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LAPSER1:一个来自10q24.3的新型候选肿瘤抑制基因。

LAPSER1: a novel candidate tumor suppressor gene from 10q24.3.

作者信息

Cabeza-Arvelaiz Y, Thompson T C, Sepulveda J L, Chinault A C

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Oncogene. 2001 Oct 11;20(46):6707-17. doi: 10.1038/sj.onc.1204866.

Abstract

Numerous LOH and mutation analysis studies in different tumor tissues, including prostate, indicate that there are multiple tumor suppressor genes (TSGs) present within the human chromosome 8p21-22 and 10q23-24 regions. Recently, we showed that LZTS1 (or FEZ1), a putative TSG located on 8p22, has the potential to function as a cell growth modulator. We report here the cloning, gene organization, cDNA sequence characterization and expression analysis of LAPSER1, an LZTS1-related gene. This gene maps within a subregion of human chromosome 10q24.3 that has been reported to be deleted in various cancers, including prostate tumors, as frequently as the neighboring PTEN locus. The complete LAPSER1 cDNA sequence encodes a predicted protein containing various domains resembling those typically found in transcription factors (P-Box, Q-rich and multiple leucine zippers). LAPSER1 is expressed at the highest levels in normal prostate and testis, where multiple isoforms are seen, some of which are either undetectable or differentially expressed in some prostate tumor tissues and cell lines. Over-expression of LAPSER1 cDNA strongly inhibited cell growth and colony-forming efficiencies of most cancer cells assessed. Together these data suggest that LAPSER1 is another gene involved in the regulation of cell growth whose loss of function may contribute to the development of cancer.

摘要

在包括前列腺在内的不同肿瘤组织中进行的大量杂合性缺失(LOH)和突变分析研究表明,人类染色体8p21 - 22和10q23 - 24区域存在多个肿瘤抑制基因(TSG)。最近,我们发现位于8p22的假定肿瘤抑制基因LZTS1(或FEZ1)具有作为细胞生长调节剂发挥作用的潜力。我们在此报告LZTS1相关基因LAPSER1的克隆、基因结构、cDNA序列特征及表达分析。该基因定位于人类染色体10q24.3的一个亚区域,据报道在包括前列腺肿瘤在内的多种癌症中,该区域与邻近的PTEN基因座一样频繁缺失。完整的LAPSER1 cDNA序列编码一种预测蛋白,该蛋白包含多种类似于转录因子中常见的结构域(P盒、富含Q的结构域和多个亮氨酸拉链)。LAPSER1在正常前列腺和睾丸中表达水平最高,在这些组织中可见多种异构体,其中一些在某些前列腺肿瘤组织和细胞系中无法检测到或表达存在差异。LAPSER1 cDNA的过表达强烈抑制了所评估的大多数癌细胞的细胞生长和集落形成效率。这些数据共同表明,LAPSER1是另一个参与细胞生长调控的基因,其功能丧失可能促成癌症的发生。

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