Cdx1通过降低细胞周期蛋白D1基因的表达来抑制人结肠癌细胞的增殖。

Cdx1 inhibits the proliferation of human colon cancer cells by reducing cyclin D1 gene expression.

作者信息

Lynch John, Keller Matthew, Guo Rong-Jun, Yang Donald, Traber Peter

机构信息

Division of Gastroenterology, Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Oncogene. 2003 Sep 25;22(41):6395-407. doi: 10.1038/sj.onc.1206770.

Abstract

The transcription factor Cdx1 regulates intestine-specific gene expression and enterocyte differentiation. It has been hypothesized to play a role in regulating intestinal cell proliferation; however, the mechanism for this effect remains elusive. In a prior study, we demonstrated that Cdx1 expression reduced the proliferation of a nontransformed intestinal cell line. This study tests the hypothesis that Cdx1 expression inhibits colon cancer cell proliferation by reducing cyclin D1 gene expression. Cdx1 expression markedly reduced cancer cell proliferation and DNA synthesis and induced an accumulation of cells in G0/G1. A transcriptionally inactive Cdx1 mutant could not elicit this effect, suggesting that it required Cdx1 transcriptional activity. Cdx1 expression increased the hypophosphorylation of the retinoblastoma (pRb) and p130 proteins. Reductions in G1 cyclin-dependant kinase (cdk) activity accompanied this effect. Cyclin D1 mRNA and protein levels were diminished by Cdx1 expression. Restoration of cyclin D1 expression reversed the G0/G1 block and induced pRb hyperphosphorylation. Lastly, Cdx1 expression did not alter cyclin D1 mRNA stability but did reduce cyclin D1 promoter activity, suggesting that Cdx1 acts to diminish cyclin D1 gene transcription. We conclude that Cdx1 reduces the proliferation of human colon cancer cells by reducing cyclin D1 gene transcription.

摘要

转录因子Cdx1调节肠道特异性基因表达和肠上皮细胞分化。据推测,它在调节肠道细胞增殖中发挥作用;然而,这种作用的机制仍不清楚。在先前的一项研究中,我们证明Cdx1的表达降低了一种未转化的肠道细胞系的增殖。本研究检验了Cdx1的表达通过降低细胞周期蛋白D1基因表达来抑制结肠癌细胞增殖的假说。Cdx1的表达显著降低了癌细胞的增殖和DNA合成,并诱导细胞在G0/G1期积累。转录无活性的Cdx1突变体不能引发这种效应,表明这需要Cdx1的转录活性。Cdx1的表达增加了视网膜母细胞瘤(pRb)和p130蛋白的低磷酸化。这种效应伴随着G1期细胞周期蛋白依赖性激酶(cdk)活性的降低。Cdx1的表达使细胞周期蛋白D1的mRNA和蛋白水平降低。细胞周期蛋白D1表达的恢复逆转了G0/G1期阻滞并诱导了pRb的高磷酸化。最后,Cdx1的表达没有改变细胞周期蛋白D1 mRNA的稳定性,但确实降低了细胞周期蛋白D1启动子的活性,表明Cdx1的作用是减少细胞周期蛋白D1基因的转录。我们得出结论,Cdx1通过减少细胞周期蛋白D1基因转录来降低人结肠癌细胞的增殖。

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