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抑癌基因 UCHL1 与 p53/MDM2/ARF 形成复合物,促进 p53 信号通路的激活,在鼻咽癌中常被沉默。

The tumor suppressor UCHL1 forms a complex with p53/MDM2/ARF to promote p53 signaling and is frequently silenced in nasopharyngeal carcinoma.

机构信息

State Key Laboratory in Oncology in South China/Cancer Epigenetics Laboratory, Department of Clinical Oncology, Sir YK Pao Center for Cancer, Hong Kong Cancer Institute, Hong Kong.

出版信息

Clin Cancer Res. 2010 Jun 1;16(11):2949-58. doi: 10.1158/1078-0432.CCR-09-3178. Epub 2010 Apr 15.

Abstract

PURPOSE

Nasopharyngeal carcinoma is prevalent in southern China and Southeast Asia, with distinct geographic and ethnic distribution. One candidate susceptibility locus has been identified at 4p11-14, with the associated candidate gene(s) not identified yet. This study investigated the role of ubiquitin carboxyl-terminal hydrolase L1 (UCHL1) in nasopharyngeal carcinoma pathogenesis.

EXPERIMENTAL DESIGN

UCHL1 expression and methylation were examined in nasopharyngeal carcinoma. Furthermore, the mechanism of its tumor-suppressive function was elucidated in nasopharyngeal carcinoma cells.

RESULTS

Through genomewide expression profiling, we identified UCHL1, a 4p14 gene normally expressed in normal upper respiratory tract tissues, being silenced in all nasopharyngeal carcinoma cell lines. Its silencing is mediated by CpG methylation because UCHL1 promoter methylation was detected in all silenced cell lines, and pharmacologic demethylation reactivated UCHL1 expression along with concomitant promoter demethylation. UCHL1 methylation was also frequently detected in primary tumors but only weakly detected in few normal nasopharyngeal tissues, indicating that the methylation-mediated silencing of UCHL1 is important in nasopharyngeal carcinoma pathogenesis. Ectopic UCHL1 expression dramatically inhibited the growth of nasopharyngeal carcinoma cells through promoting tumor cell apoptosis. We further found that UCHL1 formed a complex with p53/p14(ARF)/Mdm2 p53 binding protein homolog (mouse), MDM2 and activated the p53 signaling pathway. UCHL1 expression extended p53 and p14(ARF) protein half-life and shortened MDM2 protein half-life.

CONCLUSIONS

These results indicate that UCHL1 could deubiquitinate p53 and p14(ARF) and ubiquitinate MDM2 for p53 stabilization to promote p53 signaling, thus involved in nasopharyngeal carcinoma pathogenesis, whereas it is frequently silenced in this tumor.

摘要

目的

鼻咽癌在中国南方和东南亚地区较为常见,具有明显的地理和种族分布特征。一个候选易感基因座已在 4p11-14 被确定,但其相关候选基因尚未被鉴定。本研究旨在探讨泛素羧基末端水解酶 L1(UCHL1)在鼻咽癌发病机制中的作用。

实验设计

检测鼻咽癌中 UCHL1 的表达和甲基化情况。进一步阐明其在鼻咽癌细胞中的抑瘤作用机制。

结果

通过全基因组表达谱分析,我们发现 UCHL1 是一个正常在上呼吸道组织中表达的 4p14 基因,在所有鼻咽癌细胞系中均被沉默。其沉默是由 CpG 甲基化介导的,因为在所有被沉默的细胞系中均检测到 UCHL1 启动子甲基化,而药物去甲基化可重新激活 UCHL1 的表达,同时伴有启动子去甲基化。UCHL1 甲基化在原发肿瘤中也经常被检测到,但在少数正常鼻咽组织中仅被弱检测到,表明 UCHL1 甲基化介导的沉默在鼻咽癌发病机制中很重要。外源性 UCHL1 表达可通过促进肿瘤细胞凋亡显著抑制鼻咽癌细胞的生长。我们进一步发现 UCHL1 与 p53/p14(ARF)/Mdm2 p53 结合蛋白同源物(鼠)、MDM2 形成复合物,并激活 p53 信号通路。UCHL1 表达延长了 p53 和 p14(ARF)蛋白的半衰期,缩短了 MDM2 蛋白的半衰期。

结论

这些结果表明,UCHL1 可通过去泛素化 p53 和 p14(ARF)并泛素化 MDM2 稳定 p53,从而促进 p53 信号通路,参与鼻咽癌的发病机制,而在这种肿瘤中常被沉默。

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