Journal of Southern Medical University ›› 2013, Vol. 33 ›› Issue (08): 1122-.
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Abstract: Objective To investigate AXIN1-related CSRNP1 gene expression and the mechanism of its transcriptionalregulation in TGF-β1-induced tumor cells. Methods Human lung carcinoma A549 cells or human prostate cancer PC3 cellswere treated with TGF-β1 at different doses (0, 20, 40, and 80 ng/ml) or at 20 ng/ml for 0, 8, 12, or 24 h, and the dose and timeeffect of TGF-β1 on CSRNP1 mRNA expression in the tumor cells were evaluated with real-time RT-PCR. A549 cells were alsotreated with TGF-β1 and cycloheximide to clarify whether CSRNP1 expression induced by TGF-β1 required de novo proteinsynthesis. A549 cells transfected with pcDNA3.1, flag-SMAD3, or flag-SMAD3-mu, after serum starvation, were treated withor without TGF-β1 (20 ng/mL) for 24 h, and the overexpression of wild-type SMAD3 and dominant negative SMAD3-mumutant were confirmed by Western blotting. The effect of SMAD3 or SMAD3-mu overexpression on CSRNP1 mRNAexpression was also measured by real-time RT-PCR. Results In both A549 and PC3 cells, TGF-β1 dose- and time-dependentlystimulated CSRNP1 expression, which required de novo protein synthesis in A549 cells. Overexpression of wild-type SMAD3significantly increased the expression of CSRNP1 mRNA induced by TGF-β1, while overexpression of dominant negativeSMAD3 mutant remarkably reduced CSRNP1 mRNA expression in response to TGF-β1 in A549 cells. Conclusion TGF-β1 maycontribute to CSRNP1 expression through SMAD3 activation and downstream signaling in tumor cells.
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https://www.j-smu.com/EN/Y2013/V33/I08/1122