癌胚抗原受体在结直肠癌进展中的作用

O. Bajenova, E. Tolkunova, S. Koshkin, S. Malov, P. Thomas, A. Tomilin, S. O’Brien
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引用次数: 1

摘要

临床和实验数据表明,癌胚抗原(CEA, CD66e, CEACAM-5)在结直肠癌和其他类型上皮癌的肝转移形成中起关键作用。在cea诱导的转移中涉及的分子事件尚未明确。本小组首先从固定肝巨噬细胞(Kupffer细胞)表面克隆了cea结合蛋白的基因(CEAR)。在本研究中,为了进一步阐明CEAR在结直肠癌进展中的作用,在CEA-过表达和CEA-阴性的MIP-101结直肠癌细胞系中,CEAR在结直肠癌细胞中的表达被短发夹rna (short hairpin RNAs, shRNAs)抑制。数据显示,靶向抑制肿瘤细胞内源性CEAR可导致细胞侵袭性的改变。RT-PCR数据显示,在CEAR抑制的克隆中,E-cadherin、Snail、MMP-2和Oct-4的水平降低,这表明CEAR在上皮间质转化中起作用。用免疫缺陷小鼠脾内注射模型对CEAR抑制细胞系的肝脏致瘤活性进行了比较分析。该数据显示,与CEAR抑制相关的肿瘤进展减少。总之,本研究结果揭示了CEAR基因在调节结直肠癌细胞侵袭和进展中的新作用。
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The Role of the Carcinoembryonic Antigen Receptor in Colorectal Cancer Progression
Clinical and experimental data suggest that carcinoembryonic antigen (CEA, CD66e, CEACAM-5) plays a key role in the formation of hepatic metastasis from colorectal and other types of epithelial cancers. The molecular events involved in CEA-induced metastasis have yet to be defined. Our group first cloned the gene (CEAR) for CEA-binding protein from the surface of fixed liver macrophages, (Kupffer cells). In this study to further elucidate the role of CEAR in colorectal cancer progression, its expression in colorectal cancer cells was suppressed by short hairpin RNAs (shRNAs) in CEA-overexpressing and CEA - negative MIP-101 colorectal cancer cell lines. The data show that targeted suppression of endogenous CEAR in tumor cells resulted in changes in cell invasiveness. RT-PCR data indicated reduced levels of E-cadherin, Snail, MMP-2, and Oct-4 in the clones with suppressed CEAR suggesting a role in the epithelial mesenchymal transition. The comparative analysis of tumorigenic activity to the liver of the cell lines with suppressed CEAR has also been conducted using an intrasplenic injection model in immuno-deficient mice. This data shows a decrease in tumor progression associated with CEAR suppression. In summary the results of this study revealed a novel role for CEAR gene in the regulation of colorectal cancer cell invasiveness and progression.
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