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MCM7转化簇的致癌活性。

Oncogenic activity of MCM7 transforming cluster.

作者信息

Luo Jian-Hua

机构信息

Jian-Hua Luo, Department of Pathology, University of Pittsburgh School of Medicine, 3550 Terrace Street, Pittsburgh, PA 15261, United States.

出版信息

World J Clin Oncol. 2011 Feb 10;2(2):120-4. doi: 10.5306/wjco.v2.i2.120.

Abstract

The miniature chromosome maintenance (MCM) complex is a group of proteins that are essential for DNA replication licensing and control of cell cycle progression from G1 to S phase. Recent studies suggest that MCM7 is overexpressed and amplified in a variety of human malignancies. MCM7 genome sequence contains a cluster of miRNA that has been shown to downregulate expression of several tumor suppressors including p21, E2F1, BIM and pTEN. The oncogenic potential of MCM7 and its embedded miRNA has been demonstrated vigorously in in vitro experiments and in animal models, and they appear to cooperate in initiation of cancer. MCM7 protein also serves as a critical target for oncogenic signaling pathways such as androgen receptor signaling, or tumor suppressor pathways such as integrin α7 or retinoblastoma signaling. This review analyzes the transforming activity and signaling of MCM7, oncogenic function of miRNA cluster that is embedded in the MCM7 genome, and the potential of gene therapy that targets MCM7.

摘要

微小染色体维持(MCM)复合体是一组对DNA复制许可以及细胞周期从G1期到S期进程的控制至关重要的蛋白质。最近的研究表明,MCM7在多种人类恶性肿瘤中过表达且发生扩增。MCM7基因组序列包含一簇微小RNA,已证明该簇微小RNA可下调包括p21、E2F1、BIM和pTEN在内的多种肿瘤抑制因子的表达。在体外实验和动物模型中,MCM7及其嵌入的微小RNA的致癌潜力已得到有力证明,并且它们似乎在癌症起始过程中协同作用。MCM7蛋白还是致癌信号通路(如雄激素受体信号通路)或肿瘤抑制通路(如整合素α7或视网膜母细胞瘤信号通路)的关键靶点。本综述分析了MCM7的转化活性和信号传导、嵌入MCM7基因组的微小RNA簇的致癌功能以及靶向MCM7的基因治疗潜力。

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