic allografts model in nude mice was established to observe the effects of NeuroD on tumorigenesis, tumor growth, and invasion in vivo. The expression of NeuroD mRNA decreased significantly after RNAi lentivirus transinfecting PANC-1 cell. The cell's migration and invasion ability decreased obviously as soon as down regulate of NeuroD in PANC-1 cells. Comparing with control group, the tumors were smaller in size and the invasiveness was inhibited after 8 weeks intrapancreatic allografts in nude mice. Lenti-EGFP-NeuroD-miR transfected into PANC-1 cells shows a stable, effective, and especial blocking expression of NeuroD in mRNA level. The RNAi of lentiviral vector target NeuroD can reduce the migration and invasion abilities of PANC-1 cells.
- Changhai Hospital China (People's Republic of)
- Second Military Medical University China (People's Republic of)
Male, Wound Healing, Carcinogenesis, Genetic Vectors, Lentivirus, Nerve Tissue Proteins, Pancreatic Neoplasms, Mice, Cell Transformation, Neoplastic, Cell Movement, Cell Line, Tumor, Gene Knockdown Techniques, Basic Helix-Loop-Helix Transcription Factors, Animals, Humans, Female, Neoplasm Invasiveness, RNA Interference
Male, Wound Healing, Carcinogenesis, Genetic Vectors, Lentivirus, Nerve Tissue Proteins, Pancreatic Neoplasms, Mice, Cell Transformation, Neoplastic, Cell Movement, Cell Line, Tumor, Gene Knockdown Techniques, Basic Helix-Loop-Helix Transcription Factors, Animals, Humans, Female, Neoplasm Invasiveness, RNA Interference
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