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Axin 通过β-catenin 下调 TCF-4 的转录,而不是 p53,并抑制肺癌细胞的增殖和侵袭。

Axin downregulates TCF-4 transcription via beta-catenin, but not p53, and inhibits the proliferation and invasion of lung cancer cells.

机构信息

Department of Pathology, The First Affiliated Hospital and College of Basic Medical Sciences of China Medical University, Shenyang 110001, China.

出版信息

Mol Cancer. 2010 Feb 2;9:25. doi: 10.1186/1476-4598-9-25.

Abstract

BACKGROUND

We previously reported that overexpression of Axin downregulates T cell factor-4 (TCF-4) transcription. However, the mechanism(s) by which Axin downregulates the transcription and expression of TCF-4 is not clear. It has been reported that beta-catenin promotes and p53 inhibits TCF-4 transcription, respectively. The aim of this study was to investigate whether beta-catenin and/or p53 is required for Axin-mediated downregulation of TCF-4.

RESULTS

Axin mutants that lack p53/HIPK2 and/or beta-catenin binding domains were expressed in lung cancer cells, BE1 (mutant p53) and A549 (wild type p53). Expression of Axin or AxinDeltap53 downregulates beta-catenin and TCF-4, and knock-down of beta-catenin upregulates TCF-4 in BE1 cells. However, expression of AxinDeltabeta-ca into BE1 cells did not downregulate TCF-4 expression. These results indicate that Axin downregulates TCF-4 transcription via beta-catenin. Although overexpression of wild-type p53 also downregulates TCF-4 in BE1 cells, cotransfection of p53 and AxinDeltabeta-ca did not downregulate TCF-4 further. These results suggest that Axin does not promote p53-mediated downregulation of TCF-4. Axin, AxinDeltap53, and AxinDeltabeta-ca all downregulated beta-catenin and TCF-4 in A549 cells. Knock-down of p53 upregulated beta-catenin and TCF-4, but cotransfection of AxinDeltabeta-ca and p53 siRNA resulted in downregulation of beta-catenin and TCF-4. These results indicate that p53 is not required for Axin-mediated downregulation of TCF-4. Knock-down or inhibition of GSK-3beta prevented Axin-mediated downregulation of TCF-4. Furthermore, expression of Axin and AxinDeltap53, prevented the proliferative and invasive ability of BE1 and A549, expression of AxinDeltabeta-ca could only prevented the proliferative and invasive ability effectively.

CONCLUSIONS

Axin downregulates TCF-4 transcription via beta-catenin and independently of p53. Axin may also inhibits the proliferation and invasion of lung cancer cells via beta-catenin and p53.

摘要

背景

我们之前报道过,Axin 的过表达会下调 T 细胞因子-4(TCF-4)的转录。然而,Axin 下调 TCF-4 转录和表达的机制尚不清楚。已有报道称,β-catenin 分别促进和 p53 抑制 TCF-4 的转录。本研究旨在探讨 β-catenin 和/或 p53 是否是 Axin 介导的 TCF-4 下调所必需的。

结果

在肺癌细胞 BE1(突变型 p53)和 A549(野生型 p53)中表达缺乏 p53/HIPK2 和/或 β-catenin 结合域的 Axin 突变体。Axin 或 AxinDeltap53 的表达会下调 β-catenin 和 TCF-4,而在 BE1 细胞中敲低 β-catenin 会上调 TCF-4。然而,在 BE1 细胞中表达 AxinDeltabeta-ca 并不能下调 TCF-4 的表达。这些结果表明,Axin 通过 β-catenin 下调 TCF-4 的转录。尽管野生型 p53 的过表达也会下调 BE1 细胞中的 TCF-4,但共转染 p53 和 AxinDeltabeta-ca 并不能进一步下调 TCF-4。这些结果表明,Axin 不会促进 p53 介导的 TCF-4 下调。Axin、AxinDeltap53 和 AxinDeltabeta-ca 均在 A549 细胞中下调 β-catenin 和 TCF-4。敲低 p53 会上调 β-catenin 和 TCF-4,但共转染 AxinDeltabeta-ca 和 p53 siRNA 会导致 β-catenin 和 TCF-4 的下调。这些结果表明,p53 不是 Axin 介导的 TCF-4 下调所必需的。敲低或抑制 GSK-3β 可阻止 Axin 介导的 TCF-4 下调。此外,Axin 和 AxinDeltap53 的表达可防止 BE1 和 A549 的增殖和侵袭能力,而 AxinDeltabeta-ca 的表达仅能有效防止增殖和侵袭能力。

结论

Axin 通过 β-catenin 并独立于 p53 下调 TCF-4 转录。Axin 还可能通过 β-catenin 和 p53 抑制肺癌细胞的增殖和侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc9d/2827467/6ae1bc0b7e09/1476-4598-9-25-1.jpg

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