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许可因子Cdt1和Geminin在人类结肠癌中的表达。

Expression of the licensing factors, Cdt1 and Geminin, in human colon cancer.

作者信息

Bravou V, Nishitani H, Song S Y, Taraviras S, Varakis J

机构信息

Department of Anatomy and Histology-Embryology, School of Medicine, University of Patras, 26500 Rio, Patras, Greece.

出版信息

Int J Oncol. 2005 Dec;27(6):1511-8.

Abstract

Licensing of chromatin for replication is an evolu-tionarily conserved step in the control of cell division and genomic integrity. Proteins that participate in licensing have been recently documented to denote the proliferative state of cells and they have been proposed as diagnostic and prognostic markers in human cancer. Cdt1 was recently discovered as an important licensing factor, that is inhibited by Geminin. In the present study we analyzed Cdt1 and Geminin expression in human colon cancer. We showed that Cdt1 protein is highly expressed in human neoplastic lesions of the colon while its cell-cycle phase-specific expression profile appears preserved during human carcinogenesis. Similarly, Geminin, Cdt1's inhibitor, is also overexpressed in colon carcinomas and its expression correlates with significant clinicopathological parameters of the disease. Moreover, both Cdt1 and Geminin expression are severely downregulated upon differentiation of Caco-2 cells, an in vitro model of intestinal epithelial differentiation.

摘要

染色质复制许可在细胞分裂控制和基因组完整性方面是一个进化上保守的步骤。最近有文献记载,参与许可的蛋白质可指示细胞的增殖状态,并且它们已被提议作为人类癌症的诊断和预后标志物。Cdt1最近被发现是一种重要的许可因子,它受到Geminin的抑制。在本研究中,我们分析了人类结肠癌中Cdt1和Geminin的表达。我们发现,Cdt1蛋白在人类结肠肿瘤性病变中高度表达,而其细胞周期阶段特异性表达谱在人类致癌过程中似乎保持不变。同样,Cdt1的抑制剂Geminin在结肠癌中也过度表达,其表达与该疾病的重要临床病理参数相关。此外,在Caco-2细胞(一种肠上皮分化的体外模型)分化后,Cdt1和Geminin的表达均显著下调。

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