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TP63 P2 启动子功能分析鉴定 β-连环蛋白为 ΔNp63 表达的关键调节因子。

TP63 P2 promoter functional analysis identifies β-catenin as a key regulator of ΔNp63 expression.

机构信息

Université de Lyon, Lyon, France.

出版信息

Oncogene. 2011 Nov 17;30(46):4656-65. doi: 10.1038/onc.2011.171. Epub 2011 Jun 6.

Abstract

The ΔNp63 protein, a product of the TP63 gene that lacks the N-terminal domain, has a critical role in the maintenance of self renewal and progenitor capacity in several types of epithelial tissues. ΔNp63 is frequently overexpressed in squamous cell carcinoma (SCC) and in some other epithelial tumours. This overexpression may contribute to tumour progression through dominant-negative effects on the transcriptionally active (TA) isoforms of the p53 family (TAp63, TAp73 and p53), as well as through independent mechanisms. However, the molecular basis of ΔNp63 overexpression is not fully understood. Here, we show that the expression of ΔNp63 is regulated by the Wnt/β-catenin pathway in human hepatocellular carcinoma (HCC) and SCC cell lines. This regulation operates in particular through TCF/LEF sites present in the P2 promoter of TP63. In addition, we show that ΔNp63 and β-catenin are frequently coexpressed and accumulated in oesophageal SCC, but not in HCC. These results suggest that activation of the β-catenin pathway may contribute to overexpression of ΔNp63 during tumour progression, in a cell type-specific manner.

摘要

ΔNp63 蛋白是 TP63 基因的产物,缺少 N 端结构域,在几种上皮组织中维持自我更新和祖细胞能力方面发挥着关键作用。ΔNp63 在鳞状细胞癌(SCC)和其他一些上皮肿瘤中经常过表达。这种过表达可能通过对 p53 家族的转录激活(TA)异构体(TAp63、TAp73 和 p53)的显性负效应以及通过独立的机制促进肿瘤进展。然而,ΔNp63 过表达的分子基础尚不完全清楚。在这里,我们表明 Wnt/β-catenin 通路在人肝癌(HCC)和 SCC 细胞系中调节 ΔNp63 的表达。这种调节特别通过存在于 TP63 的 P2 启动子中的 TCF/LEF 位点起作用。此外,我们表明ΔNp63 和β-catenin 在食管 SCC 中经常共表达和积累,但在 HCC 中则不然。这些结果表明,β-catenin 通路的激活可能导致肿瘤进展过程中 ΔNp63 的过表达,这是一种细胞类型特异性的方式。

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