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鉴定编码一种类Krüppel锌指蛋白的ZASC1作为食管鳞状细胞癌3q26扩增的新靶点。

Identification of ZASC1 encoding a Krüppel-like zinc finger protein as a novel target for 3q26 amplification in esophageal squamous cell carcinomas.

作者信息

Imoto Issei, Yuki Yasuhiro, Sonoda Itaru, Ito Tetsuo, Shimada Yutaka, Imamura Masayuki, Inazawa Johji

机构信息

Department of Molecular Cytogenetics, Medical Research Institute, Tokyo Medical and Dental University, Japan.

出版信息

Cancer Res. 2003 Sep 15;63(18):5691-6.

Abstract

Among the transcription factors that direct proliferation, differentiation, and death of cells, several Krüppel-like zinc finger molecules such as GLI1 and ZNF147 can become oncogenic when the genes encoding them are overexpressed by the DNA amplification mechanism. Here, we report the discovery of a novel member of this class, ZASC1, from a recently reported critical region of 3q26 amplification frequently observed in various squamous cell carcinomas, including esophageal squamous cell carcinomas (ESCs). The deduced 485-amino acid protein product of ZASC1 contained a putative nuclear localization signal; the exogenously transfected ZASC1 was translocated into cell nuclei. ZASC1 was frequently coamplified and subsequently overexpressed with PIK3CA in our panel of ESC cell lines and primary tumors. In patients with ESC, a higher mRNA expression level of ZASC1 appeared to be associated with shorter overall survival, and a multivariate analysis demonstrated that ZASC1 mRNA expression was an independent prognosticator. In addition, exogenous expression of ZASC1 promoted the growth of ESC cells, whereas down-regulation of ZASC1 expression by means of an antisense oligonucleotide suppressed the growth of ESC cells. Taken together, our results suggest that ZASC1 might be involved in the pathogenesis of ESC as one of the targets for 3q26 amplification, alone or in concert with other targets.

摘要

在指导细胞增殖、分化和死亡的转录因子中,一些Krüppel样锌指分子,如GLI1和ZNF147,当编码它们的基因通过DNA扩增机制过度表达时,可能会致癌。在此,我们报告了这类分子的一个新成员ZASC1的发现,它来自最近报道的在包括食管鳞状细胞癌(ESCs)在内的各种鳞状细胞癌中频繁观察到的3q26扩增关键区域。ZASC1推导的485个氨基酸的蛋白质产物含有一个假定的核定位信号;外源性转染的ZASC1被转运到细胞核中。在我们的一组ESC细胞系和原发性肿瘤中,ZASC1经常与PIK3CA共同扩增并随后过度表达。在ESC患者中,ZASC1较高的mRNA表达水平似乎与较短的总生存期相关,多变量分析表明ZASC1 mRNA表达是一个独立的预后指标。此外,ZASC1的外源性表达促进了ESC细胞的生长,而通过反义寡核苷酸下调ZASC1表达则抑制了ESC细胞的生长。综上所述,我们的结果表明,ZASC1可能作为3q26扩增的靶点之一,单独或与其他靶点一起参与ESC的发病机制。

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