Suppr超能文献

Nm23-H1的下游靶点:利用DNA微阵列技术对CAL 27细胞进行基因表达谱分析

Downstream targets of Nm23-H1: gene expression profiling of CAL 27 cells using DNA microarray.

作者信息

Bosnar Maja Herak, Bago Ruzica, Gall-Troselj Koraljka, Streichert Thomas, Pavelić Jasminka

机构信息

Division of Molecular Medicine, Rudjer Bosković Institute, Zagreb, Croatia.

出版信息

Mol Carcinog. 2006 Aug;45(8):627-33. doi: 10.1002/mc.20243.

Abstract

The human nm23-H1 was discovered as a tumor metastasis suppressor based on its reduced expression in melanoma cell lines with low versus high metastatic potential. It encodes for one of two subunits of the nucleoside-diphosphate kinase. Besides its role in the maintenance of the cells NTP pool, nm23 plays a key role in different cellular processes. The role of nm23-H1 in these processes still has to be elucidated. Our goal was to identify Nm23-H1 downstream targets by subjecting Nm23-H1 overexpressing CAL 27 cells oral squamous cell carcinoma (OSSC) to microarray analysis. The genes with changed expression patterns could be clustered into several groups: transforming growth factor beta (TGFbeta) signaling pathway, cell adhesion, invasion and motility, proteasome machinery, cell-cycle, epithelial structural and related molecules and others. Based on the expression patterns observed we presume that nm23-H1 might have a role in OSSCs, which should be confirmed by future experiments.

摘要

人类nm23-H1最初是作为一种肿瘤转移抑制因子被发现的,这是基于它在低转移潜能与高转移潜能的黑色素瘤细胞系中表达降低。它编码核苷二磷酸激酶的两个亚基之一。除了在维持细胞NTP池方面的作用外,nm23在不同的细胞过程中也起着关键作用。nm23-H1在这些过程中的作用仍有待阐明。我们的目标是通过对过表达Nm23-H1的口腔鳞状细胞癌(OSSC)CAL 27细胞进行微阵列分析,来鉴定Nm23-H1的下游靶点。表达模式发生改变的基因可被聚类为几个组:转化生长因子β(TGFβ)信号通路、细胞黏附、侵袭与迁移、蛋白酶体机制、细胞周期、上皮结构及相关分子等。基于观察到的表达模式,我们推测nm23-H1可能在口腔鳞状细胞癌中发挥作用,这一点有待未来实验证实。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验