南方医科大学学报 ›› 2013, Vol. 33 ›› Issue (08): 1122-.

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TGF-β1诱导的肿瘤细胞CSRNP1/AXUD1 基因的表达及转录调节机制

邓凡,李松玉,许万福,邹志鹏,柯志勇,曾方银   

  • 出版日期:2013-08-20 发布日期:2013-08-20

AXIN1-related CSRNP1 mRNA expression and its transcriptional regulation in TGF-β1- induced tumor cells

  • Online:2013-08-20 Published:2013-08-20

摘要: 目的探讨TGF-β1诱导的肿瘤细胞中CSRNP1/AXUD1基因的表达及其调控机制。方法分别用不同浓度的TGF-β1或
相同浓度下不同处理时间处理指数生长期的人肺腺癌细胞A549和人前列腺癌细胞PC-3,荧光定量RT-PCR检测TGF-β1对两
种肿瘤细胞中半胱氨酸-丝氨酸蛋白(cystein-serine-rich nuclear protein, CSRNP1)基因表达的剂量和时间依赖性效应;培养的
A549细胞血清饥饿后,分别在有无TGF-β1(20 ng/ml)和环己亚胺(30 μg/ml)作用下处理24 h,检测TGF-β1诱导的CSRNP1基
因的表达是否需要新蛋白的合成;最后,分别将SMAD3表达质粒flag-SMAD3和显性失活突变体表达质粒(flag-SMAD3-mu
转染A549细胞中,并以空质粒pcDNA3.1作为对照。血清饥饿后,进行有无TGF-β1(20 ng/ml)处理24 h,Western blot 确定外
源性SMAD3的过表达,荧光定量RT-PCR检测SMAD3的过表达对TGF-β1诱导的CSRNP1基因表达的影响。结果TGF-β1以
浓度和时间依赖的方式诱导肿瘤细胞中CSRNP1 基因的表达,并需要新的蛋白合成。SMAD3 的过表达增加TGF-β1 诱导的
CSRNP1的表达,而显性失活的SMAD3突变体(SMAD3-mu)的过表达则显著降低TGF-β1诱导的CSRNP1的表达。结论肿瘤
细胞中TGF-β1可能通过激活SMAD3 及其下游信号通路而诱导CSRNP1基因的表达。

Abstract: Objective To investigate AXIN1-related CSRNP1 gene expression and the mechanism of its transcriptional
regulation in TGF-β1-induced tumor cells. Methods Human lung carcinoma A549 cells or human prostate cancer PC3 cells
were 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 time
effect of TGF-β1 on CSRNP1 mRNA expression in the tumor cells were evaluated with real-time RT-PCR. A549 cells were also
treated with TGF-β1 and cycloheximide to clarify whether CSRNP1 expression induced by TGF-β1 required de novo protein
synthesis. A549 cells transfected with pcDNA3.1, flag-SMAD3, or flag-SMAD3-mu, after serum starvation, were treated with
or without TGF-β1 (20 ng/mL) for 24 h, and the overexpression of wild-type SMAD3 and dominant negative SMAD3-mu
mutant were confirmed by Western blotting. The effect of SMAD3 or SMAD3-mu overexpression on CSRNP1 mRNA
expression was also measured by real-time RT-PCR. Results In both A549 and PC3 cells, TGF-β1 dose- and time-dependently
stimulated CSRNP1 expression, which required de novo protein synthesis in A549 cells. Overexpression of wild-type SMAD3
significantly increased the expression of CSRNP1 mRNA induced by TGF-β1, while overexpression of dominant negative
SMAD3 mutant remarkably reduced CSRNP1 mRNA expression in response to TGF-β1 in A549 cells. Conclusion TGF-β1 may
contribute to CSRNP1 expression through SMAD3 activation and downstream signaling in tumor cells.